COCAINE DRUG TEST (COC DRUG TEST)

WHY A COCAINE DRUG TEST IN THE WORKPLACE?

Businesses and government agencies around the world are facing a myriad of problems regarding drug use, specifically cocaine drug use, by employees in the workplace.  Some have chosen to have their employees sent to a clinic to take a cocaine drug test, or a multi drug test, and some have chosen to conduct the drug test(s) on site.

What kind of business would consider conducting drug tests for their employees?  There are many reasons to require a cocaine drug test, or maybe even a multi drug test for employees.  Most private companies are not required to give drug tests, multi drug tests, alcohol and drug tests, or a specific drug test like a cocaine drug test.  However, there are several reasons why some companies, large and small, would administer drug tests, like the cocaine drug test, to their employees.  First of all, safety-sensitive industries that are regulated by certain federal or state agencies must include testing of employees, such as the cocaine drug test, or in some cases, multi drug tests. This would involve drug testing to avoid violation of OSHA and state occupational safety laws.  Also, any industry connected to transportation of goods or services must consider cocaine drug tests for the safety of their employees, customers, and the general populace, not to mention avoiding violation of intra state transportation laws.  This would include cocaine drug tests, or multi drug tests, for jobs such as airline/maritime pilots and personnel, trucking company drivers, railroad employees, taxi cab drivers, delivery personnel, mass transit drivers, as well as those connected to military and government agencies.  Of course those companies employing professionals in the health field need to consider drug testing, for the safety of their employees and patients, and a drug test like the cocaine drug test is popular in the construction industry too, in addition to multi drug testing in pipeline and hazardous materials jobs.  As one can see, the list is long for workplace considerations on such drug tests as the cocaine drug test.

Then there are those companies who must consider employee drug testing, like a cocaine drug test, in order to comply with workmen’s compensation requirements.  Many employers who drug test their employees, as in a cocaine drug test or multi drug tests, qualify their company for certain discounts on insurance premiums that involve safety in the workplace.  Other reasons for offering a cocaine drug test, or multi drug test, would be to avoid legal liability.  If other employees, or customers, were harmed for any reason through cocaine drug use or other multi drug use by an employee, the company would be liable for damages.  Lastly, it is cost effective for a business, whether large or small, to regularly administer drug tests like a cocaine drug test, in order to save money in the long run.  Studies have shown that billions of dollars a year are spent by companies on such things as lost productivity due to absences and tardies, costs due to workplace accidents, and high workmen’s compensation claims.  In addition, these cocaine drug tests, or use of multi drug tests, can be administered for pre-employment screening, as part of the hiring process, to ensure against future problems due to regular drug use in the workplace.

WHY ARE MORE EMPLOYERS IMPLEMENTING COCAINE DRUG TESTING PROGRAMS?

Requiring drug tests like a cocaine drug test has become a common practice among many businesses, companies, and government agencies.  Sports organizations also routinely test athletes for illegal drug substances, like the cocaine drug, or performance enhancing drugs.  There are a multitude of facilities, such as doctor’s offices, hospitals, occupational health clinics, and individual laboratories that are directly involved in cocaine drug testing programs, and/or multi drug testing programs.  Employers can make a difference using cocaine drug testing procedures.  The cocaine drug testing program, or any multi drug test program, will act as a road map for managers and supervisors.    Current research indicates that more than 70% of illegal drug users are employed in full and part-time jobs in the U.S alone.  Consequently, the result is a large impaired portion of the national workforce.  When an employee is impaired on the job, the company has not only lost one productive employee, but in fact has dramatically reduced the productivity of all the other workers who they interact with. Drug use in the workplace has a ripple effect. Not only is productivity reduced, but company morale is negatively impacted, causing good employees to leave the company to avoid drug impaired co-workers.   For the typical employer, that means unhealthy employees, unsafe working conditions, loss of productivity, smaller profits, more accidents, higher medical claims expenses, and a host of other negative effects for the employer and the employees.  Workers may also be coming to work more stressed out which can play a role in increased drug abuse.  The desire for businesses to have more cocaine drug testing or multi drug testing programs in the workplace has been amplified in recent years due to job insecurity and a trend toward working longer hours by their employees. Companies can minimize the chance of having to deal with a serious job performance problem in the workplace, and in the process support a better quality of life for employees, by implementing a cocaine drug testing, or a multi drug testing program in their company.   Use of the cocaine drug test, or a multi drug test program, will reinforce the message to employees and customers that a positive work environment is a high priority.  To combat the drug abuse problem, many employers offer EAP’s (employee assistance programs) that include cocaine drug use counseling.

HOW DOES A COCAINE DRUG TEST WORK?

A cocaine drug test, or a multi drug test, can be administered on site or done in a laboratory.  The easy-to-use cocaine drug test, or any combination multi drug test, manufactured and distributed by Diagnostic Automation/Cortez Diagnostics, Inc., are some of the best quality drug tests available on the market today.   These simple-to-use drug testing kits do not require any professional assistance, which makes them perfect to be used at workplaces anytime.  The cocaine drug test is an immuneochromatography-based one step in vitro test.  The cocaine drug test is designed for qualitative determination of cocaine’s metabolite, benzoylecgonine in human urine specimen above a cutoff level of 300 ng/ml.   Diagnostic Automation/Cortez Diagnostics, Inc. also offers multi drug tests which can detect cocaine and any other combination of drugs (and alcohol) through multi panel drug tests, from 2 panel to 9 panel drug tests.  For customized cutoff level cocaine drug tests, or multi panel drug tests, please contact our Customer Service Department. The cocaine drug test (COC Drug Test) is available in multi-panel, cassette, strip, or cup format.  The multi panel drug testing kits are also available in cassette, strip, or cup format.

When it comes to workplace drug testing, the usage of drug testing kits becomes imperative. It is not only because of their ease of use but also for accurate and quick results.  The results of the cocaine drug test or multi drug test are highly reliable and accurate.  Moreover, these drug test kits do not take more than 5 minutes to show the results, making it possible, if necessary, for a business or public organization to take quick action against drug usage.   Implementing a drug feee workplace program takes thoughtful consideration of what the business or organization is trying to accomplish, how they want to accomplish it, how much it will cost, and how much it will save.  In offering top quality – cost effective cocaine drug tests and multi drug tests, Diagnostic Automation/Cortez Diagnostics, Inc. establishes itself as an integral part of any business and organization’s commitment to implement effective workplace drug testing programs and in the long run, be part of the solution in decreasing workplace drug abuse problems.

