Send Message
CITEST DIAGNOSTICS INC. info@citestdiagnostics.com
C Reactive Protein CrP Diagnostic Test 97.8% Accurate Cardiac Marker Rapid Test Kits

C Reactive Protein CrP Diagnostic Test 97.8% Accurate Cardiac Marker Rapid Test Kits

  • High Light

    Cardiac Marker CrP Diagnostic test

    ,

    C Reactive Protein Test 97.8% Accurate

    ,

    Cardiac Marker Rapid Test Kits

  • Product
    C-reactive Protein (CrP) Diagnostic Rapid Test Cassette , Accuate Cardiac Marker Rapid Test Kits
  • Cat No.
    CCR-401/CCR-402/CCR-U401/CCR-T402/CCR-U402
  • Principle
    Chromatographic Immunoassay
  • Format
    Cassette
  • Specimen
    WB/S/P
  • Certificate
    CE
  • Reading Time
    5 Minutes
  • Pack
    10 T
  • Storage Temperature
    2-30°C
  • Shelf Life
    2 Years
  • Sensitivity
    >99.9
  • Specificity
    97.5%
  • Accuracy
    97.8%
  • Cut-Off
    10 μg/mL*, 0.5 μg/mL,10-40-80 μg/mL, 10-30 μg/mL
  • Place of Origin
    -
  • Brand Name
    Citest
  • Certification
    CE
  • Model Number
    CCR-401/CCR-402/CCR-U401/CCR-T402/CCR-U402
  • Minimum Order Quantity
    N/A
  • Price
    negotiation
  • Packaging Details
    10 T
  • Delivery Time
    2-4 Weeks
  • Supply Ability
    10 M tests/month

C Reactive Protein CrP Diagnostic Test 97.8% Accurate Cardiac Marker Rapid Test Kits

C-reactive Protein (CrP) Diagnostic Rapid Test Cassette , Accuate Cardiac Marker Rapid Test Kits

 

A rapid test for the diagnosis of inflammatory condition by detecting C-reactive protein qualitatively in whole blood, serum or plasma CE certified

 

 

Applications:

 

The CRP Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of human CRP in whole blood, serum or plasma as an aid in the diagnosis of inflammatory condition. The cut-off of the test is 10 μg/ml.

 

 

Description:

 

C-reactive Protein (CrP) in patient’s sera has been found in association with acute infections, necrotic conditions and a variety of inflammatory disorders. There is a strong correlation between serum levels of CrP and the onset of the inflammatory process. Monitoring the levels of CrP in patient’s sera indicates the effectiveness of treatment and the assessment of patient recovery. It is used in particular to differentiate bacterial infections from virus infections.

 

 

How to use?

 

Bring tests, specimens, buffer, and/or controls to room temperature (15-30°C) before use.
1. Remove the Test Cassette from its sealed pouch, and place it on a clean, level surface. For best results, the assay should be performed within one hour.
2. Open the tube with the diluted sample .Transfer 3 drops of (approx. 120ul) mixed specimens to sample well. Start the timer.
3. Wait for the colored lines to appear. The result should be read at 5 minutes. Do not interpret the results at 10 minutes.

 

 

 

C Reactive Protein CrP Diagnostic Test 97.8% Accurate Cardiac Marker Rapid Test Kits 0

C Reactive Protein CrP Diagnostic Test 97.8% Accurate Cardiac Marker Rapid Test Kits 1


 

For  CCR-401 :

 

The CRP Rapid Test Dipstick (Whole Blood/Serum/Plasma) is a rapid chromatographic  immunoassay for the qualitative detection of human CRP in whole blood, serum or plasma  as an aid in the diagnosis of inflammatory condition. The cutoff of the test is 10 μg/ml.
 
SUMMARY 
 
C-reactive Protein (CRP) in patient’s sera has been found in association with acute  infections, necrotic conditions and a variety of inflammatory disorders.1 There is a strong  correlation between serum levels of CRP and the onset of the inflammatory process.Monitoring the levels of CRP in patient’s sera indicates the effectiveness of treatment and  the assessment of patient recovery.3 It is used in particular to differentiate bacterial  infections from virus infections.
 
PRINCIPLE
 
The CRP Rapid Test Dipstick (Whole Blood/Serum/Plasma) detects C-reactive Protein  through visual interpretation of color development on the internal dipstick. The sample  now moves through the test dipstick from bottom to top. If the test sample contains CRP, it  attaches to the CRP antibody which is conjugated with a red gold colloidal for color  marking. The more CRP is contained in the sample, the more red lines become visible.
 
A red line should always appear in the control (C) line area. It serves as a procedural  control, confirming that sufficient specimen volume was used and indicates an adequate  membrane wicking and proper procedural technique. 
 

 

DIRECTIONS FOR USE
 
Bring tests, specimens, buffer, and/or controls to room temperature (15-30°C)  before use.
 
1. Remove the Test Dipstick from its sealed pouch, and place it on a clean, level surface.
For best results, the assay should be performed within one hour.
 
2. Open the tube with the diluted sample and put the test dipstick with the arrow pointing  end into the liquid. Make sure to dip the test not beyond the line for the maximum  immersion depth (Max line). Avoid in any case a direct wetting of the result area by  spilling or dipping the test beyond MAX line.
 
3. Leave the test for minimum 10 seconds in the diluted sample until the slightly  pink-colored liquid front becomes visible in the result area.
 
4. Take out the test dipstick and place it on a plain and non-absorbent surface.  Alternatively, the test dipstick can remain in the tube. Start the timer as the test starts  to run.
 
5. As the test begins to run you will observe a colored liquid migrate along the membrane  of the reaction area. Interpret results at 5 minutes. Please stick exactly to this time line  to ensure correct semi-quantitative results. 
C Reactive Protein CrP Diagnostic Test 97.8% Accurate Cardiac Marker Rapid Test Kits 2
 
INTERPRETATION OF RESULTS
 
(Please refer to the illustration above)
POSITIVE:* Two lines appear. One colored line should be in the control line region (C)  and another apparent colored line should be in the test line region (T).
 
*NOTE: The intensity of the color in the test line region (T) will vary depending on the  concentration of CRP antigen present in the specimen. Therefore, any shade of color in  the test line region (T) should be considered positive.
 
NEGATIVE: One colored line appears in the control line region (C). No line appears in  the test line region (T).
 
INVALID: Control line fails to appear. Insufficient specimen volume or incorrect  procedural techniques are the most likely reasons for control line failure. Review the  procedure and repeat the test with a new test. If the problem persists, discontinue using  the test kit immediately and contact your local distributor.