iGFBP-1 Rapid Test Device/Strip (Vaginal secretion)

Short Description:

The Insulin‐like growth factor‐binding protein 1 (iGFBP‐1) rapid test (vaginal secretion) is a visually interpreted, qualitative immunochromatographic dipstick test 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.


Product Detail

Product Tags

Product Parameters

Product Name

iGFBP-1 Rapid Test Device

iGFBP-1 Rapid Test Strip

Used for

For professional in vitro diagnostic use only.

Specimen

Vaginal secretion

Packing

20 tests/box , 1 test/polybag

MOQ

1000 tests

Diverse Coopetation Modes

OEM/ODM

 

STORAGE AND STABILITY

● The kit should be stored at 2‐30°C until the expiry date printed on the sealed pouch.
● The test must remain in the sealed pouch until use.
● Do not freeze.
● Cares should be taken to protect components in this kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipments, containers or reagents can lead to false results.

INTERPRETATION OF RESULTS


POSITIVE RESULT: 
*A colored band appears in the control band region (C) and another colored band appears in the T band region.
NEGATIVE RESULT:
One colored band appears in the control band region (C). No band appears in the test band region (T).
INVALID RESULT:
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.
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.

 


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