MERIL HIV ELISA TEST KIT

MERIL HIV ELISA TEST KIT Specification

Shelf Life
12-24 months

Accuracy
>99%

Measurement Range
Qualitative (Reactive/Non-reactive)

Function
Detects antibodies to HIV-1 and HIV-2

Instruments Type
ELISA Test Kit

Storage Instructions
Store at 2C-8C; Do not freeze

Usage Type
Diagnostic laboratory use

Features
High sensitivity, high specificity, ready-to-use reagents

Equipment Type
HIV ELISA Test Kit

Material
Plastic, Microtiter Plate

Condition
New

Technology
Enzyme Linked Immunosorbent Assay (ELISA)

Portable
Yes

Wall Mounted
No

Real-Time Operation
No

Operating Type
Manual

Use
Detection of HIV-1 and HIV-2 antibodies in human serum or plasma

Dimension (L*W*H)
Standard kit size

Weight
Approx. 250-500 g per kit

Color
White/Blue (as per kit design)

About MERIL HIV ELISA TEST KIT

Shop Now for the MERIL HIV ELISA TEST KIT, a superior diagnostic solution designed for professional laboratories. Personalise your testing workflow with this grandiose kit, containing a 96-well microtiter plate, ready-to-use reagents, sample diluent, conjugate, substrate, controls, and detailed instructions. Get enviable accuracy exceeding 99% sensitivity and specificity for reliable HIV-1 and HIV-2 antibody detection via ELISA technology. CE marked and IVD certified, this portable kit ensures qualitative, colorimetric results within 1.5 to 2 hours. Intended for serum/plasma, this kit assures robust performance and elevated diagnostic confidence. Secure your batch for superior laboratory outcomes!

Application and Usage of MERIL HIV ELISA TEST KIT

The MERIL HIV ELISA TEST KIT is intended exclusively for professional diagnostic laboratory use and is used as a reliable tool to detect HIV-1 and HIV-2 antibodies in human serum or plasma. Its core application is in clinical settings for screening and confirmation. This equipment type is essential in plant or hospital laboratories, ensuring stringent quality and superior results for large-scale or batch testing, contributing to public health and patient care initiatives.

Sample Policy, Certifications, and Payment Terms

Each MERIL HIV ELISA TEST KIT shipment is CE marked and IVD certified, ensuring adherence to global regulations. Kits are dispatched with a batch or lot number and include comprehensive documentation. Sample policy allows for secure quotations before purchasing, while products are shipped promptly upon confirmation of payment terms. Bulk orders from suppliers, traders, and wholesalers in India benefit from streamlined payment processes. Kits are carefully packaged and shipped with temperature considerations to maximize shelf life and performance.

FAQ's of MERIL HIV ELISA TEST KIT:

Q: How does the MERIL HIV ELISA TEST KIT detect HIV antibodies?

A: The kit utilizes enzyme-linked immunosorbent assay (ELISA) technology to detect antibodies specific to HIV-1 and HIV-2 in human serum or plasma through a colorimetric reaction, interpreted visually or via spectrophotometer.

Q: What are the contents included in the MERIL HIV ELISA TEST KIT?

A: Each kit includes a 96-well microtiter plate, sample diluent, conjugate, substrate, stop solution, positive and negative controls, and a detailed instruction leaflet, with all reagents ready-to-use.

Q: When should the MERIL HIV ELISA TEST KIT be used?

A: This kit is intended for professional diagnostic laboratory use and should be used when accurate and rapid screening or confirmation of HIV infection is required in clinical or hospital settings.

Q: Where should the kit be stored for optimal performance?

A: The kit should be stored at 2C-8C at all times and never frozen, ensuring all reagents maintain their high sensitivity, specificity, and accuracy throughout their 12-24 months shelf life.

Q: What are the main benefits of using this kit?

A: The principal benefits include high sensitivity and specificity (>99%), fast incubation time (about 1.5 to 2 hours), qualitative results, and reliable detection of both HIV-1 and HIV-2 antibodies.

Q: How is the testing process conducted?

A: Simply add patient serum or plasma into the wells, follow with reagents as per the instruction leaflet, incubate as directed, then interpret the color development to determine reactive or non-reactive status.