Información del producto
ELISA Kit for Inhibin Beta A (INHbA)
Información adicional
Stabillity at RT
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
Applications
Enzyme-linked immunosorbent assay for Antigen Detection.
Detection Range
39.06-10,000pg/mL
Sensitivity
The minimum detectable dose of this kit is typically less than 14.33pg/mL
Specificity
No significant cross-reactivity or interference between Inhibin Beta A (INHbA) and analogues was observed.
This assay has high sensitivity and excellent specificity for detection of Inhibin Beta A (INHbA).
Research Area
Endocrinology
Hormone metabolism
Reproductive science
Tumor immunity
Hormone metabolism
Reproductive science
Tumor immunity
Organism species
Rattus norvegicus (Rat)
Item Name
Inhibin Beta A
Assay Length
2h
Method
Competitive Inhibition
Sample Type
serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Procedure
1. Prepare all reagents, samples and standards
2. Add 50µ
3. Aspirate and wash 3 times
4. Add 100µ
5. Aspirate and wash 5 times
6. Add 90µ
7. Add 50µ
And then add 50µ
C
C
C
L Stop Solution. Read at 450 nm immediately.
L Substrate Solution. Incubate 10-20 minutes at 37°
L prepared Detection Reagent A immediately.
L prepared Detection Reagent B. Incubate 30 minutes at 37°
L standard or sample to each well.
Shake and mix. Incubate 1 hour at 37°
1. Prepare all reagents, samples and standards
2. Add 50µ
3. Aspirate and wash 3 times
4. Add 100µ
5. Aspirate and wash 5 times
6. Add 90µ
7. Add 50µ
And then add 50µ
C
C
C
L Stop Solution. Read at 450 nm immediately.
L Substrate Solution. Incubate 10-20 minutes at 37°
L prepared Detection Reagent A immediately.
L prepared Detection Reagent B. Incubate 30 minutes at 37°
L standard or sample to each well.
Shake and mix. Incubate 1 hour at 37°
Test Principle
This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to INHbA has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled INHbA and unlabeled INHbA (Standards or s
Precision
CV(%) = SD/meanX100
Inter-Assay: CV<12%
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Inhibin Beta A (INHbA) were tested on 3 different plates, 8 replicates in each plate.
Intra-Assay: CV<10%
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Inhibin Beta A (INHbA) were tested 20 times on one plate, respectively.
UniProt ID
P18331