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Human Insulin R/CD220 Biotinylated MAb (Clone 243524) 100 UG

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Human Insulin R/CD220 Biotinylated MAb (Clone 243524) 100 UG信息二維碼

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產(chǎn)品介紹

    基本參數(shù)

    詳細(xì)說(shuō)明

    • Species Reactivity

      Human

    • Specificity

      Detects human Insulin R/CD220 in direct ELISAs.

    • Source

      Monoclonal Mouse IgG    2B Clone # 243524

    • Purification

      Protein A or G purified from hybridoma culture supernatant

    • Immunogen

      Mouse myeloma cell line NS0-derived recombinant human Insulin R/CD220    
      His28-Lys944    
      Accession # NP_001073285

    • Formulation

      Lyophilized from a 0.2 μm filtered solution in PBS with BSA as a carrier protein.

    • Label

      Biotin

    Applications


    • Recommended    
      Concentration

      Sample

    • Flow Cytometry

      2.5 μg/10    6 cells

      Human peripheral blood monocytes


    Please Note: Optimal dilutions should be determined by each laboratory for each application.  are available in the Technical Information section on our website.

    Preparation and Storage

    • Reconstitution

      Reconstitute at 0.5 mg/mL in sterile PBS.

    • Shipping

      The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.

    • Stability & Storage

      Use a manual defrost freezer and avoid repeated freeze-thaw cycles.    

      • 12 months from date of receipt, -20 to -70 °C as supplied.

      • 1 month, 2 to 8 °C under sterile conditions after reconstitution.

      • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

    Background: Insulin R/CD220

    The Insulin Receptor (INS R) and insulin-like growth factor-1 receptor (IGF-I R) constitute a subfamily of receptor tyrosine kinases (1-4). The two receptors share structural similarity as well as overlapping intracellular signaling events, and are believed to have evolved through gene duplication from a common ancestral gene. INS R cDNA encodes a type I transmembrane single chain preproprotein with a putative 27 amino acid (aa) signal peptide. The large INS R extracellular domain is organized into two successive homologous globular domains which are separated by a cysteine-rich domain followed by three fibronectin type III domains. The intracellular region contains the kinase domain sandwiched between the juxtamembrane domain used for docking insulin-receptor substrates (IRS) and the carboxy?terminal tail that contains two phosphotyrosine-binding sites. After synthesis, the single chain INS R precursor is glycosylated, dimerized and transported to the Golgi apparatus where it is processed at a furin-cleavage site within the middle fibronectin type III domain to generate the mature disulfide-linked  alpha 2 beta 2 tetrameric receptor. The alpha subunit is localized extracellularly and mediates ligand binding while the transmembrane beta subunit contains the cytoplasmic kinase domain and mediates intracellular signaling. As a result of alternative splicing, two INS R isoforms (A and B) that differ by the absence or presence, respectively, of a 12 aa sequence in the carboxyl terminus of the alpha subunit exist. Whereas the A isoform is predominantly expressed in fetal tissues and cancer cells, the B isoform is primarily expressed in adult differentiated cells. Both the A and B isoforms bind insulin with high-affinity, but the A isoform has considerably higher affinity for IGF?I and IGF-II. Ligand binding induces a conformational change of the receptor, resulting in ATP binding, autophosphorylation, and subsequent downstream signaling. INS R signaling is important in metabolic regulation but may also contribute to cell growth, differentiation and apoptosis. Mutations in the INS R gene have been linked to insulin-resistant diabetes mellitus, noninsulin-dependent diabetes mellitus and leprechaunism, an extremely rare disorder characterized by abnormal resistance to insulin that results in a variety of distinguishing characteristics, including growth delays and abnormalities affecting the endocrine system. INS R is highly conserved between species, rat INS R shares 94% and 97% aa sequence homology with the human and mouse receptor, respectively.

    • References:

      1. Nakae, J. et al. (2001) Endoc. Rev. 22:818.

      2. De Meyts, P. and J. Whittaker (2002) Nature Rev. Drug Disc. 1:769.

      3. Kim, J.J. and D. Accili (2002) Growth Hormone and IGF Res. 12:84.

      4. Sciacca, L. et al. (2003) Endocrinology 144:2650.

    • Long Name:

      Insulin Receptor

    • Entrez Gene IDs:

      3643 (Human); 16337 (Mouse)

    • Alternate Names:

      CD 220; CD220 antigen; CD220; EC 2.7.10; EC 2.7.10.1; HHF5; INSR; Insulin R; insulin receptor; InsulinR; IR











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