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Progesterone Detection Kit (Fluorescence Dry Quantitative Immunoassay) Download the picture album

【 Characteristics 】

Method: Fluorescence dry quantitative immunoassay Assay measuring range: 0.37ng/mL ~40.00ng/mL Incubation time: 10 minutes Sample: Human serum, plasma (EDTA-K2 anticoagulant)50ul, whole blood (EDTA-K2 anticoagulant)80ul Reference range: Gender Stage reference range female Follicular phase <0.37-1.98ng/mL (5%CI-95%CI) Luteal phase <0.88-30.43ng/mL (5%CI-95%CI) Post-menopausal <0.37-0.8ng/mL (5%CI-95%CI) Early stage pregnancy <4.7->40ng/mL (10%CI-90%CI) Storage and Stability:  Detection Buffer is stable for 12 months at 2°C~8°C.  Sealed Test Device is stable for 12 months at 4°C~30°C.

Clinical application

Clinical Applications

l  Ovulation monitoring

Blood progesterone levels >5ng/ml suggest ovulation.

l  Evaluation of luteal function

Evaluation of luteal function: A lower than physiological blood progesterone level during the luteal phase is indicative of luteal insufficiency.

l   Ancillary diagnosis of ectopic pregnancy

In ectopic pregnancy, blood progesterone levels is very low, most patients < 15ng/ml.

l  Others

Aids in the diagnosis of pre-eclampsia, observation of placental function, prognostic assessment of in vitro fertilisation-embryo transfer, etc.

 


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