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LHR Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-72558

  • Amount:

    100ul

  • Price:

    225$

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human LSHR. AA range:621-670

  • Source:

    Polyclonal, Rabbit

  • Western Blot analysis of A549 cells using LHR Polyclonal Antibody

  • Gene Name:

    LHCGR

  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. Not yet tested in other applications.

  • Background:

    luteinizing hormone/choriogonadotropin receptor(LHCGR) Homo sapiens This gene encodes the receptor for both luteinizing hormone and choriogonadotropin. This receptor belongs to the G-protein coupled receptor 1 family, and its activity is mediated by G proteins which activate adenylate cyclase. Mutations in this gene result in disorders of male secondary sexual character development, including familial male precocious puberty, also known as testotoxicosis, hypogonadotropic hypogonadism, Leydig cell adenoma with precocious puberty, and male pseudohermaphtoditism with Leydig cell hypoplasia. [provided by RefSeq, Jul 2008],

  • Protein Name:

    Lutropin-choriogonadotropic hormone receptor

  • Human Gene Id:

    3973

  • Human Swiss Prot No:

    P22888

  • Mouse Gene Id:

    16867

  • Mouse Swiss Prot No:

    P30730

  • Rat Gene Id:

    25477

  • Rat Swiss Prot No:

    P16235

  • Specificity:

    LHR Polyclonal Antibody detects endogenous levels of LHR protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    LHCGR; LCGR; LGR2; LHRHR; Lutropin-choriogonadotropic hormone receptor; LH/CG-R; Luteinizing hormone receptor; LHR; LSH-R

  • MolecularWeight(Da):

    78616

  • Observed Band(KD):

    80

  • Function:

    alternative products:Additional isoforms seem to exist,disease:Defects in LHCGR are a cause of familial male precocious puberty (FMPP) [MIM:176410]; also known as testotoxicosis. In FMPP the receptor is constitutively activated.,disease:Defects in LHCGR are a cause of Leydig cell hypoplasia (LCH) [MIM:152790]. LCH is an autosomal recessive disease characterized by male pseudohermaphroditism. In LCH the testes are small with marked immaturity of the Leydig cells which correlates with undetectable plasma testosterone levels and elevated gonadotropins.,function:Receptor for lutropin-choriogonadotropic hormone. The activity of this receptor is mediated by G proteins which activate adenylate cyclase.,online information:Glycoprotein-hormone Receptors Information System,similarity:Belongs to the G-protein coupled receptor 1 family.,similarity:Belongs to the G-protein coupled receptor 1 family.

  • Subcellular Location:

    endosome,plasma membrane,integral component of plasma membrane,integral component of membrane,

  • Expression:

    Ovary,Thyroid,

  • Immunofluorescence analysis of A549 cells, using LSHR Antibody. The picture on the right is blocked with the synthesized peptide.

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Catalog Number

  • Amount:100ul
  • Price:225$

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LHR Polyclonal Antibody | EnoGene Biotech Co. Ltd