DENGUE ELISA KITS – DENGUE RAPID TESTS – FREQUENTLY ASKED QUESTIONS

Los Angeles-based Diagnostic Automation/Cortez Diagnostics, Inc., a leading manufacturer and distributor of medical test kits in the U.S. and throughout the world, offers a wide variety of Dengue ELISA Kits and Dengue Rapid Tests to its customers.  Contained on our web site are frequently asked questions from our customers about Dengue ELISA Kits and Dengue Rapid Tests.   Below is a sample of some of those questions that we feel will assist any hospital, clinic, or health organization in making a decision about the proper medical testing equipment for your particular population.  Please see the product inserts for more specific information on each product, or contact our Customer Service Department for any further information on these Dengue ELISA Kits, Dengue Rapid Test Kits, or any other medical testing products.

POPULAR DENGUE ELISA KITS – FAQ

Available Dengue ELISA Test Kits:

Dengue Antibody IgG/IgM ELISA Kit  (#8115-3)

Dengue Antibody – IgG ELISA Kit  (# 8116-3)

Dengue Antibody IgM ELISA Kit  (#8117-3)

What serotypes does the Dengue ELISA Kit use?

The Dengue ELISA kits contain micro wells that are coated with purified dengue virus antigen from vero cell cultured type 1-4 dengue.

What is the sensitivity and specificity of the Dengue ELISA Kits?

Dengue IgG/IgM ELISA test is 100% and 78%;  Dengue IgG ELISA test is 100% and 96%; Dengue IgM ELISA test is 100% and 86%.  See package inserts for details on Dengue ELISA test kits.

Why are 2 wells per sample needed on the Dengue ELISA Kits?

In addition to Dengue recombinant antigen, samples on the Dengue ELISA tests are screened with a normal cell antigen.  This step on the Dengue ELISA test optimizes the specificity by helping eliminate any false positives that may occur in the Dengue ELISA test because of non-specific interactions of the antigen with the sample.

How many unknown samples can be tested with the Dengue ELISA Kit?

Up to as many as 44 samples can be tested on the Dengue ELISA Kit.

What is the storage of the Dengue ELISA test Kit?

Storage of Dengue ELISA Kits range from 2 – 8 degrees celsius.

What is the shelf life of the Dengue ELISA test kits?

Storage time of the Dengue ELISA test kits is 12 months from manufacture date.

What is the cpt code of Dengue ELISA kit?

Generally there is a common generic code available for these Dengue ELISA tests- Dengue IgG/IgM ELISA test, Dengue IgG ELISA test, and Dengue IgM ELISA test.  For the latest specific code number, please contact our Customer Service Department.

Do you also have Dengue NS1 ELISA kits?

Yes, we offer Dengue NS1 ELISA kit (#8404-25) and Dengue NS1 Rapid Test (#173110-25).  Contact our Customer Service Department for more information.

Do you distribute Dengue NS1 Rapid Tests?

We offer a fast and easy-to-use Dengue NS1 Antigen Rapid Test (#173110-25).  See our Customer Service Department or product inserts for more information.

CONVENIENT AND EASY-TO-USE DENGUE RAPID TEST – FAQ

Dengue IgG/IgM Antibody Rapid Test (#173106L-25)

What serotypes does the Dengue Rapid Test detect?

This Dengue Rapid Test is a new generation immunochromatographic test using recombinant dengue viral antigens of all four serotypes (DENV 1-4) to detect specific antibody response. By using a mixture of highly purified dengue proteins, the Dengue Rapid Test is able to detect all 4 Dengue serotypes.

What principle is used in the Dengue Rapid Test?

This Dengue Fever Rapid Test is a qualitative immunochromatographic test for the simultaneous detection of IgM and IgG antibodies to dengue virus in human serum, plasma, or whole blood.

How effective is the Dengue Rapid Test in detecting Dengue fever in patients?

A high proportion of dengue virus infections can be detected swiftly and easily using a Dengue Rapid Test.  The Dengue Rapid Test can help to diagnose active dengue infections from the very first day fever appears.  In facilitating early diagnosis by using this Dengue Rapid Test, therapy and monitoring can begin much earlier, reducing the risk of severe complications.

What is the storage of the Dengue Rapid Test Kit?

Serum/Plasma of the Dengue Rapid Test Kit may be stored at 2 – 8 degrees celsius up to 3 days.  For long-term storage, freeze the specimen at -20 degrees celsius for 3 months, or -70 degrees celsius for longer periods.  See product insert of Dengue Rapid Test Kit for more details.

What is the total time it takes to process a sample on the Dengue Rapid Test?

Time to process samples on Dengue Rapid Test Kit is approximately 30 minutes.  Once the Dengue Rapid Test sample is applied, results can be obtained within 20 minutes.

DENGUE NS1 ELISA KIT and DENGUE NS1 RAPID TEST -  FREQUENTLY ASKED QUESTIONS

Dengue fever is a worldwide health problem, and in epidemic proportions in some countries.  The World Health Organization estimates that annually, 50-100 million people are infected worldwide with the dengue virus.   Studies have shown that early detection of Dengue NS1 virus using tests like the Dengue NS1 ELISA test and Dengue NS1 Rapid test can help in early confirmation, clinical treatment, and control of dengue viral infections.  To address this problem,  Los Angeles-based Diagnostic Automation/Cortez Diagnostics, Inc., a leading manufacturer and distributor of medical test kits in the U.S. and throughout the world, offers two very popular Dengue NS1 test kits — Dengue NS1 ELISA Kit and Dengue NS1 Rapid Test that detect Dengue NS1 (non-structural protein 1) of Dengue virus.  The Dengue NS1 ELISA test and the Dengue NS1 Rapid Test are effective new diagnostic tools for early diagnosis of dengue virus infection.  Below are some of the frequently asked questions surrounding these products.

NEW PRODUCT – DENGUE NS1 ANTIGEN ELISA KIT – FAQ

Dengue NS1 Antigen ELISA KIT  (#8404-25)

Is the Dengue NS1 ELISA kit easy to use?

The Dengue NS1 ELISA Kit is an excellent assay that contains a high level of sensitivity and specificity in detecting the NS1 antigen of Dengue virus.  The Dengue NS1 ELISA Kit is a rapid and reliable Dengue ELISA kit that contains sufficient reagents for one plate of 96 wells.  The user-friendly Dengue NS1 ELISA Kit contains components that are highly effective and the Dengue NS1 ELISA Kit has easy-to-read controls to determine positive or negative results.

How long is the incubation time of the Dengue NS1 ELISA Kit?

Total incubation time of the Dengue NS1 ELiSA test is approximately 2 hours (60-30-20).  Incubation procedures of the Dengue NS1 ELISA test kit are easy to follow.  Clear instructions for specific Dengue NS1 ELISA test procedures in specimen collection and preparation are found in the Dengue NS1 ELISA kit product insert which should help with your specific needs.

