SKU: WP12996 Categories: ,

LHR Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP12996-100
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Product details

Background:

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],

Specifications

Size50μL/100μL
TargetLHR
ReactivityHuman, Mouse, Rat
ApplicationsWB, IF, ELISA, IHC
MW(Calculated)
MW(Observed)80kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000; IHC 1:50-300; IF 1:200-1:1000; ELISA 1:2000-20000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human LSHR. AA range:621-670
SpecificityLHR Polyclonal Antibody detects endogenous levels of LHR protein.
Gene NameLHCGR LCGR LGR2 LHRHR
Protein NameLutropin-choriogonadotropic hormone receptor
Other NameLHCGR; / LCGR; / LGR2; / LHRHR; / Lutropin-choriogonadotropic hormone receptor; / LH/CG-R; / Luteinizing hormone receptor; / LHR; / LSH-R
SpeciesHuman
Gene ID3973
UniprotP22888,
Species.1Mouse
Gene ID.116867
Uniprot.1P30730,
Species.2Rat
Gene ID.225477
Uniprot.2P16235
Cellular LocalizationCell membrane; Multi-pass membrane protein .
Tissue ExpressionGonadal and thyroid cells.
Signaling_pathwayOrganismal Systems >> Endocrine system >> Prolactin signaling pathway;Environmental Information Processing >> Signal transduction >> Calcium signaling pathway;Environmental Information Processing >> Signal transduction >> cAMP signaling pathway
Research Areas>>Calcium signaling pathway; / >>cAMP signaling pathway; / >>Neuroactive ligand-receptor interaction; / >>Ovarian steroidogenesis; / >>Prolactin signaling pathway
FunctionAlternative 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. FSH/LSH/TSH subfamily.,similarity:Contains 7 LRR (leucine-rich) repeats.,tissue specificity:Gonadal and thyroid cells.,
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