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Intend Use
Premature rupture of membranes(PROM) is one ofthe most difficult problems faced by obstetrics and gynecology, with an incidence of about 10%, which causes many complications before and after deliveryTherefore, timely and accurate diagnosis of premature rupture of membranes is the key to appropriate treatment.This test kit adopts the principle of immunochromatographic assay, could detect the insulin-like growth factor binding protein-1(lGFBP-1) in human amniotic fuid to provide important reference for the diagnosis of premature rupture of fetal membranes.
| Description | Specimen | Format | Package | Registraction |
| IGFBP-1(PROM)Test | Secretion | Cassette | 1T | CE |
| IGFBP-1(PROM)Test | Secretion | Strip | 20T | CE |
Features
1.High Specifcity to Amniotic Fluid
2.High sensitivity
3.Easy use, good performance
Test Procedure
1.Adopt the cotton swab in the package, extend the vagina and take specimens, or slowly insert into the vaginal5-7cm, gently rotate theswab for 30 seconds,and take the secretions as soon as possible
2. Then insert the swab specimen into the buffer tube with rotary dilution and fullimmersion.lf cassette format, please tighten the cap othe buffer tube)
3.Remove the test from the foil pouch at room temperature. The detection should be completed in one hour after the tests taken out offoil pouch
4. lf it is the cassette, place it on a clean, dry and fat table, use the dropper to absorb and drop 3 drops of bufer into the test on the desk;ifit is the strip, insert it into the buffer, not over the max line, take out the test strip when the purplish red material can be seen on the strip,place the test strip on the table.
5.Interpret the result in 15 minutes.
Storage
The kit should be stored in the dark environment at4~ 30 C ,the validity is 24 months since the date of production. Within one month after the period of validity, the product performance shall meet the requirements of 3-4.
| Clothing | |
| FDA | Certified |
| CE | Certified |