What is the total time it takes to process a sample on the Dengue NS1 ELISA kit?

Total time for the Dengue NS1 ELISA Test to be performed is approximately 250 minutes.

What principle is used in the Dengue NS1 ELISA test kit?

Dengue NS1 Antigen ELISA test uses the two-step sandwich type immunoassay to detect low levels of NS1 in serum.

What is the storage of the Dengue NS1 ELISA kit?

The samples of the Dengue NS1 ELISA kit may be stored at 2-8 degrees celsius for up to 7 days, or frozen at -20 degrees celsius or lower for up to 30 days.  To maintain long-term longevity of the serum on the Dengue NS1 ELISA kit, store at -70 degrees celsius.  Avoid repeated freezing and thawing of samples on Dengue NS1 ELISA kit.

What is the shelf life of the Dengue NS1 ELISA kit?

Shelf life of the Dengue NS1 ELISA test is 12 months from the manufacture date.

Do you also distribute Dengue ELISA Kits for IgG and IgM antibodies?

Yes, we offer three Dengue ELISA kits – Dengue ELISA IgG/IgM kit, Dengue ELISA IgG kit, and Dengue ELISA IgM kit.  In addition, an easy-to-use and reliable Dengue Rapid Kit is available.

NEW PRODUCT – DENGUE NS1 ANTIGEN RAPID TEST – FAQ

Dengue NS1 Antigen Rapid Test  (#173110-25)

What is the total time it takes to process a sample on the Dengue NS1 Rapid Test?

Depending on how many samples are collected, testing of Dengue NS1 Antigen Rapid Test should be done immediately after collection of serum.  Serum collection and reading results on Dengue NS1 Antigen Rapid Test can be performed in approximately 30 minutes.  Caution: do not interpret results of the Dengue NS1 Rapid Test more than 45 minutes after serum collection as this may lead to erroneous results.

What is the storage of the Dengue NS1 Rapid Test?

The sealed pouch and Chase Buffer of the Dengue NS1 Rapid Test are designed to be stored at room temperature (22 – 30 degrees celsius) for the duration of their shelf life.  Exposure to temperatures over 30 degrees celsius can impact the performance of the Dengue NS1 Rapid Test and should be minimized.

What principle is used in the Dengue NS1 Antigen Rapid Test?

The Dengue NS1 Antigen Rapid Test is a qualitative, membrane based immunoassay for the detection of NS1 antigen in human serum.  The Dengue NS1 Rapid Test membrane is pre-coated with a NS1 specific antibody on the Dengue NS1 Rapid Test line region and utilizes a separate control to assure assay flow and performance.  During testing, the Dengue NS1 Antigen Rapid Test sample is added directly to the sample region on the Dengue NS1 Rapid Test and the test is placed into a well containing 3 drops of buffer. The buffer and serum mix and interact with NS1-specific monoclonal antibodies conjugated to gold nano particles.  The solution in the Dengue NS1 Rapid Test migrates upward on the membrane to react with the anti-NS1 antibody on the membrane.  If NS1 antigen is present, a red line will appear at the Dengue NS1 Rapid Test line.

What is the sensitivity and specificity of the Dengue NS1 Antigen Rapid Test?

The relative high sensitivity in detecting patients with primary infections and the overall high specificity of the Dengue NS1 Antigen Rapid Test make it well suited for the early detection of dengue virus.  Recent studies have shown the Dengue NS1 Antigen Rapid Test as having a sensitivity of 85% to 89% and a specificity of nearly 98%.  The diagnostic sensitivity of the Dengue NS1 Antigen Rapid Test is significantly enhanced if used in a combination antigen and antibody testing approach.

Dengue Rapid Tests

Los Angeles-based Diagnostic Automation/Cortez Diagnostics, Inc., a leading manufacturer and distributor of Dengue Fever Rapid Tests, offers an easy-to-use Dengue Rapid Test to identify the dengue virus.  This Dengue Fever Rapid Test is a qualitative test for the detection of IgM and IgG antibodies to dengue virus in human serum, plasma or whole blood. The Dengue rapid test provides a differential detection of anti-dengue IgM and anti-dengue-IgG antibodies.  The Dengue Rapid Test can be used for the presumptive distinction between a primary and secondary dengue infection.   A high proportion of dengue virus infections can be detected swiftly and easily using a Dengue Rapid Test.  The Dengue Rapid Test can help to diagnose active dengue infections from the very first day fever appears.  In facilitating early diagnosis by using this Dengue Rapid Test, therapy and monitoring can begin much earlier, reducing the risk of severe complications.  Early and prompt diagnosis with the Dengue Rapid Test can facilitate vector control activities in the community so as to mitigate further transmission.  Also, the expanded use of accurate Dengue Rapid Tests provides important data on the epidemiology and health burden of dengue and in doing so can inform and guide public health policy.

According to the World Health Organization’s 2009 Report, “Dengue is the most rapidly spreading mosquito-borne viral disease in the world.  In the last 50 years, incidence has increased 30-fold with increasing geographic expansion to new countries. . . . An estimated 50 million dengue infections occur annually and approximately 2.5 billion people live in dengue endemic countries.”  Because of the vast implications of these findings, it is essential that early detection of dengue fever, like those offered using Dengue Rapid Tests, is vitally important for the prompt care and treatment of infected individuals. Timely, sensitive, and easy to use, the Dengue Rapid Tests are essential for early detection and identification of the infection so that treatment may be started without delay.

DENGUE RAPID TEST – NOTABLE FEATURES

The Dengue Rapid Test, or OneStep Dengue RapiCardTM InstaTest, is a immunochromatographic assay for the simultaneous detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum or plasma. The assay is used as a screening test for Dengue viral infection and as an aid for differential diagnosis of primary and secondary infections in conjunction with other criteria.  This Dengue Rapid Test is a new generation immunochromatographic test using recombinant dengue viral antigens of all four serotypes to detect specific antibody response. This convenient and easy-to-use Dengue Rapid Test is for in-vitro diagnostic use only.  The Dengue Fever Rapid Test provides an excellent methodology for specifically detecting anti-dengue IgG and IgM antibodies. The presence of high titers of IgG antibodies on the Dengue rapid test does not interfere with the detection of IgM antibodies in the sample.  By using a mixture of highly purified dengue proteins, the Dengue rapid test is able to detect all 4 Dengue serotypes.

Serum, plasma or whole blood samples may be used with this Dengue rapid test. When a specimen is added to the Dengue rapid test, IgG and IgM antibodies in the specimen sample react with blue particles coated with dengue envelope proteins. As this specimen/particle mixture migrates along the length of the Dengue rapid test, the anti-dengue IgG or IgM antibody particle complex is captured by the relevant IgG and/or IgM test bands located in the Dengue rapid test device window causing a pale to dark blue band to form at the IgG or IgM region of the test device window. The intensity of the bands on the Dengue rapid test will vary depending upon the amount of antibody present in the sample. The appearance of any color in a specific Dengue rapid test region (IgG or IgM) should be considered as positive for that particular antibody type (IgG or IgM).  A red procedural control line should always develop in the Dengue rapid test device window to indicate that the Dengue rapid test has been performed properly.

DENGUE RAPID TEST – RELATED PRODUCTS

Diagnostic Automation/Cortez Diagnostics, Inc. has been a leader in the development of infectious disease rapid tests for more than 20 years.  The use of tests like this Dengue Rapid Test, as a first-line test for the screening and treatment of dengue-infected patients, could help to accelerate the diagnosis of dengue fever in clinical diagnostic laboratories.  Rapid and easy diagnosis of dengue infection using the Dengue Rapid Test can assist patient triage and care management.  This Dengue Fever Rapid Test is available in cassette format only.  For more information on this Dengue Rapid Test, please contact Customer Service.

Other products are also available in the fight to diagnosis and treat the dengue virus.  One highly effective Dengue Rapid Test is the fairly new Dengue NS1 Rapid Test.  The Dengue NS1 Rapid Test is a chromatographic immunoassay for the qualitative detection of non-structural protein 1 (NS1) antigens in whole blood, serum, or plasma.  Along with this Dengue Rapid Test is the newly arrived Dengue NS1 Antigen ELISA Kit which is an Enzyme Linked Immunosorbent Assay for the detection of dengue virus in human serum even prior to the presence of IgM or IgG antibodies.   Lastly, three Dengue ELISA Kits are available that specifically detect and identify IgG, IgM, and combination IgG/IgM antibodies respectively in human serum.  For more information on any of these Dengue Rapid Tests or Dengue ELISA Kits, please contact our Customer Service Department.

Serology Tests

Serology tests are conducted for the scientific study of blood serum and other bodily fluids.  Serology tests are performed for several purposes.  One use of a Serology test is for diagnostic purposes when an infection is suspected.  A Serology test can identify certain antibodies in serum that are formed in response to an infection against foreign proteins (for example from blood transfusion), or to one’s own proteins (for instance, autoimmune disease).  A serology test can also determine if there has ever been exposure to a particular microorganism in the past, not necessarily indicating a current infection.

A serology test additionally can be employed to detect current active infection, or past infection, in people who are at risk for reactivation of infection (such people with suppressed immune systems, organ transplants, HIV, Syphilis, etc.).  In addition, Serology tests are often used by epidemiologists to determine the prevalence of a disease in a certain segment of population.  These serology tests are sometimes performed by random, anonymous sampling.  Serology tests are also important tools that may be used forensically, specifically to reveal a piece of evidence for a crime report, or court case.

Los Angeles-based Diagnostic Automation/Cortez Diagnostics, Inc. is pleased to offer a wide range of serology tests for the quick and reliable measurement of specific antibodies in human serum samples.  Some of these serology tests are latex agglutination tests (latex fixation) which use latex particles as passive carriers where particles clump together following the addition of the antibody on the serology test.

•     One such serology test is the Latex ASO Serology Test which is a serology test intended for the qualitative and semi-quantitative measurement of antibodies to streptococcal exoenzymes in human serum.  Packaged in convenient boxes of 50 serology tests, this (antistreptolysin O) ASO serology test is easy to use and cost effective for hospitals, doctors’ offices, and laboratories worldwide who need quick and easy test results for individual patients, or testing for a large segment of the population.

•        Another popular serology test is the CRP Serology Test that is used for the qualitative and semi-quantitative measurement of C-reactive protein in human serum.  This simple and easy-to-use CRP Serology Test is based on the principle of the latex agglutination assay described above and detects protein markers for inflammation in the body.   The major advantage of this serology test is the rapid three (3) minute reaction time.  Packaged in boxes each of 100 serology tests, this top quality serology test is convenient for any testing site diagnosing patients with acute and chronic inflammatory conditions.

•        A third latex serology test is the Mono Serology Test which is intended to be used for the qualitative and semi-quantitative determination of human heterophile antibodies associated with Infectious Mononucleosis (IM).  Ordering these serology tests is easy and convenient.  The Mono Serology Tests are distributed in boxes of 50 serology tests and are to be applied in-vitro diagnostic use only.  These Mono Serology Tests are known for their high sensitivity and specificity.

•        The fourth latex serology test is entitled the RF Serology Test which is intended for the qualitative and semi-quantitative measurement of RF (rheumatoid factor) in human serum.  The frequent occurrence of rheumatoid factors in rheumatoid arthritis makes them useful for diagnoses, like those employed by this serology test, and subsequent monitoring of the disease.   The major advantage of this RF Serology Test is rapid performance (3 minute reaction time) and lack of heterophile antibody interference.  Interested parties can obtain these useful and reliable serology test kits each containing 100 boxes.

•        The fifth latex serology test is the SLE Serology Test which is used as an aid in the diagnosis of Systemic Lupus Erythematosus (SLE) through the detection and quantitation of serum anti nucleoprotein factors associated with SLE.  The principle of the SLE Serology Test is based on the agglutination reaction between latex particles coated with DNP being brought into contact with a serum, which contains antinuclear antibodies.  A visible agglutination on the serology test indicates a positive reaction.  The reaction time for this occurrence on this serology test is one minute.  These top quality serology test kits are packaged in 50 boxes each kit.

The last superior quality serology test manufactured and distributed by Diagnostic Automation/Cortez Diagnostics, Inc. is the convenient and highly effective RPR Serology Test which is a Rapid Plasma Reagin -RPR Serology Test that is a non-treponemal flockulation test used for qualitative and semi-quantitative determination of reagin antibodies in serum or plasma from persons with syphilis.  The antigen used in the serology test kit is a modification of VDRL antigen, which contains micro-particulate charcoal to enhance the visual difference between a positive and negative result.  If a specimen on this serology test contains reagin, flocculation occurs with a coaglutination of carbon particles contained in the antigen suspension, which appears as black clumps.  Non-reactive specimens on the serology test appear as an even light gray homogenous suspension.  These safe and cost-effective serology test kits are distributed in packages of 100 or 500 boxes, and are for in-vitro diagnostic use only.  Reactive RPR Serology test specimens should be subjected to further confirmation testing.

Well, there they are — our products for serology tests.  Diagnostic Automation/Cortez Diagnostics, Inc. in its continual endeavor to provide top quality products to laboratories, hospitals, doctors’ offices, health clinics, law enforcement facilities, judicial courts, and other interested sites around the world, is proud to manufacture and distribute such superior products that help diagnose and subsequently aid in a line of treatment for the health and welfare of citizens around the globe.

