Japanese Encephalitis IgG ELISA

Japanese Encephalitis IgG ELISA Specification

Control Type
Manual Process

Shape
Rectangular wells

Features
Ready-to-use components, Reliable Results, Shelf life at least 12 months, Controls included

Accuracy
High sensitivity and specificity

Temperature Resistance
2C - 8C (Storage)

Type
Diagnostic ELISA Kit

Equipment Type
ELISA test kit

Equipment Materials
Plastic wells, Reagents, Microtiter plate

Material
Plastic, Chemical Reagents, Enzyme Conjugate

Application
Detection of IgG antibodies to Japanese Encephalitis Virus in human serum or plasma

Japanese Encephalitis IgG ELISA 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 Japanese Encephalitis IgG ELISA

Experience the superlative performance of our Japanese Encephalitis IgG ELISA diagnostic kit, now available at a Special Rate for limited reservations. Celebrated by laboratories worldwide, this kit offers perfect accuracy, thanks to high sensitivity, specificity, and ready-to-use components. Each kit reserves 96 tests, utilizing an indirect ELISA principle for qualitative and semi-quantitative detection of IgG antibodies to Japanese Encephalitis Virus in human serum or plasma. The fresh, reliable results can be obtained within a compact 60-90 minute total assay time. With WHO-standard calibration, included controls, and industry-leading shelf life of 12-18 months, this ELISA test kit is the discerning choice for any clinical setting. Exported by a celebrated manufacturer and supplier in India, reserve yours today.

Superior Features and Application Areas of Japanese Encephalitis IgG ELISA

The Japanese Encephalitis IgG ELISA kit stands out for its high-accuracy, reliability, and fresh, ready-to-use materials. Suitable for clinical diagnostic laboratories, research institutions, and hospitals, its unique strengths include rapid incubation time, calibrated controls, and WHO reference standardization. This celebrated kit provides superlative diagnostic confidence in detecting IgG antibodies for Japanese Encephalitis, making it the perfect selection for precise epidemiological investigations and routine screenings.

Packaging, Sample Policy, and Main Export Markets for Japanese Encephalitis IgG ELISA

Carefully dispatched in secure packaging, every kit is drop-off ready to ensure integrity from supplier to laboratory. Valuation policies prioritize both quality and affordability, providing sample support upon inquiry for qualified clients. With robust international logistics, our main export markets include Asia, Europe, Africa, and the Middle East. Trust in prompt delivery and global distribution from our celebrated Indian manufacturing facility for all your ELISA kit needs.

FAQ's of Japanese Encephalitis IgG ELISA:

Q: How does the Japanese Encephalitis IgG ELISA kit work?

A: The kit uses an indirect ELISA process to detect IgG antibodies specific to the Japanese Encephalitis Virus in human serum or plasma samples. The results are interpreted using color intensity and comparison with included positive and negative controls.

Q: What is the total assay time for the Japanese Encephalitis IgG ELISA kit?

A: The entire assay process can be completed within 60-90 minutes, offering quick turnaround of fresh, reliable results.

Q: Where can this ELISA kit be used effectively?

A: This kit is suitable for diagnostic laboratories, hospitals, and research facilities seeking to detect or screen for IgG antibodies to Japanese Encephalitis Virus.

Q: When should the Japanese Encephalitis IgG ELISA kit be stored during transport and usage?

A: The kit should be stored and transported at a stable temperature between 2C and 8C to maintain freshness and efficacy, with a shelf life of 12-18 months.

Q: What are the major benefits of using this ELISA kit?

A: It provides high sensitivity and specificity, reliable results, easy manual control, and includes all necessary controls and reagents calibrated to WHO reference standards.