Scrub Typhus IgM ELISA kit

Scrub Typhus IgM ELISA kit Specification

Shape
Kit box

Display Type
Readout at 450 nm (Microplate Reader, not included)

Control Type
Positive and Negative controls included

Features
Ready to use, high accuracy, rapid results, user-friendly protocol

Temperature Resistance
Reagents stable at 2-8C

Accuracy
High Sensitivity and Specificity (>98%)

Type
Diagnostic Kit

Dimension (L*W*H)
225 x 150 x 65 mm (approx. kit box size)

Equipment Type
ELISA Test Kit

Equipment Materials
Kit box with reagents, microtiter plate strips, wash buffer, conjugate, substrate, stop solution, controls

Power
Not required (manual processing)

Material
Plastic (microtiter strips), reagents in sealed vials

Application
Qualitative detection of IgM antibodies to Orientia tsutsugamushi

Scrub Typhus IgM 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
6 Days

Main Export Market(s)
Australia, Asia, Central America, North America, Eastern Europe, South America, Africa, Middle East

About Scrub Typhus IgM ELISA kit

Unlock the power of eminent diagnostics with the Scrub Typhus IgM ELISA Kit-featured as a hot-selling and rarefied solution for serological detection of Orientia tsutsugamushi. This noteworthy kit enables qualitative screening and confirmation of Scrub Typhus infection, utilizing the proven Enzyme-linked Immunosorbent Assay (ELISA) principle. Delivering high accuracy (sensitivity and specificity >98%), it accommodates human serum or plasma samples with rapid results in ~90 minutes. Each kit includes essential controls, ready-to-use reagents, and microtiter strips, ensuring user-friendly operation and reliable outcomes for both clinical and research settings. Storage and transport are recommended at 2-8C.

Usage, Applications, and Features

The Scrub Typhus IgM ELISA Kit is designed for qualitative detection of IgM antibodies, supporting screening and confirmation of Scrub Typhus infection in hospitals, laboratories, and research centers. With its rapid assay time of approximately 90 minutes, the kit features a user-friendly protocol and ready-to-use reagents. High sensitivity and specificity plus the inclusion of positive and negative controls ensure accuracy and reliability-making it a trusted choice among diagnostic professionals across various application areas.

Packing, Delivery, and Sample Availability

Packing & dispatch of the Scrub Typhus IgM ELISA kit is handled with utmost care, using sturdy kit boxes and cold chain maintenance to preserve reagent quality during goods transport. Customers may request a sample, subject to applicable charges. Each kit is securely packaged for transit, ensuring safe arrival at your location. Delivery times depend on order volume and destination, but prompt shipment is always prioritized to meet urgent diagnostic needs efficiently.

FAQ's of Scrub Typhus IgM ELISA kit:

Q: How is the Scrub Typhus IgM ELISA kit used for detection?

A: The kit employs enzyme-linked immunosorbent assay (ELISA) for qualitative detection of IgM antibodies to Orientia tsutsugamushi in human serum or plasma samples. Results are interpreted via optical density measured at 450 nm.

Q: What equipment is required to process the test?

A: No powered equipment is needed for manual processing, but a microplate reader is necessary to measure optical density (OD) at 450 nm for result interpretation.

Q: When should the kit components be stored and transported?

A: All reagents should be stored and transported between 2-8C. Cold chain transport is strongly recommended to maintain reagent efficacy and integrity.

Q: Where can the kit be effectively applied?

A: This diagnostic kit is suitable for use in hospitals, clinical laboratories, research institutions, and public health centers for both screening and confirmation of Scrub Typhus infection.

Q: What are the benefits of using the featured kit controls?

A: Inclusion of positive, negative, and cut-off controls ensures accurate, reliable, and consistent interpretation of results, safeguarding against false positives or negatives.