RELATED PRODUCTS

Diagnostic Automation/Cortez Diagnostics, Inc. is a USA based company manufacturing and distributing Rapid Tests (HIV Rapid Test, Drug Tests or Drugs of Abuse Rapid Tests, Cardiac Rapid Tests, Allergy Rapid Tests, Cancer Rapid Tests, Pregnancy Rapid Tests, Urine Reagent Strips, etc.), ELISA Test Kits (Autoimmune diseases ELISA Kit, Cardiac Markers, Allergy ELISA kits, HIV ELISA kits, etc.), IFA Kits (Autoimmune diseases IFA Kits, Autoimmune Disease Kits, Bacterial Disease IFA Kits, etc.), Chemilluminescence immuno assays (Infectious Disease kits, Fertility Assays/CLIA kits, Diabetes Assays/CLIA kits, Cardio-Vascular/CLIA kits, Tumor Marker Assays kits, etc.), and ELISA readers – ELISA washers and Serology test kits.

For more information about these serology tests or any other products offered by Diagnostic Automation/Cortez Diagnostics, Inc. please contact our Customer Service Department.  

MALARIA RAPID TEST

Malaria Rapid Test (Pan-LDH) WB (Cassette)

Malaria Rapid Test (P.f./Vivax) WB (Cassette)

Los Angeles based Diagnostic Automation/Cortez Diagnostics, Inc. offers two convenient, reliable, and inexpensive Malaria Rapid Tests:   One Malaria Rapid Test is for Pan-LDH antigens.  This Malaria Rapid Test can detect all four species of malaria Plasmodium falciparum, Plasmodium vivax, Plasmodium oval, and Plasmodium malaria.  This Malaria Rapid Test is for the qualitative detection of one or more of the known Malaria species: P. falciparum, p. vivax, P. oval, and/or P. malaria by detecting lactate dehydrogenase (LDH) in human blood.  This Malaria Rapid Test is for in vitro diagnostic use only.  The second easy-to-use Malaria Rapid Test is for detection of pf and pv antigens only. This particular Malaria Rapid Test is a rapid, qualitative test for the detection of Plasmodium falciparum and/or Plasmodium vivax in whole blood.  This Malaria Rapid Test is also for in-vitro diagnostic use.

WHY HAVE A MALARIA RAPID TEST?

Malaria is a serious, sometimes fatal infection of red blood cells caused by the bite of a carrier mosquito.  Symptoms include high fever with shaking chills, heavy sweating, fatigue, headache, abdominal pain and nausea and vomiting.  Malaria now occurs in more than 90 countries worldwide, and it is estimated that there are over 500 million clinical cases and 2.7 million malaria-caused deaths per year.  Prompt and accurate diagnosis like that obtained using a Malaria Rapid Test, followed by effective treatment, is currently the main malaria control strategy.  Early diagnosis like that offered through the malaria rapid test, and prompt, effective treatment of uncomplicated malaria is critical to prevent severe disease, death and malaria transmission.  Malaria Rapid tests play an important role in many countries who have health clinics that need to perform on-site tests in various field conditions, and Malaria Rapid Tests are often used by community health workers in areas where malaria microscopy is not always immediately available.  Clinicians should be aware that certain hospitals and laboratories may offer a malaria rapid test, which can aid in the rapid diagnosis of malaria and result in prompt therapeutic intervention.  Since early diagnosis is essential, strategies to improve access to treatment at the community level have been endorsed by WHO.  The World Health Organization’s evaluation of malaria rapid tests showed substantial improvement in test performance on nearly all of the malaria rapid tests evaluated.   In addition, an ever-increasing number of travelers each year who visit various tropical countries return with malaria infections. The malaria rapid tests are regarded as accurate tests to detect any species of malaria infection for this population too.

SAFE AND EFFECTIVE MALARIA RAPID TESTS

Diagnostic Automation/Cortez Diagnostics, Inc. distributes these user-friendly malaria rapid tests throughout the world.  Because malaria is a curable disease, provided the patients get an early diagnosis and prompt treatment, our malaria rapid tests are simple and the procedures to perform both malaria rapid tests can be done easily and results obtained quickly.  Malaria presents a diagnostic challenge to many infected areas throughout the world.  In these areas, rapid detection of the malaria parasites, as that offered in a malaria rapid test, and early treatment of infection remain the most important goals of disease management.  Countries with large population segments susceptible to malaria infection, have greater choice for quality malaria rapid tests like those offered by our company.  Malaria rapid tests are more suited to health workers in situations where health services are deficient or absent.  These malaria rapid tests have been assessed as safe and effective as diagnostic tools for community health workers, making these malaria rapid tests extremely useful, especially in rural areas.  Previous studies have confirmed their high sensitivity and specificity under field conditions. Therefore, the malaria rapid test can be used as a valuable tool for the rapid screening of malaria.

Diagnostic Automation/Cortez Diagnostics is pleased to offer these two formats of the Malaria Rapid Test — the Malaria Rapid Test for Pan-LDH antigens and a Malaria Rapid Test for pf and pv antigens.  For more information regarding these Malaria Rapid Tests, please contact our Customer Service Department.  These Malaria Rapid Tests are available in cassette format only.

RELATED PRODUCTS

Diagnostic Automation/Cortez Diagnostics, Inc. is a USA based company manufacturing and distributing Rapid Tests (HIV Rapid Test, Drug Tests or Drugs of Abuse Rapid Tests, Cardiac Rapid Tests, Allergy Rapid Tests, Cancer Rapid Tests, Pregnancy Rapid Tests, Urine Reagent Strips, etc.), ELISA Test Kits (Autoimmune diseases ELISA Kit, Cardiac Markers, Allergy ELISA kits, HIV ELISA kits, etc.), IFA Kits (Autoimmune diseases IFA Kits, Autoimmune Disease Kits, Bacterial Disease IFA Kits, etc.), Chemilluminescence immuno assays (Infectious Disease kits, Fertility Assays/CLIA kits, Diabetes Assays/CLIA kits, Cardio-Vascular/CLIA kits, Tumor Marker Assays kits, etc.), and ELISA readers – ELISA washers and Serology test kits.

Please contact our Customer Service Department for information about any of these Rapid Tests, ELISA Test Kits, CLIA Kits, IFA Kits, or any other drug testing products of interest.

