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HIV 1/2 ELISA kit

HIV 1/2  ELISA kit
HIV 1/2  ELISA kit
HIV 1/2  ELISA kit
HIV 1/2  ELISA kit

HIV 1/2 ELISA kit Specification

  • Control Type
  • Manual, using microplate reader
  • Shape
  • Rectangular packaging
  • Accuracy
  • >99% sensitivity, >99% specificity
  • Temperature Resistance
  • Store at 2C 8C
  • Features
  • Ready to use reagents, High sensitivity and specificity, Easy usage protocol, CE/ISO certified
  • Type
  • Diagnostic ELISA Kit
  • Dimension (L*W*H)
  • Box packaging, approx. 20cm x 15cm x 5cm
  • Equipment Type
  • ELISA kit
  • Equipment Materials
  • Plastic, Paper, Silica Gel
  • Material
  • Biological/chemical reagents, microplate strips
  • Application
  • Detection of HIV 1/2 antibodies in serum/plasma
 

HIV 1/2 ELISA kit Trade Information

  • Minimum Order Quantity
  • 50 Kits
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID)
  • Supply Ability
  • 50000 Kits Per Week
  • Delivery Time
  • 7 Days
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
 

About HIV 1/2 ELISA kit



The HIV 1/2 ELISA Kit is a best-seller among laboratory professionals, offering unprecedented value through its affordable pricing and optimum performance. This paragon diagnostic ELISA kit includes 96 tests per pack and boasts a shelf life of 18 months. Harnessing the reliable enzyme-linked immunosorbent assay (ELISA) at a 450 nm wavelength, this kit utilizes indirect assay format and requires minimal sample volume (50-100 L). Approved by CE, ISO 13485, and WHO, it guarantees >99% sensitivity and specificity, with ready-to-use reagents and positive/negative controls included. The rectangular, durable packaging ensures safe storage between 2C and 8C.

Material Features, Application & Commercial Uses

Constructed with high-grade plastic, paper, silica gel, and biological/chemical reagents, the HIV 1/2 ELISA Kit achieves remarkable performance in detecting HIV 1/2 antibodies in serum or plasma. Its precise application supports clinical laboratories, diagnostic centers, and commercial testing facilities, ensuring dependable results and streamlined workflow. The kit's advanced design and comprehensive accessories facilitate commercial use in routine screening, epidemiological surveys, and quality assurance programs, enhancing healthcare efficacy and safety.


FOB Port, Delivery & Packaging Details

Orders for the HIV 1/2 ELISA Kit can be handed over at major Indian FOB ports. Delivery time is prompt, typically aligning with the proposal amount and expenditure agreed upon in procurement contracts. Each kit comes securely packed in sturdy rectangular boxes (20cm x 15cm x 5cm) with barcode labeling for efficient tracking and expiry date indication. The packaging ensures all accessories and reagents are intact, safeguarding sample integrity and quality throughout transit and delivery.


FAQ's of HIV 1/2 ELISA kit:


Q: How does the HIV 1/2 ELISA kit ensure high accuracy in antibody detection?

A: The kit follows an indirect ELISA format with enzyme-linked detection, achieving more than 99% sensitivity and specificity. It includes both positive and negative controls, ensuring reliable and reproducible results for HIV 1/2 antibody screening.

Q: What materials and accessories are included in each kit?

A: Every kit contains microplate strips, ready-to-use reagents, positive and negative controls, silica gel, an instruction manual, and sturdy plastic and paper packaging to maintain product integrity and usability.

Q: When can laboratory professionals use the HIV 1/2 ELISA kit after delivery?

A: The kit is ready for use immediately upon receipt, provided it is stored at the recommended temperature of 2C to 8C. All reagents and accessories are pre-packed and labeled for instant setup.

Q: Where is the HIV 1/2 ELISA kit typically applied in commercial or clinical settings?

A: This kit is ideal for use in hospital laboratories, blood banks, diagnostic centers, and research institutions where precise serological HIV detection is crucial for patient screening and disease management.

Q: What is the process for using the HIV 1/2 ELISA kit?

A: Laboratory professionals add serum/plasma samples (50-100 L), incubate for approximately 2 hours, and read results at a 450 nm wavelength using a microplate reader, following the manual control protocol included.

Q: What benefits does the kit offer in terms of standards and compliance?

A: The HIV 1/2 ELISA kit complies with international regulatory standards, including CE, ISO 13485, and WHO prequalification, ensuring product quality, traceability, and reliability in diverse operational environments.

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