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Hangzhou AllTest Biotech CO.,LTD 

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My oldest daughter actually has Lyme disease. She spent almost 1 year in a wheelchair because of Lyme. She is doing very well now. I used 2 of the samples. 1 to test my Lyme diagnosed daughter and 1 to test my daughter who does not have Lyme. Your tests worked well. My daughter with Lyme tested positive and the one who does not tested negative.

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Medical Diagnosis PSA Qualitative Rapid Test Kits For Prostate Cancer Risk

Product Details:

Place of Origin:China
Brand Name:AllTest
Certification:CE0123, ISO13485
Model Number:TPS-Q402

Payment & Shipping Terms:

Minimum Order Quantity:N/A
Price:negotiation
Packaging Details:25 Tests/kit box, 50 kit box/Carton
Delivery Time:2-4 Weeks
Payment Terms:Ex works
Supply Ability:10 M tests/month
Detailed Product Description
Format: Strip/ Cassette Specimens: Whole Blood, Serum,plasma
Accuracy: 98.6% Certificate: CE,ISO 13485
Storage: 2-30℃ Shelf Time: 24months
Cut-off: 4 Ng/ml

One Step Prostate Specific Antigen (PSA)  Qualitative Test Kit for the diagnosis of Prostate Cancer Risk

 

Applications:

 

The PSA Qualitative Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for qualitative detection of Prostate Specific Antigen in whole blood, serum or plasma.
 

Description:

 

Prostate cancer is the one of the most common types of cancer found in man. The incidence of prostate cancer increases with age and accounts for a growing number of  newly diagnosed patients. Prostate specific antigen (PSA) is produced primarily in the prostate gland and is secreted into the prostate ducts and at ejaculation serves to liquefy the seminal coagulum. Virtually all healthy males under 50 years of age have PSA concentration under 4.0 ng/ml. If PSA level is above 20 ng/ml, the patient most likely to have prostate cancer. Some studies indicated that elevated total PSA levels are found in serum from patients who have prostate cancer cells metastasized throughout their bodies. Other studies indicated that Free PSA, which can not foam a complex with serine protease tends to be more abundant in patients with benign prostatic hyperplasia. Rapid PSA test use antibodies which can equally recognize both free PSA and PSA-ACT complex

 

How to use?

 

Allow the test, specimen, buffer and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it as soon as possible.
2. Place the cassette on a clean and level surface.
For Serum ,Plasma or Venipuncture Whole Blood specimens:
· Hold the dropper vertically and transfer 1 drop of serum or plasma (approximately 40ul) or 2 drops of venipuncture whole blood (approximately 80 ul) to the specimen well (S) of test cassette, then add 1 drop of buffer (approximately 40 ul) and start the timer. See illustration below.
For Fingerstick Whole Blood specimen:
· To use a capillary tube: Fill the capillary tube and transfer approximately 80 ul of fingerstick whole blood specimen to the specimen well (S) of test cassette, then add 1 drop of buffer (approximately 40 ul) and start the timer. See illustration below.
· To use hanging drops: Allow 2 hanging drops of fingerstick whole blood specimen (approximately 80 ul) to fall into the specimen well (S) of test cassette, then add 1 drop of buffer (approximately 40 ul) and start the timer. See illustration below.


3. Wait for the colored line(s) to appear*. Read results at 5 minutes. Do not interpret the result after 10 minutes.


*Note: if migration is not observed in the result window after 30 seconds, add one or two extra drops of buffer.


 Note: It is suggested not to use the buffer, beyond 6 months after opening the vial.

 

Medical Diagnosis PSA Qualitative Rapid Test Kits For Prostate Cancer Risk

 

 

INTERPRETATION OF RESULTS
 
(Please refer to the illustration above)
 
POSITIVE:* Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the test region (T).
 
*NOTE: The intensity of the color in the test line region (T) will vary depending on the concentration of PSA present in the specimen. Therefore, any shade of color in the test region (T) should be considered positive.
 
NEGATIVE: One colored line appears in the control region (C). No apparent colored line appears in the test 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 cassette. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

 

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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