ELISA Kit for Cholinergic Receptor, Muscarinic 2 (CHRM2)

Manufacturer Cloud-Clone
Type Elisa-Kit
Specific against Mouse
Amount 24T
Item no. SEB213Mu-24T
eClass 6.1 32160605
eClass 9.0 32160605
Alias CHR-M2; HM2; M-AChRM2; Muscarinic Acetylcholine Receptor M2; Cholinergic Receptor,Muscarinic 2
Quantity options
Detection range
Organism species
Mus musculus (Mouse)
The minimum detectable dose of this kit is typically less than 0.054ng/mL
Sample type
Tissue homogenates, cell lysates and other biological fluids.
Assay length
Double-antibody Sandwich

This assay has high sensitivity and excellent specificity for detection of Cholinergic Receptor, Muscarinic 2 (CHRM2).
No significant cross-reactivity or interference between Cholinergic Receptor, Muscarinic 2 (CHRM2) and analogues was observed.


Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Cholinergic Receptor, Muscarinic 2 (CHRM2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Cholinergic Receptor, Muscarinic 2 (CHRM2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%


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 100µ L standard or sample to each well. Incubate 2 hours at 37° C;
3. Aspirate and add 100µ L prepared Detection Reagent A. Incubate 1 hour at 37° C;
4. Aspirate and wash 3 times;
5. Add 100µ L prepared Detection Reagent B. Incubate 30 minutes at 37° C;
6. Aspirate and wash 5 times;
7. Add 90µ L Substrate Solution. Incubate 10-20 minutes at 37° C;
8. Add 50µ L Stop Solution. Read at 450nm immediately.
Test principle
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Cholinergic Receptor, Muscarinic 2 (CHRM2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Cholinergic Receptor, Muscarinic 2 (CHRM2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Cholinergic Receptor, Muscarinic 2 (CHRM2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Cholinergic Receptor, Muscarinic 2 (CHRM2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Research Area
Signal transduction; Cardiovascular biology; Neuro science;

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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