CHLAMYDIA RAPID TEST KITS

CHLAMYDIA MALE RAPID TEST

CHLAMYDIA FEMALE RAPID TEST

Los Angeles based Diagnostic Automation/Cortez Diagnostics, Inc. is pleased to offer a OneStep Chlamydia RapiCard™ InstaTest which is a rapid immunoassay for direct qualitative detection of Chlamydia trachomatis antigen in swab specimens.  The Chlamydia Rapid Test is an easy-to-use test for point-of-care diagnosis of a chlamydia infection.  The Chlamydia Rapid Tests are quick and simple tests individually designed for either female or male patients looking for a reliable type of STD Test Kit.

Chlamydia, caused by the bacterium Chlamydia trachomatis, is regarded as one of the most common sexually transmitted diseases (STD’s) in both men and women today, most frequently affecting the young population between the ages of 16-24 years.  Because the chlamydia infection has no symptoms, the rate of infection can be nearly twice as that reported. If caught early, by using such tests as Chlamydia Rapid Test, chlamydia is easily cured with antibiotics.  That is why annual screening using tests like the Chlamydia Rapid Test is highly recommended, especially for all sexually active men and women.  Retesting with the Chlamydia rapid test is also advised three months after infection has been detected.  Because of these facts, annual use of a Chlamydia Rapid Test Kit, or STD Chlamydia Rapid Test Kit, is recommended to safeguard against further STD infections, such as the chlamydia infection.

Chlamydia is known as the “silent disease” because symptoms of Chlamydia infection often go unnoticed before damage is done to the infected.  Although Chlamydia can be detected using tests like the Chlamydia Rapid Test and cured with antibiotics, studies have shown that if left untreated, serious complications can arise including infertility in both women and men.  Because of these facts, Chlamydia screening with tests like the Chlamydia Rapid Test Kit is recommended on a regular basis, especially for the young population.  If positive results appear, visiting a doctor for clinical lab testing is a must.  After cured, once a year visit to the doctor is advised for a Chlamydia Rapid Test, or an STD Test, as it is possible to be reinfected with the disease even after Chlamydia Rapid test treatment.  If rapid STD test kits like this Chlamydia Rapid Test kit are not readily available to clinics, labs, and doctors around the world, it will be difficult to stem the tide of increasing chlamydia infection globally.  This Chlamydia Rapid Test Kit for both men and women is a serious way forward in diagnosing, treating, and curing chlamydia infections.

CHLAMYDIA RAPID TEST – STD TEST KIT FOR FEMALES

Recent studies have shown that in the United States alone, less than 40% of young women, ages 15 to 25, who are sexually active, were screened for chlamydia infection, using simple tests like this Chlamydia Rapid Test.  If caught early, by using an STD test kit like this Chlamydia Rapid Test, chlamydia is easily cured with antibiotics.  That is why annual screening using tests like this Chlamydia Rapid Test Kit is important for not only women in the United States but those around the world.  Not doing so, allows this “silent disease” to cause sometimes irreversible damage to the female patient.  Infections can spread into the uterus or fallopian tubes and cause pelvic inflammatory disease.  Undetected infections in the upper genital tract can also damage the uterus and surrounding tissues, causing chronic pain, infertility and potentially fatal ectopic pregnancies.  Studies have revealed also that chlamydia may make a woman more vulnerable to HIV infections.  It is critical that women avail themselves of tests like this Chlamydia Rapid Test and that health care professionals around the world be aware of the importance of sexually active young female patients getting STD tests like the Chlamydia Rapid Test on a regular basis.  Of course, retesting with Chlamydia Rapid Test after three to six months of infection is highly recommended to prevent further infection.  The Chlamydia Rapid Test contains non-invasive and easy-to-use components for convenient and practical treatment of female patients.

CHLAMYDIA RAPID TEST- STD TEST KIT FOR MALES

Recent studies have shown that chlamydia in men is more common than other male sexually transmitted diseases, with millions of newly reported cases each year.  Chlamydia in men, especially men under 25 who have had more than one partner within the prior year, affects a huge portion of the population, and sexually active young men should make a point of having frequent chlamydia tests like this Chlamydia Rapid Test.  Because the disease is asymptomatic in both men and women, it is important men get an STD test like this Chlamydia Rapid Test in order to successfully treat the infection on the spot.  The most common site of the chlamydia infection in men is inside the urethra, the tube through which men urinate and pass sperm.  If symptoms show in men, they may include discharge or pain when passing urine.  If untreated with a test like the Chlamydia rapid test, it may be a cause of reduced fertility.  Without an effective Chlamydia rapid testing program in particular for men, control of chlamydia infection globally is nearly impossible.  Application of this easy-to-use Chlamydia Rapid Test to detect chlamydia trachomatis antigen in the male patient is simple, quick, and convenient.  The Chlamydia Rapid Test is designed specifically for men and will allow doctors to diagnose the chlamydia infection quickly and successfully.  This Chlamydia rapid test is both accurate and swift, allowing men to be tested and treated on site in one visit.  It is hoped that the Chlamydia rapid test, or STD test, will also be of particular use in the developing world, where management of Chlamydia in men is often based on self-diagnosis and specific diagnostic tests are rarely available. The Chlamydia Rapid Test is an effective screening control and good for health clinics or doctor’s offices where the male patient can get tested and wait for results.  The Chlamydia Rapid Test contains easy-to-use components for convenient and effective treatment of male patients.

CHLAMYDIA RAPID TEST RESULTS

The Chlamydia Rapid Test Kit utilizes the chemical extraction of a carbohydrate antigen from chlamydia followed by the utilization of migratory color immunoassay technology for the qualitative detection of Chlamydia trachomatis. In the Chlamydia Rapid test procedure, a unique set of polyclonal and monoclonal antibodies are reemployed. On the Chlamydia Rapid Test, one antibody is immobilized on a porous membrane while the other antibody is conjugated to dye particles as signaling component. A swab specimen from a patient is treated with extraction reagent A and B to extract the antigen.  The Chlamydia rapid test dipstick is then immersed in the extraction sample. The liquid migrates through the absorbent area and along the membrane on the Chlamydia rapid test.  If Chlamydia trachomatis antigen is present on the Chlamydia rapid test, the labeled antibody-dye conjugate binds to it, forming an antibody-antigen complex. As the mixture flows along the membrane of the Chlamydia rapid test, the complex is captured by the antibody immobilized in the test zone (T) of the membrane, producing a visible rose-pink color band. Another dye-conjugated reagent on the Chlamydia rapid test is captured by the antibody immobilized in the control zone (C) of the membrane.  A rose-pink line in the Chlamydia rapid test zone ( T ) indicates the presence of Chlamydia trachomatis antigen. A rose-pink line in the control zone (C) indicates the Chlamydia rapid test is working properly. When only a control line appears with no test line, Chlamydia trachomatis antigen has not been detected and the Chlamydia rapid test result is considered negative. The control line on the Chlamydia rapid test gives an added measure of quality control by demonstrating antibody recognition, assuring that the Chlamydia rapid test procedure was performed correctly, and that the Chlamydia rapid test reagents are chemically active. A desiccant is enclosed with the Chlamydia rapid test device to stabilize the reactive agents.

