Comparison

CLIA Kit for Inhibin Alpha (INHa)

Item no. CCA395Mu-24T
Manufacturer Cloud-Clone
Amount 24T
Category
Type Clia
Specific against Mouse
ECLASS 5.1 27150207
ECLASS 6.1 27150207
ECLASS 8.0 27150207
ECLASS 9.0 27150207
ECLASS 10.0.1 32161000
ECLASS 10.1 32161000
ECLASS 11.0 32161000
UNSPSC 41116126
Alias INH-A
Available
Quantity options
Detection range
12.35-1, 000pg/mL
Organism species
Mus musculus (Mouse)
Sensitivity
The minimum detectable dose of this kit is typically less than 5.11pg/mL
Sample type
Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay length
2h
Method
Competitive Inhibition
Specificity

This assay has high sensitivity and excellent specificity for detection of Inhibin Alpha (INHa).
No significant cross-reactivity or interference between Inhibin Alpha (INHa) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Inhibin Alpha (INHa) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Inhibin Alpha (INHa) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Stability

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
1. Prepare all reagents, samples and standards;
2. Add 50µ L standard or sample to each well.
        And then add 50µ L prepared Detection Reagent A immediately.
        Shake and mix. Incubate 1 hour at 37° C;
3. Aspirate and wash 3 times;
4. Add 100µ L prepared Detection Reagent B. Incubate 30 minutes at 37° C;
5. Aspirate and wash 5 times;
6. Add 100µ L Substrate Solution. Incubate 10 minutes at 37° C;
7. Read RLU value immediately.
Test principle
The microplate provided in this kit has been pre-coated with a monoclonal antibody specific to Inhibin Alpha (INHa). A competitive inhibition reaction is launched between biotin labeled Inhibin Alpha (INHa) and unlabeled Inhibin Alpha (INHa) (Standards or samples) with the pre-coated antibody specific to Inhibin Alpha (INHa). 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 Inhibin Alpha (INHa) in the sample. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is reverse proportional to the Inhibin Alpha (INHa) level in the sample or standard.
Research Area
Endocrinology; Reproductive science; Hormone metabolism;

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 24T
Available: In stock
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