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China 15 minutes FABP Fluorescence Immunoassay Test Cassette 10T 25T
China 15 minutes FABP Fluorescence Immunoassay Test Cassette 10T 25T

  1. China 15 minutes FABP Fluorescence Immunoassay Test Cassette 10T 25T

15 minutes FABP Fluorescence Immunoassay Test Cassette 10T 25T

  1. MOQ: N/A
  2. Price: Negotiation
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Supply Ability 10 M tests/month
Delivery Time 2-4 Weeks
Packaging Details 10T/25T
Product Diagnostic FABP Test Use By Citest GO fluorescence Immunoassay Analyzer In Human whole blood /serum /plasma
Cat. No. FI-HFA-402
Principle Fluorescence Immunoassay
Format Cassette
Specimen WB/S/P
Certificate CE
Reading Time 15 minutes
Pack 10T/25T
Storage Temperature 4-30℃
Shelf Life 2 Years
Linearity range 1-120ng/ml , R≥0.990
Cut-Off 8ng/mL
Accuracy The test deviation is≤±15%
Analytical sensitivity as low as 1ng/ml in whole blood, serum or plasma
Brand Name Citest
Model Number FI-HFA-402
Certification CE
Place of Origin -

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  1. Product Details
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Product Specification

Supply Ability 10 M tests/month Delivery Time 2-4 Weeks
Packaging Details 10T/25T Product Diagnostic FABP Test Use By Citest GO fluorescence Immunoassay Analyzer In Human whole blood /serum /plasma
Cat. No. FI-HFA-402 Principle Fluorescence Immunoassay
Format Cassette Specimen WB/S/P
Certificate CE Reading Time 15 minutes
Pack 10T/25T Storage Temperature 4-30℃
Shelf Life 2 Years Linearity range 1-120ng/ml , R≥0.990
Cut-Off 8ng/mL Accuracy The test deviation is≤±15%
Analytical sensitivity as low as 1ng/ml in whole blood, serum or plasma Brand Name Citest
Model Number FI-HFA-402 Certification CE
Place of Origin -
High Light FABP Fluorescence Immunoassay Test CassetteFluorescence Immunoassay Test Cassette 10TFluorescence Immunoassay FABP Test 25T

【PERFORMANCE CHARACTERISTICS】

1. Accuracy

The test deviation is ≤±15%.

2. Sensitivity

The H-FABP Test Cassette can detect levels of H-FABP as low as 1ng/ml in whole blood, serum or plasma.

3. Detection range

1-120ng/ml

4. Linearity range

1-120ng/ml , R≥0.990

5. Precision

C.V. ≤15%

 

 

 

Fast Result (15 minutes)

Simple Operation (Less Training Required)

Objective (Results Read by Analyzer)

Stringent Quality Control Insure High Accuracy

User-friendly (Simple Plug & Play Operation)

High Efficiency (Both STAT Testing and Batch Testing)

Diagnostic FABP Test Use By Citest GO fluorescence Immunoassay Analyzer In Human whole blood /serum /plasma

 

A test for measuring FABP in whole blood /serum /plasma with the use of Citest TM Go fluorescence Immunoassay Analyzer. For professional in vitro diagnostic use only.

 

Application And Description:

 

FABP is a newly introduced plasma marker of acute myocardial infarction (AMI). The plasma kinetics of FABP (15kD) closely resemble those of H-FABP in that elevated plasma concentrations are found within 2 hours after AMI and return to normal generally within 18 to 24 hours. But the concentration of FABP in the skeletal muscle is 20 times lower than in cardiac tissue (for H-FABP the same content for cardiac and skeletal tissue), that makes FABP to be more cardiac specific than H-FABP. This makes FABP a useful biochemical marker for the early assessment or exclusion of AMI.

 

FABP also appears to be a useful plasma marker for the estimation of myocardial infarct size. FABP is suitable for use as a standard in immunoassay for early detection of acute myocardial infarction, immunogen for antisera production, mass FABP standard, FABP biochemical and immunochemical studies, tracer for iodination.

 

Principle Fluorescence Immunoassay
Format Cassette
Specimen WB/S/P
Certificate CE
Reading Time 15 minutes
Pack 10T/25T
Storage Temperature 4-30℃
Shelf Life 2 Years
Cut-Off 8ng/mL

 

How to use?

 

Refer to Citest TM Go Fluorescence Immunoassay Analyzer Operation Manual for the complete instructions on use of the Test. The test should be conducted in room temperature.

 

Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.

 

1. Turn on the Analyzer power. Then according to the need, select “standard test” or “Quick test” mode.

2. Take out the ID card and insert it into the Analyzer port.

3. Serum/Plasma: Pipette 50μL serum/plasma into the buffer tube, mix the specimen and the buffer well.

4. Whole blood: Transfer 75μL whole blood into the buffer tube with pipette; mix the specimen and the buffer well.

5. Add diluted specimen with a Pipette: Pipette 85μL diluted specimen into the sample well of the test cassette. Start the timer at the same time.

6. There are two test modes for Citest TM Go Fluorescence Immunoassay Analyzer, Standard Test mode and Quick Test mode.

 

Please refer to the user manual of Citest TM Go Fluorescence Immunoassay Analyzer for details.

 

“Quick test” mode: After 15 minutes of adding sample,Insert the test cassette into the Analyzer, click “QUICK TEST”, fill the test information and click "NEW TEST" immediately. The Analyzer will automatically give the test result after a few seconds.

“Standard test” mode: Insert the test cassette into the Analyzer immediately after adding specimen, click “STANDARD TEST”, fill the test information and click "NEW TEST" at the same time, The Analyzer will automatically countdown 15 minutes. After the countdown, the Analyzer will give the result at once.

 

The H-FABP Test Cassette is based on Fluorescence Immunoassay to measure H-FABP in whole blood or plasma as an aid in the diagnosis of acute myocardial infarction (AMI).The test result is calculated by Fluorescence Immunoassay Analyzer.

 

Catalogue Number Item Name Sample Test Range KIT size
FI-HFA-402 H-FABP Test Cassette WB/S/P 1-120 ng/mL 10T/25

 

Company Details

Bronze Gleitlager

,

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 and 

Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer,Exporter,Trading Company

  • Total Annual:

    80000000-100000000

  • Employee Number:

    500~10000

  • Ecer Certification:

    Verified Supplier

CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ... CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ...

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  • CITEST DIAGNOSTICS INC.
  • 170-422, Richards Street, Vancouver BC V6B 2Z4, CANADA
  • https://www.citesttestkit.com/

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