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

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

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

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Supply Ability	10 M tests/month
Delivery Time	2-4 Weeks
Packaging Details	10 T
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
Brand Name	Citest
Model Number	CCR-401/CCR-402/CCR-U401/CCR-T402/CCR-U402
Certification	CE
Place of Origin	-

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Product Specification


Supply Ability	10 M tests/month	Delivery Time	2-4 Weeks
Packaging Details	10 T	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	Brand Name	Citest
Model Number	CCR-401/CCR-402/CCR-U401/CCR-T402/CCR-U402	Certification	CE
Place of Origin	-
High Light	Cardiac Marker CrP Diagnostic test ，C Reactive Protein 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.

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.

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.

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Business Type:

Manufacturer,Exporter,Trading Company 
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Total Annual:

80000000-100000000
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Employee Number:

500~10000 
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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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