Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
- Product No.MEA830Mu
- Organism SpeciesMus musculus (Mouse) Same name, Different species.
- Test MethodCompetitive Inhibition
- Assay Length3h
- Detection Range2.47-200ng/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 0.88ng/mL.
- Sample TypeSerum, plasma and other biological fluids
- Download Instruction Manual
- UOM 48T96T 96T*5 96T*10 96T*100
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Packages (Simulation)
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Packages (Simulation)
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Results demonstration
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Typical Standard Curve
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ISO9001: 2008, ISO13485: 2003 Registered
Specificity of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
This assay has high sensitivity and excellent specificity for detection of Mini Samples Follicle Stimulating Hormone (FSH).
No significant cross-reactivity or interference between Mini Samples Follicle Stimulating Hormone (FSH) and analogues was observed.
Recovery of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
Matrices listed below were spiked with certain level of recombinant Mini Samples Follicle Stimulating Hormone (FSH) and the recovery rates were calculated by comparing the measured value to the expected amount of Mini Samples Follicle Stimulating Hormone (FSH) in samples.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 90-104 | 96 |
| EDTA plasma(n=5) | 78-104 | 101 |
| heparin plasma(n=5) | 89-96 | 93 |
Precision of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Follicle Stimulating Hormone (FSH) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Follicle Stimulating Hormone (FSH) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Linearity of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mini Samples Follicle Stimulating Hormone (FSH) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
| Sample | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 80-91% | 87-105% | 84-102% | 82-97% |
| EDTA plasma(n=5) | 92-99% | 96-104% | 95-104% | 97-104% |
| heparin plasma(n=5) | 81-105% | 82-93% | 81-95% | 81-95% |
Stability of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Assay procedure summary of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
1. Prepare all reagents, samples and standards;
2. Add 25µL standard or sample to each well.
And then add 25μL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 50µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 50µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 25µL Stop Solution. Read at 450 nm immediately.
Test principle of the Mini Samples ELISA Kit for Follicle Stimulating Hormone (FSH)
This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to FSH has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled FSH and unlabeled FSH (Standards or samples) with the pre-coated antibody specific to FSH. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of FSH in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of FSH in the sample.
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