
Rabbit Anti-ChRM2 Polyclonal Antibody #abs119939
Please note that the price mentioned above is for your reference only. For detailed pricing information, kindly get in touch with our seller, Vecent. We encourage you to contact Vecent for accurate and specific pricing details. Data Examples Tissue/cell: rat brain tissue; 4%...
Description
Catalog-specification | Delivery time | USD price |
abs119939-50ul | In Stock | 201 |
abs119939-100ul | In Stock | 301 |
Please note that the price mentioned above is for your reference only. For detailed pricing information, kindly get in touch with our seller, Vecent. We encourage you to contact Vecent for accurate and specific pricing details.
Overview | |
Other names | The receptor known as Muscarinic Acetylcholine Receptor 2, also referred to as 7TM receptor, is a crucial component involved in the acetylcholine signaling pathway. It is responsible for mediating the effects of acetylcholine in various cells and tissues. With the human gene being denoted as CHRM2, this receptor plays a significant role in cardiac function, particularly in the isoform labeled as a. Other aliases for this receptor include ACM2_HUMAN, Acm2, Cholinergic receptor muscarinic 2, and Cholinergic receptor, muscarinic 2a. It is worth noting that CHRM2 is also known by several other names such as CM2, FLJ43243, M2, HM2, MGC120006, MGC120007, Muscarinic acetylcholine receptor M2, and Muscarinic M2 receptor. Overall, the Muscarinic Acetylcholine Receptor 2 represents a crucial molecular target involved in cholinergic signaling pathways with diverse implications in physiological and pathological processes. |
Source | Rabbit |
Specificity | ChRM2 |
Species Reactivity | Human;Mouse;Rat;Chicken;Dog;Pig;Cow; |
Application | The dilutions for WB are 1:500-2000, for ELISA are 1:500-1000, for IHC-P are 1:400-800, for IHC-F are 1:400-800, for Flow-Cyt are 1μg/Test, for ICC are 1:100-500, and for IF are 1:100-500 (with antigen retrieval required for paraffin sections). Please note that the following text is generated based on the original information but rearranged for a different presentation: |
Immunogen | A synthetic peptide derived from the 168-192 amino acid region of human ChRM2 (168-250/466) has been conjugated with KLH. If you rearrange this information, it can be stated that KLH-conjugated synthetic peptide has been developed from the human ChRM2 (168-192aa) region, precisely from 168-250/466 amino acid sequence. |
Properties | |
Concentration | 1mg/ml |
Purification | affinity purified by Protein A |
Clonality | Polyclonal Antibody |
Isotype | IgG |
Stability & Storage | To maintain quality, it is recommended to store the product at a temperature of -20 °C for a duration of one year. It is important to avoid subjecting the product to repeated freeze and thaw cycles. |
Storage buffer | In a solution of pH7.4 TBS with a concentration of 0.01M, there is a 1% presence of BSA along with 0.03% Proclin300 and 50% Glycerol. This composition is aimed at ensuring that the solution remains stable and effective in carrying out its intended function. The presence of these components ensures that the solution is not affected by external factors and can maintain its structure over a prolonged period. With this composition, the solution can be used effectively for various applications. |
Research area | Neurobiology cell membrane receptor |
Target | |
Background | Muscarinic cholinergic receptors, which are part of the G protein-coupled receptor family, exhibit functional diversity based on their interaction with acetylcholine. These receptors play a role in various cellular responses including the inhibition of adenylate cyclase, degradation of phosphoinositide, and mediation of potassium channels. They have a significant impact on the effects of acetylcholine in both the central and peripheral nervous systems. In particular, muscarinic cholinergic receptor 2 is involved in regulating bradycardia (a slower heart rate) and reducing cardiac contractility. This gene has been found to have multiple alternatively spliced transcript variants. This information is based on the findings provided by RefSeq in July 2008. |
Celluar localization | Cell membrane |
UniPort | P08172 |
Data Examples

Tissue/cell: rat brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
Antigen retrieval: citrate buffer, Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer at 37℃ for 20 min;
Incubation: Anti-ChRM2 Polyclonal Antibody, Unconjugated secondary primary antibody 1:200, overnight at 4°C, followed by conjugation to the secondary antibody and DAB staining

Tissue/cell: human colon carcinoma; 4% Paraformaldehyde-fixed and paraffin-embedded;
Antigen retrieval: citrate buffer, Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer at 37℃ for 20 min;
Incubation: Anti-ChRM2 Polyclonal Antibody, Unconjugated secondary primary antibody 1:200, overnight at 4°C, followed by conjugation to the secondary antibody and DAB staining

Blank control: Hela(blue).
Primary Antibody:Rabbit Anti- ChRM2 antibody, Dilution: 1μg in 100 μL 1X PBS containing 0.5% BSA;
Isotype Control Antibody: Rabbit IgG ,used under the same conditions );
Secondary Antibody: Goat anti-rabbit IgG-PE(white blue), Dilution: 1:200 in 1 X PBS containing 0.5% BSA.
Protocol
The cells were fixed with 2% paraformaldehyde (10 min) , then permeabilized with 90% ice-cold methanol for 30 min on ice. antibody were incubated for 30 min on the ice, followed by 1 X PBS containing 0.5% BSA + 1 0% goat serum (15 min) to block non-specific protein-protein interactions. Then the Goat Anti-rabbit IgG/PE antibody was added into the blocking buffer mentioned above to react with the primary antibody of (abs119939) at 1/200 dilution for 30 min on ice. Acquisition of 20,000 events was performed.
This product is for research use only, not for use in diagnostic prodecures or in human.
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