Dengue Combo Test Kit: Rapid HIV Ab & P24 Ag detection system

Short Description:

Human Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to HIV 1 and/or HIV 2 and P24 antigen in whole blood, serum or plasma.


Product Detail

Product Tags

Discover a groundbreaking innovation in the field of disease detection with QL biotech’s innovative Dengue Combo Test Kit - Rapid HIV Ab & P24 Ag detection system. This state-of-the-art kit is a go-to tool for the quick, qualitative detection of antibodies related to HIV 1&2 and P24 antigen. The Dengue Combo Test Kit readily works on whole blood, serum or plasma samples, making it a versatile option for a wide array of laboratory settings. This rapid test kit employs a membrane-based immunoassay technology that ensures accurate and quick results. With detection capability for both HIV antibodies and P24 antigen, our Dengue Combo Test Kit plays a pivotal role in diagnosing and managing HIV in patients. QL biotech has dedicated its resources to creating high-quality, reliable medical diagnostics tools, and the Dengue Combo Test Kit stands as a testament to our dedication to quality and innovation. The kit not only enables accurate detection, but it also ensures results are provided swiftly, facilitating faster decision-making and treatment considerations. Test kits such as the Dengue Combo are instrumental in today’s medical field, where accuracy and speed are of the essence. With this in mind, QL biotech has designed the Dengue Combo Test Kit to meet and exceed the diagnostic needs of healthcare facilities globally.

PRINCIPLE

Human Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative, membrane based immunoassay for the detection of antibodies to HIV 1&2 and P24 antigen in whole blood, serum or plasma. The membrane is precoated with recombinant HIV antigens to HIV 1&2 antibody and P24 antibody to HIV P24 antigen. During testing, the whole blood, serum or plasma specimen reacts with HIV antigen or P24 antibody coated particles in the test strip. The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with recombinant HIV antigen or P24 antibody on the membrane in the test line regions. If the specimen contains antibodies to HIV 1 and/or HIV 2 and/or P24 antigen, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain HIV 1 and/or HIV 2 antibodies and/or P24 antigen, no colored line will appear in the test line region indicating a negative result. To serve as a procedural control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.


MATERIALS

Materials Provided
● Test devices ● Disposable specimen droppers
● Buffer ● Package insert
Materials Required But Not Provided
● Specimen collection containers ● Lancets (for fingerstick whole blood only)
● Centrifuge (for plasma only) ● Timer
● Disposable heparinized capillary tubes and dispensing bulb (for fingerstick whole blood only)

 

DIRECTIONS FOR USE

    • ● Test devices 
      ● Disposable specimen droppers 
      ● Buffer 
      ● Package insert 
      Materials Required But Not Provided 
      ● Specimen collection containers 
      ● Lancets (for fingerstick whole blood only) 
      ● Centrifuge (for plasma only) 
      ● Timer 
      ● Disposable heparinized capillary tubes and dispensing bulb (for fingerstick whole blood only)


    PERFORMANCE CHARACTERISTICS

    Sensitivity

    Human Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (Whole

    Blood/Serum/Plasma) has been tested by anti-HIV 1 low titer performance panel, anti-HIV 2 performance panel and anti-HIV 1 seroconversion panel (Boston Biomedica, Inc.). And it has also been compared with leading commercial EIA HIV test on clinical specimens. The results show that

    HIV 1&2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) is very sensitive to HIV 1 and/or HIV 2 antibodies.

    Specificity

    The specificity of the test is comparable to a leading commercial HIV EIA test. Human Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (Whole Blood/Serum/Plasma) is highly specific for anti-HIV 1 and/or HIV 2 compared to a leading commercial HIV EIA test.

    Relative Sensitivity: 99.9% (99.3%-100.0%)*Relative Specificity: 99.6% (99.1%-99.9%)*

    Relative Accuracy: 99.8% (99.4%-99.9%)* * 95% Confidence Interval

    Precision

    Intra Assay

    Within-run precision has been determined by using 15 replicates of three specimens: a negative, a low positive and a high positive. The negative, low positive and high positive values were correctly identified 99.5% of the time.

    Inter-Assay

    Between-run precision has been determined by 15 independent assays on the same three specimens: a negative, a low positive and a high positive. Three different lots of Human

    Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (Whole Blood/Serum/Plasma) have been tested using negative, low positive and high positive specimens. The specimens were correctly identified 99.5% of the time.

     



    This kit is more than just a rapid test device. It’s a crucial tool for disease control, patient care, and medical advancement. Invest in the Dengue Combo Test Kit - your solution for accurate, swift, and reliable HIV detection. Please note that the Dengue Combo Test Kit is designed for laboratory use and should be used by trained personnel to ensure accurate results. Always consult a healthcare professional for interpretation of test results.

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