Diagnostic Automatic/Cortez Diagnostics, Inc.’s Chlamydia Rapid Test Kit is one of the best STD test kits on the market today.  The Chlamydia Rapid Test is an effective and reliable tool to test and treat female and male patients who are susceptible to chlamydia infection.  We also offer other convenient and highly effective STD test kits:  HIV Rapid Tests, Gonorrhea Rapid Tests, Syphilis Rapid Tests, Chlamydia IgA ELISA Kit, Chlamydia IgG ELISA Kit, Chlamydia IgM ELISA Kit, HIV ELISA Kits, Syphilis ELISA Kits, and HSV ELISA Kits.  For more information on the Chlamydia Rapid Test Kit, or any other STD test kit, please contact our Customer Service Department.

ROTAVIRUS RAPID TEST

Medical tests conducted on the efficiency of the Rotavirus Rapid Test have shown that the Rotavirus Rapid Test is equally as accurate as the Rotavirus ELISA test available on the market today.  The test results revealed that the Rotavirus Rapid Test was just as sensitive as the direct electron microscopy of the Rotavirus ELISA test.   The Rapid Rotavirus Antigen Test has shown 98% sensitivity and 97% specificity compared to the Rotavirus ELISA test results.  Thus, the studies concluded that the Rotavirus Rapid Test is an accurate and rapid qualitative method for the detection of rotavirus in stools of symptomatic children.

Of course, Rotavirus ELISA kits are highly effective due to their reproductibility, easy interpretation, and their allowing simultaneous performance of several tests at one time.  For a number of years, Rotavirus ELISA Kits have been an important technique for the diagnosis of rotavirus infection.  Although particularly suited for testing large numbers of clinical specimens, Rotavirus ELISA tests often required several hours to complete, and their complexity limited their use to larger laboratories.  The ease of performance and time to completion clearly favored the Rotavirus Rapid Test.  The studies concluded that the Rotavirus Rapid test is particularly suited not only for major laboratories but also for physicians’ offices, clinics, and field work in rural or tropical settings.

Diagnostic Automation/Cortez Diagnostics, Inc. offers a one-step Rotavirus Rapid Test that is an in vitro qualitative immunocromatographic assay for the rapid detection of rotavirus antigens in human stool specimen.  The Rotavirus Rapid Test results are intended to aid in the diagnosis of rotavirus infection and to monitor the effectiveness of therapeutic treatment. This Rotavirus Rapid Test is for in vitro diagnostic use only.

To perform the Rotavirus rapid test, an aliquot of diluted stool sample is added to the sample well of the Rotavirus rapid test cassette.  The sample on the Rotavirus Rapid Test flows through a label pad containing rotavirus antibody coupled to red-colored colloidal gold.  If the sample on the Rotavirus rapid test contains rotavirus antigens, the antigen will bind to the antibody coated on the colloidal gold particles to form antigen-antibody-gold complexes. These complexes move on the nitrocellulose membrane by capillary action toward the Rotavirus rapid test line region on which rotavirus specific antibodies are immobilized.  As the complexes reach the Rotavirus rapid test line, they will bind to the antibody on the membrane in the form of a line. A second red control line will always appear in the Rotavirus rapid test result window to indicate that the Rotavirus rapid test has been correctly performed and the Rotavirus rapid test device functions properly.  If rotavirus antigen is not present or lower than the detection limit of the Rotavirus rapid test, only the control line will be visible.  If the control line does not develop, the Rotavirus rapid test is invalid.

Overall, with its proven high sensitivity and specificity, Diagnostic Automation/Cortez Diagnostics, Inc.’s OneStep Rotavirus Antigen RapiCardTM InstaTest is highly effective, inexpensive, and simple to use. Expected values for any given population should be determined for each laboratory. The positivity rate of any given laboratory may vary depending on geographic location, season, and living environment.  The Rotavirus Rapid Test is available in cassette format only.  Each Rotavirus rapid test cassette contains a test strip with rotavirus specific antibody on the Rotavirus rapid test region of the membrane and colored rotavirus antibody-gold conjugate pad.  For more information about this Rotavirus Rapid Test, or on our Rotavirus ELISA Kits, please contact our Customer Service Department.

NEWLY ARRIVED – DENGUE NS1 ELISA KIT

In addition to its Dengue ELISA Kit for lgG, lgM, and lgG/M antibody detection, Los Angeles based Diagnostic Automation/Cortez Diagnostics, Inc. is pleased to announce a newly arrived Dengue ELISA Kit – Dengue NS1 Antigen ELISA kit which is an Enzyme Linked Immunosorbent Assay for the detection of Dengue virus in human serum even prior to the presence of lgM or lgG antibodies.  Dengue NS1 ELISA Kit provides an excellent methodology for specifically detecting NS1 antigen in human serum.

DENGUE NS1 ELISA KIT  – PRODUCT FEATURES

The Dengue NS1 ELISA Kit is an excellent assay that contains a high level of sensitivity and specificity in detecting the NS1 antigen of Dengue virus.  The Dengue NS1 ELISA Kit is a rapid and reliable ELISA test that contains sufficient reagents for one plate of 96 wells (12 x 8 strips) each.  The user friendly Dengue NS1 ELISA Kit contains components that are convenient and easy to use.  The Dengue NS1 ELISA Kit has easy-to-read controls to determine positive or negative results.  Because of the complications associated with dengue infection, it would be beneficial to have a Dengue NS1 ELISA kit diagnosis early in the illness.  Consequently, the Dengue NS1 ELISA Kit is a useful tool for detecting dengue infection during the first few days of fever. 

The Dengue NS1 ELISA kit uses one enzymatically amplified, two-step sandwich-type immunoassay to detect low levels of NS1 in serum.  In this Dengue NS1 ELISA kit, controls and unknown serum samples are diluted in sample dilution buffer, containing secondary antibody, and incubated in microtitration wells.  These wells on the Dengue NS1 ELISA kit have been coated with a highly effective NS1 antibody and then blocked.  NS1 antigens present in the samples on this Dengue NS1 ELISA kit are then sandwiched between the capture and secondary antibodies.  The presence of NS1 antigen on this Dengue NS1 ELISA kit is confirmed by the colorimetric response obtained using an enzyme-conjugate-HRP and liquid TMB substrate.  Once the reaction is stopped on the Dengue NS1 ELISA kit, the enzymatic turnover of the substrate is determined by absorbance measurement at 450 nanometers.  The values obtained, on this Dengue NS1 ELISA kit, for the negative and positive sera serve as guidelines as to determining if a sample contains NS1 antigen.

