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Progesterone Prog Rapid Quantitative Test Fluorescence Immunoassay

Progesterone Prog Rapid Quantitative Test Fluorescence Immunoassay

Progesterone Rapid Quantitative Test kit

Prog Rapid Quantitative Test kit

High Sensitive progesterone test kit

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Product Details
Response Time:
High Sensitive,rapid Test
Room Temperature
12 Months
Application In:
WWHS NIR-1000 Dry Fluoroimmunoassay Analyser
Payment & Shipping Terms
Minimum Order Quantity
Packaging Details
Paper Box
Delivery Time
Two weeks
Supply Ability
5000 Kits per Week
Product Description

Progesterone(Prog)Rapid Quantitative Test (Fluorescence Immunoassay)

.Why to choose us?

1. Limits of detection

No higher than 1.40 ng/mL.

2. Accuracy

The relative deviation from the target value is within ±15%.

3. Precision

The within and between assay coefficient of variations are within 15%.

4. Linear range

Within the linear range (1.40~ 60.00 ng/mL), the linear correlation coefficient R≥0.990.


Ⅱ.Components of product




Test cards


It is composed of fluorescent pad (coated with fluorescent labeled Prog monoclonal antibody and fluorescent labeled biotin), nitrocellulose membrane (coated with Prog-BSA and GSA), absorbent paper and backing.

Sample diluent


Phosphate buffer

ID card


With specific stand curve file


Ⅲ.Intended use of a product

   Progesterone(Prog)Rapid Quantitative Test kit is used for quantitative determination of progesterone in human whole blood, plasma and serum.

   Therefore, the detection of progesterone can be used to determine ovulation and luteal phase defects. In addition, the detection of progesterone can also monitor progesterone treatment and evaluate early pregnancy.


Ⅳ.Test procedure

1. Before the test, please read the instructions completely. If the test card about Progesterone(Prog)Rapid Quantitative Test kit  and sample are stored in cold storage, they should be balanced at room temperature (15-30)℃ for not less than 30min before use.

2. Start NIR-1000 dry fluoroimmunoassay analyser and correctly select the corresponding sample type on the instrument.

3. Take out the ID card, make sure that the batch number of the ID card is consistent with that of the test card, and insert the ID card into the ID card port of the instrument.

4. Take out the test card from the aluminum foil bag and use it within 15 minutes.

5. Place the test card on a clean horizontal table and mark it horizontally.

6. Mix 100 µL of sample with 200µL of sample diluent. Apply 100 µL of diluted samples to the well of the test card.

7. At 15 minutes after addition of samples, insert the test card into NIR-1000 dry fluoroimmunoassay analyser and click the “Instant test” button to read the results.


Ⅴ.Reference interval


Gender Phase

2.5th percentile


97.5th percentile


Male / 0 1.5
Female Follicular phase 0 1.9
Ovulatory phase 0 12.0
Luteal phase 1.7 28.7
Menopause 0 1.4
Pregnancy(<12weeks) 11.0 53.0
Pregnancy(12-24weeks) 21.5 60.0

It is strongly recommended that each laboratory should determine its own normal and abnormal values based on population.



Progesterone Prog Rapid Quantitative Test Fluorescence Immunoassay 0

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