About JMITRA HIV Elisa Test Kit
- Use of Envelope Antigens gp41, C terminus of gp120 for HIV-1 and gp36 for HIV-2 & simultaneously detection of p24 antigen with p24 monoclonal antibodies
- Detection of Group O & subtype C for HIV-1 prevalent in India
- Colour coded reagents to monitor the procedural steps
- Assay procedure: 120 mins
- Shelf life: 15 months at 2-8C
- Sensitivity 100% & Specificity 99.97%
- Significant reduction in window period
- Easy to use on automated and semi-automatic processor
High Accuracy and ReliabilityJMITRA's HIV Elisa Test Kit is meticulously engineered to provide more than 99% sensitivity and specificity, significantly reducing the likelihood of false positive or false negative results. Each batch is validated according to national and international standards to ensure consistent performance in clinical environments.
User-Friendly Design With Ready-to-Use ReagentsThis kit comes with all necessary reagents pre-measured and ready for use, eliminating the need for complex preparations. The simple manual procedure, supported by positive and negative controls, streamlines HIV antibody detection and enhances result confidence for users.
Comprehensive Application RangeSuitable for hospitals, blood banks, and diagnostic laboratories, the JMITRA HIV Elisa Test Kit is compatible with most ELISA plate readers. Its versatile assay format and portable design make it ideal for various diagnostic settings requiring quick, accurate results.
FAQ's of JMITRA HIV Elisa Test Kit:
Q: How does the JMITRA HIV Elisa Test Kit detect HIV antibodies?
A: This test kit uses the Indirect ELISA method to identify antibodies against HIV-1 and HIV-2 in human serum or plasma. The patient sample is added to a microplate well where HIV antigens are coated, allowing specific antibodies in the sample to bind, followed by detection through enzyme-linked indicators.
Q: What sample volume is needed and what controls are provided?
A: Each test requires 100 L of human serum or plasma. The kit includes both positive and negative controls, ensuring every testing run can be validated for accuracy and reliability.
Q: When should this kit be used and by whom?
A: The kit is intended for use in hospitals, blood banks, and diagnostic laboratories by trained professionals for screening and diagnostic purposes, helping to identify individuals with exposure to HIV infection.
Q: Where can I interpret the test results-manually or with equipment?
A: Results can be interpreted visually or via an Optical Density (OD) ELISA plate reader, making the process flexible according to laboratory capabilities.
Q: What are the benefits of using this assay format and technology?
A: It offers outstanding accuracy (>99%), rapid results, minimal sample volume, and ease of use, backed by ready-to-use reagents. These features make it an excellent choice for efficient routine diagnostics.
Q: How should the kit be stored and what is its shelf life?
A: Store the kit at 2-8C and protect it from light to maintain reagent integrity. The shelf life is 12-18 months from the date of manufacture, supporting reliable long-term storage.
Q: Is the kit compatible with standard laboratory equipment?
A: Yes, the microplate format is compatible with most ELISA plate readers, making integration into existing laboratory workflows straightforward.