DENGUE NS1 ELISA KIT – TEST RESULTS

Recent studies have confirmed the diagnostic accuracy of Dengue NS1 ELISA Kits for their overall sensitivity to detecting dengue antigens. The sensitivity and specificity of Dengue NS1 ELISA Kits were determined to be good, and the Dengue NS1 ELISA Kit was judged an effective tool for diagnosis of dengue infection, especially within the first four days of illness.  Early detection of dengue virus by a Dengue NS1 ELISA test can help in early confirmation and management of this virus.  The Dengue NS1 ELISA Kit has the ability to improve the diagnostic algorithm contributing significantly to the clinical treatment and control of dengue viral infections.  This Dengue NS1 ELISA Kit would be applicable for both dengue diagnosis and epidemiological studies. Collectively, various studies indicate that tests like this Dengue NS1 ELISA kit deserve inclusion in the diagnostic approach to detection of dengue virus in patients.

The Dengue ELISA Kits are available in two formats:  Dengue ELISA Kit for detection of lgG, lgM and lgG/lM antibodies, and Dengue NS1 ELISA Kit for detection of NS1 antigens in human serum.  For more information on either the Dengue ELISA Kit or Dengue NS1 ELISA Kit, please contact Customer Service.

Dengue Antigen NS1 Elisa kit

Click Here To See Dengue NS1 ELISA kit Product Page: 

http://rapidtest.com/index.php?i=Dengue-NS1-ELISA-kit—Antigen&id=682&cat=17

NEW PRODUCT – DENGUE NS1 RAPID TEST

Los Angeles based Diagnostic Automation/Cortez Diagnostics, Inc. has been a leader in the development of infectious disease rapid tests for more than 20 years.  Our One-Step Dengue NS1 RapiDip Insta Test that identifies the dengue virus, follows the tradition of quality and reliability expected by our customers around the world.  This Dengue NS1 Rapid Test is a chromatographic immunoassay for the qualitative detection of non-structural protein 1 (NS1) antigens in whole blood, serum, or plasma.  The Dengue NS1 Rapid Test serves as an aid in the screening and diagnosis of early Dengue infections.  The Dengue NS1 rapid test will aid in the rapid diagnosis of Dengue virus in human serum even prior to the presence of IgM or IgG antibodies.

DENGUE NS1 RAPID TEST -  NOTABLE FEATURES

The Dengue NS1 Rapid Test is based on lateral flow technique.  The convenient and easy-to-use Dengue NS1 Rapid Test contains 25 test strips in a user-friendly pack size, and 64 individual sample reservoir wells designed for easy specimen collection.  The main advantage to the Dengue NS1 Rapid Test is how fast the results can be obtained. The entire procedure of Dengue NS1 Rapid Test takes approximately 30 minutes.

Timely, sensitive, and specific diagnosis of dengue virus is important for early detection of dengue virus infection.  However, some available tools for dengue diagnosis are time-consuming.  The use of tests like the Dengue NS1 Rapid Test as a first-line test for the screening of dengue infected patients, using serum samples collected during the onset of clinical symptoms, could help to accelerate the diagnosis of dengue fever in clinical diagnostic laboratories.    Rapid and easy diagnosis of dengue using Dengue NS1 Rapid Test can assist patient triage and care management.  For example, during an epidemic outbreak, the ability to triage those patients suspected of dengue fever and to quickly establish an anti-viral therapy with use of the Dengue NS1 Rapid Test, might improve the rates of disease control drastically.  Recent studies have shown that sensitivity and specificity tests, like the Dengue NS1 rapid test, were highly specific to DENV NS1, and the Dengue NS1 rapid test produced enhanced diagnoses at high detection rates.  Thus, the Dengue NS1 Rapid Test presents the ideal method of testing as it is rapid, easily applicable, sensitive, and highly specific.

DENGUE NS1 RAPID TEST – FAST RESULTS

Dengue virus, a virus belonging to the Flavavirus group of viruses, is one of the most significant mosquito-borne diseases in the world in terms of morbidity and mortality. Transmitted principally by the mosquito types Aedes aegypti and Aedes albopictus, the virus is found commonly throughout the tropic and subtropic regions of the world. Symptoms of dengue fever include high fever, headache, muscle pain and skin rash. The complications often associated with this infection are dengue hemorrhagic fever or dengue shock syndrome.

The detection of DENV NS1 using the Dengue NS1 Rapid Test offers a fast route to a dengue diagnosis.  Physicians using this Dengue NS1 Rapid Test in early convalescence diagnostic strategy on patients should be able to obtain rapid and specific dengue diagnosis within a few minutes.  The positive correlation between viral load, disease progression and detection of NS1, suggests that tests like the Dengue NS1 Rapid Test might be a valuable test to include in dengue triage protocols in areas of high incidence of dengue infection.

The Dengue NS1 Rapid Test is a qualitative, membrane based immunoassay for the detection of NS1 antigen in human serum.  The Dengue NS1 Rapid Test membrane is pre-coated with NS1 specific antibody on the Dengue NS1 Rapid test line region and utilizes a separate control to assure assay flow and performance.  If NS1 antigen is present on the Dengue NS1 Rapid Test, a red line will appear at the test line.  The red line at the control region should always appear if the Dengue NS1 Rapid Test is performed correctly.  The presence of this red line on the Dengue NS1 Rapid Test verifies that proper flow has occurred and catastrophic failure of the conjugate has not occurred.  The Dengue NS1 Rapid Test is positive for the NS1 antigen when the control line (C) and the test line (T) appear in the Dengue NS1 Rapid Test area. A faint line on the Dengue NS1 Rapid Test is considered a positive result. The Dengue NS1 Rapid Test is negative when just the control line appears.

RELATED PRODUCTS

The Dengue Rapid Tests are available in two formats:  Dengue NS1 Rapid Test for detection of NS1 antigens in human serum, and Dengue Rapid Test for testing lgG, and lgM antibodies.  Also available are the Dengue NS1 ELISA Kit for detection of NS1 antigens in human serum, and Dengue ELISA Kit for detection of lgG, lgM, and lgG/lgM antibodies.  For more information on either the Dengue ELISA Kit, Dengue NS1 ELISA Kit, Dengue NS1 Rapid Test, or Dengue Rapid Test, please contact our Customer Service.

Dengue NS1 Rapid test

CLICK HERE TO SEE DENGUE NS1 RAPID TEST PRODUCT PAGE:

http://www.rapidtest.com/index.php?i=Infectious-Disease-&-other-tests&id=683&cat=26