GHR rabbit pAb
This gene encodes a member of the type I Cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. In humans and rabbits, but not rodents, growth hormone binding protein (GHBP) is generated by proteolytic cleavage of the extracellular ligand-binding domain from the mature growth hormone receptor protein. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011],
Product Specifications
Background
Product Name Alternative
GHR; Growth hormone receptor; GH receptor; Somatotropin receptor
UniProt
P10912
Swiss Prot
P10912
Reactivity
Human; Mouse; Rat
Immunogen
The antiserum was produced against synthesized peptide derived from the N-terminal region of human GHR. AA range:21-70
Target
GHR
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
Buffer
-20°C/1 year
Molecular Weight
140kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
140kD
Fragment
IgG
Subcellular Location
Other Product Names
GHR; Growth hormone receptor; GH receptor; Somatotropin receptor
Gene ID (Human)
2690
Available Sizes
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items