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STANDARD F Chikungunya IgM/IgG FIA test kit

145 INR/Kit

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Product Details:

Function Detection of IgM and IgG antibodies to Chikungunya virus
Measurement Range Qualitative Detection (Positive/Negative)
Display Type Requires compatible FIA Analyzer Display
Accuracy > 97%
Usage Type Laboratory & Clinical Diagnostics
Storage Instructions Store at 2C to 30C, keep away from direct sunlight
Instruments Type Immunoassay Test Kit
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STANDARD F Chikungunya IgM/IgG FIA test kit Price And Quantity

Price 145 INR/Kit
Minimum Order Quantity 2 Box

Sensitivity IgM: 98.0%, IgG: 97.6% (as per manufacturer)
Lot Number Information Provided on packaging
Test Time About 15 minutes per specimen
Kit Contents Test devices, sample pipettes, buffer solution, instruction manual
Sample Type Human serum or plasma
Number of Tests per Kit 20
Compatible Analyzer STANDARD F Analyzer (SD Biosensor)
Test Principle Antibody-antigen reaction detected by FIA
Intended Use For professional use in laboratory diagnosis

STANDARD F Chikungunya IgM/IgG FIA test kit Product Specifications

Condition New
Real-Time Operation Yes
Color White & Blue (Kit), Vials: Transparent
Display Type Requires compatible FIA Analyzer Display
Noise Level Silent Operation
Voltage Depends on Analyzer Specification
Power Consumption Depends on Analyzer
Function Detection of IgM and IgG antibodies to Chikungunya virus
Technology Fluorescent Immunoassay (FIA)
Measurement Range Qualitative Detection (Positive/Negative)
Use Detection of Chikungunya IgM/IgG Antibodies
Shelf Life 18 months from manufacturing date
Operating Type Automatic via Analyzer
Equipment Type In Vitro Diagnostic Test Kit
Weight Approx. 500 grams (Kit box)
Features High Sensitivity and Specificity, Rapid Results
Dimension (L*W*H) Kit Box: Approx. 200 x 150 x 70 mm
Portable Yes
Instruments Type Immunoassay Test Kit
Storage Instructions Store at 2C to 30C, keep away from direct sunlight
Wall Mounted No
Accuracy > 97%
Power Source Analyzer (External Power Required)
Usage Type Laboratory & Clinical Diagnostics
Material Plastic, Paper, Reagent Chemicals

Sensitivity IgM: 98.0%, IgG: 97.6% (as per manufacturer)
Lot Number Information Provided on packaging
Test Time About 15 minutes per specimen
Kit Contents Test devices, sample pipettes, buffer solution, instruction manual
Sample Type Human serum or plasma
Number of Tests per Kit 20
Compatible Analyzer STANDARD F Analyzer (SD Biosensor)
Test Principle Antibody-antigen reaction detected by FIA
Intended Use For professional use in laboratory diagnosis

STANDARD F Chikungunya IgM/IgG FIA test kit Trade Information

Payment Terms Cash Advance (CA), Cash in Advance (CID), Cheque, Telegraphic Transfer (T/T)
Main Export Market(s) Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
Main Domestic Market All India

Product Description

STANDARD F Chikungunya IgM/IgG FIA qualitatively analyzes Chikungunya virus specific IgM and IgG antibodies in serum, plasma and whole blood using fluorescent immunoassay. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.

Advantage

Able to perform qualitative analysis with high sensitivity and specificity by using fluorescent substance
Objective result - Eliminates the subjectivity of a visual result
Automatic strip recognition by reading the information stored in 2D barcode

Specification
- Specimenï
  Whole blood, Serum, Plasma
- Test timeï
  15 mins
- Specimen volumeï
  10 l
- Sensitivityï
  97.2% (35/36)
- Specificityï
  98.9% (178/180)

Technical Details

Reliable Chikungunya Detection

This rapid FIA test kit ensures prompt identification of Chikungunya infection through strong accuracy and sensitivity. By detecting IgM and IgG antibodies, healthcare professionals can distinguish between current and past infections, facilitating well-informed clinical decisions for patient care. Its 15-minute operational time is particularly valuable in settings requiring swift diagnosis.

Efficient Workflow and User-Friendly Design

Each kit is designed for ease of use, providing all essential components including sample pipettes and buffers, pre-measured for accuracy. Instructions are included to ensure correct processes are followed. The kit supports efficient workflows within clinical and laboratory environments, thanks to its simple setup and automatic processing through the STANDARD F Analyzer.

Storage and Portability Convenience

The kit is compact (approx. 200 x 150 x 70 mm, 500 grams), portable, and stable for up to 18 months when maintained at 2C to 30C, away from direct sunlight. This allows for flexible storage and handling in diverse laboratory and clinical setups across India, ensuring availability when needed.

FAQ's of STANDARD F Chikungunya IgM/IgG FIA test kit:

Q: How is the STANDARD F Chikungunya IgM/IgG FIA test performed?

A: To perform the test, collect a serum or plasma sample from the patient, add the sample and buffer to the test device, and insert it into the STANDARD F Analyzer. The analyzer will automatically process the reaction and provide results within approximately 15 minutes.

Q: What types of samples can be used with this test kit?

A: The test kit is compatible with human serum or plasma samples. Whole blood and other body fluids are not recommended for this particular assay.

Q: When should this kit be used for Chikungunya diagnosis?

A: This kit is intended for professional laboratory or clinical settings where rapid detection of Chikungunya IgM and IgG antibodies is needed. It is used to support diagnosis during acute or convalescent phases based on antibody response.

Q: Where can I use the STANDARD F Chikungunya IgM/IgG FIA test kit?

A: The kit is designed for use in hospitals, diagnostic laboratories, and clinical research settings. It is not intended for home or self-testing, and must be operated by trained professionals.

Q: What is the process of reading test results with this kit?

A: After the sample and buffer are loaded into the test device, insert the device into the STANDARD F Analyzer. The analyzer interprets the fluorescence signals and displays a qualitative result (positive or negative) on its screen.

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

A: The main benefits include rapid turnaround (about 15 minutes), high sensitivity and specificity, ease of use, and compatibility with fully automated analyzer systems for consistent, reliable results.

Q: How should the test kit be stored and what is its shelf life?

A: Store the kit at 2C to 30C and keep it away from direct sunlight. The test kit remains stable and effective for up to 18 months from the manufacturing date, as marked on the packaging.

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