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Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection

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We are satisfied with your quality & services so far. The HIV 1/2 antibody Test performance is perfect.

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Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection

China Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection supplier
Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection supplier Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection supplier

Large Image :  Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection

Product Details:

Place of Origin: China
Brand Name: New Life
Certification: ISO13485,CE
Model Number: Cassette

Payment & Shipping Terms:

Minimum Order Quantity: 5000pcs
Price: USD0.5-USD2
Packaging Details: 1pc/pouch, 25pcs/box
Delivery Time: 20-30days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 2000000pcs/month
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Detailed Product Description
Category: Tumor Mark Format: Cassette/STRIP
Specimen: WB/Serum/Plasma Testing Time: 5-15 Minutes
Shelf Life: 24 Months Application: Alpha-protein
Accuracy: 99.22%

High Accuracy Tumor Marker AFP Rapid cassette, for detecting Alpha-protein in serum, gold colloidal method

 

 

Intended Use:

 

The AFP Rapid Test Cassette (Whole Blood /Serum /Plasma) is a rapid chromatographic immunoassay for the qualitative detection of AFP in whole blood, serum or plasma to aid in the diagnosis of Hepatocellular Carcinoma or fetal open neural tube defects.

 

Test Principle:

 

The AFP Rapid Test Cassette (Whole Blood /Serum /Plasma) is a qualitative membrane based immunoassay for the detection of AFP in whole blood, serum or plasma. The membrane is pre-coated with anti-AFP antibodies on the test line region. During testing, the specimen reacts with the particle coated with anti-AFP antibodies. The mixture migrates upward on the membrane chromatographically by capillary action to react with anti-AFP antibodies on the membrane and generate a colored line. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear in the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.

 

 

TEST PROCEDURE

 

 

1. Bring the pouched test device to room temperature(15-30℃) prior to testing. Do not open the pouch until ready

to begin testing.

2. Remove the device from the sealed pouch and lay it on a flat and dry surface.

3. Using the provided pipette, add one drop of fresh specimen to the sample well.

4. Hold the buffer bottle vertically and add 1 drop to the sample well. /If using a pipette, change a new one to avoid

cross-contamination. Draw and transfer 2-3 drops of buffer to the sample well.

5. Read the result between 15-20minutes. Do not read results after 20 minutes.

 

 

INTERPRETATION OF RESULTS

 

 

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 TP antibodies 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.

 

 

Alpha Protein Cancer Test Kit Serum Specimen Gold Colloidal Qualitative Detection

 

 

PERFORMANCE CHARACTERS:

 

Sensitivity and Specificity

 

The AFP Rapid Test Cassette (Whole Blood /Serum /Plasma) has correctly identified a panel of specimens and has been compared to a leading commercial AFP EIA test using clinical specimens. The results show that the relative sensitivity of the AFP Rapid Test Cassette (Whole Blood /Serum /Plasma) is 99.4%, and the relative specificity is 99.0%.

 

 

Method EIA Total Results
AFP Rapid Test Cassette Results Positive Negative
Positive 317 5 322
Negative 2 503 505
Total Results 319 508 827

 

Relative Sensitivity: 99.4% (95%CI*: 97.8%-99.9%) * Confidence Interval

 

Relative Specificity: 99.0% (95%CI*: 97.7%-99.7%)

 

Accuracy: 99.2% (95%CI*: 98.3%-99.7%)

 

 
ORIENT NEW LIFE MEDICAL CO., LTD.
Contact: Jerry Meng
Email: Jerry @ newlifebiotest .com
Tel. +86 18657312116
SKYPE enetjerry

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Contact Person: Jerry Meng

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