Insulin Receptor (INSR) Antibody from ABBEXA LTD
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| Antigenic Specificity | Insulin Receptor (INSR) |
| Clone | polyclonal |
| Host Species | Rabbit |
| Reactive Species | mouse |
| Isotype | n/a |
| Format | Protein G purified |
| Size | 50 µl, 200 µl, |
| Concentration | n/a |
| Applications | ELISA, WB, IHC |
| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
| Description | INSR is a receptor that binds insulin and has a tyrosine-protein kinase activity. Autophosphorylation activates the kinase activity. This Type I mebrane protein is composed of a tetramer of 2 alpha and 2 beta chains linked by disulfide bonds. The alpha chains contribute to the formation of the ligand-binding domain, while the beta chains carry the kinase domain. After being transported from the endoplasmic reticulum to the Golgi apparatus, the single glycosylated precursor is further glycosylated and then cleaved, followed by its transport to the plasma membrane. Defects in INSR are the cause of insulin resistance of various forms, including mild insulin-resistant diabetes mellitus with acanthosis nigricans, minor physical abnormalities and sometimes polycystic ovaries. Insulin resistance associated with acanthosis nigricans, hirsutism and hyperandrogenism is referred to as insulin resistance type A. Defects in INSR are the cause of Rabson-Mendenhall syndrome, also known as Mendenhall syndrome. It is a severe insulin resistance syndrome characterized by insulin-resistant diabetes mellitus with pineal hyperplasia and somatic abnormalities. Typical features include coarse, senile-appearing facies, dental and skin abnormalities, abdominal distension, and phallic enlargement. Inheritance is autosomal recessive. Defects in INSR are the cause of leprechaunism, also known as Donohue syndrome. Leprechaunism represents the most severe form of insulin resistance syndrome, characterized by intrauterine and postnatal growth retardation and death in early infancy. Inheritance is autosomal recessive. Defects in INSR may be associated with noninsulin-dependent diabetes mellitus. |
| Immunogen | KLH-conjugated synthetic peptide between 21-52 amino acids from the N-terminal region of human INSR (Insulin Receptor). |
| Other Names | INSR, CD220, HHF5, Insulin receptor, Insulin receptor subunit alpha, Insulin receptor subunit beta, IR, INSR, INSR, INSR , INSR , CD220, CD220, CD220 , CD220 , HHF5, HHF5, HHF5 , HHF5 , Insulin receptor, Insulin receptor, Insulin receptor , Insulin receptor , Insulin receptor subunit alpha, Insulin receptor subunit alpha, Insulin receptor subunit alpha , Insulin receptor subunit alpha , Insulin receptor subunit beta, Insulin receptor subunit beta, Insulin receptor subunit beta , Insulin receptor subunit beta , IR, IR, IR , IR |
| Gene, Accession # | INSR, Gene ID: 3643, NCBI: NP_000199.2, NP_001073285.1, UniProt: P06213 |
| Catalog # | abx033580 |
| Price | please inquire |
| Order / More Info | Insulin Receptor (INSR) Antibody from ABBEXA LTD |
| Product Specific References | n/a |
ABBEXA LTD
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