GeneBio Systems
Recombinant Growth Hormone Receptor/GHR/GHBP Monoclonal Antibody
Recombinant Growth Hormone Receptor/GHR/GHBP Monoclonal Antibody
SKU:AN300463P
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Size::20μL
Storage:This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.
Shipping:Ice bag
Exp date:12 months
Category ID_II:Primary Antibodies
Category ID_III:Recombinant Antibodies;Monoclonal Antibodies
Abbreviation:GHR
Target Synonym:Small-inducible cytokine A;T lymphocyte-secreted protein I;SCYA;GH receptor;GH-binding protein;GHBP;SCYA1;Serum binding protein;Small-inducible cytokine A1;T lymphocyte-secreted protein I-309;Ghr;GHR/BP;Growth Hormone Receptor
Research Areas:
Conjugation:Unconjugated
Host:Rabbit
Species reactivity:Mouse
Application:IHC-P
Isotype:IgG
Clonality:Monoclonal
Clone NO.:8B9
UNIProt ID:P16882
Accession:
Background:Growth hormone receptor, also known as GH receptor and GHR, is a single-pass type I membrane protein which belongs to thetype I cytokine receptor family and type 1 subfamily. GHR contains onefibronectin type-III domain. Growth hormone receptor/GHR is expressed in various tissues with high expression in liver and skeletal muscle. Isoform4of GHR is predominantly expressed in kidney, bladder, adrenal gland and brain stem. Isoform1 expression of GHR in placenta is predominant in chorion and decidua. Isoform4is highly expressed in placental villi. Isoform2of GHR is expressed in lung, stomach and muscle. Growth hormone receptor/GHR is a receptor for pituitary gland growth hormone. It is involved in regulating postnatal body growth. On ligand binding, it couples to the JAK2/STAT5 pathway. Isoform2of GHR up-regulates the production of GHBP and acts as a negative inhibitor of GH signaling. Defects in GHR are a cause of Laron syndrome (LARS) which is a severe form of growth hormone insensitivity characterized by growth impairment, short stature, dysfunctional growth hormone receptor, and failure to generate insulin-like growth factor I in response to growth hormone. Defects in GHR may also be a cause of idiopathic short stature autosomal (ISSA) which is defined by a subnormal rate of growth.
Concentration:1 mg/mL
Immunogen:Recombinant Mouse Growth Hormone Receptor/GHR/GHBP protein
Buffer:0.2 μm filtered solution in PBS
Purification method:Protein A
Dilution:IHC-P 1:50-1:200
Calculated MW:
ObservedMW:
