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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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Stable Rapid Allergen Test Kits Insulin Like Growth Factor Binding Protein

Product Details:

Place of Origin:CHINA
Brand Name:AllTest
Certification:CE
Model Number:CASSETTE

Payment & Shipping Terms:

Minimum Order Quantity:500
Packaging Details:25 tests per kit
Supply Ability:100 Million a year
Detailed Product Description
Format: Cassette Specimen: Vaginal Discharge
Kit Size: 25T/Kit Color: Blue
Storage: 2-30°C Shelf Time: 24months

 

iGFBP-1 Rapid Test Cassette CE certified

 

 

Applications: 

 

The Insulin-like growth factor-binding protein 1 (iGFBP-1) rapid test (vaginal secretion) is a visually interpreted, qualitative immunochromatographic test device for detection of iGFBP-1 in vaginal secretions during pregnancy, which is a major protein marker of the amniotic fluid in a vaginal sample. The test is intended for professional use to help diagnose the rupture of fetal membranes (ROM) in pregnant women.

 

Description: 

 

Insulin-like growth factor-binding protein 1 (IBP-1) known as placental protein 12 (PP12) is a protein that in humans is encoded by the IGFBP1 gene. IGF-binding proteins (IGFBPs) is believed to be important in the regulation of fetal and neonatal growth. We previously reported that the profiles of IGFBPs in fetal cord serum (FCS) were dependent on the growth/metabolic status of the fetus. It can be detected in cervical secretions of pregnant women with preterm uterine contractions, and whether their presence predicts an increased risk of preterm delivery. The abundance of insulin-like growth factor binding protein-1 at the maternal-fetal interface in severely preeclamptic pregnancies suggests that the binding protein may participate in the pathogenesis of the shallow placental invasion observed in this disorder. Low circulating insulin-like growth factor-I and elevated insulin-like growth factor binding protein-1 levels may contribute to restricted placental and therefore fetal growth.

 

 

How to use? 

 

Bring tests, specimens, buffer and/or controls to room temperature (15-30°C) before
use.

 

1. Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour.
2. Insert the swab into the dilute tube, rotate for 20 times. Then press the swab against the side of the tube and squeeze the bottom of the tube as the swab is withdrawn. Discard the swab.
3. Fit the cap of the tube. Remove the top part of the cap. Place the test device on a clean and level surface. Add 3 full drops of solution (approx. 100 μL) to the specimen well (S) and then start the timer.
4. Wait for the colored band to appear. The result should be read at 5 minutes. Do not interpret the result after 20 minutes.

Stable Rapid Allergen Test Kits Insulin Like Growth Factor Binding Protein

 

 
   

INTERPRETATION OF RESULTS

 

POSITIVE:
* A colored band appears in the control band region (C) and another colored band appears in the T band region.


NEGATIVE:
One colored band appears in the control band region (C). No band appears in the test band region (T).
 

INVALID:
Control band fails to appear. Results from any test which has not produced a control band at the specified reading time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.


NOTE:
1. The intensity of the color in test region (T) may vary depending on the concentration of aimed substances present in the specimen. Therefore, any shade of color in the test region should be considered positive. Besides, the substances level can not be determined by this qualitative test.
2. Insufficient specimen volume, incorrect operation procedure, or performing expired tests are the most likely reasons for control band failure.

 

 

QUALITY CONTROL

• Internal procedural controls are included in the test. A colored band appearing in the control region (C) is considered an internal positive procedural control. It confirms sufficient specimen volume and correct procedural technique.
• External controls are not supplied with this kit. It is recommended that positive and negative controls be tested as a good laboratory practice to confirm the test procedure and to verify proper test performance.

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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