Glucagon Receptor Antibody
Purified Rabbit Polyclonal Antibody (Pab)
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Application ![]()
| WB, IHC-P |
---|---|
Primary Accession | P47871 |
Reactivity | Human, Rat |
Host | Rabbit |
Clonality | Polyclonal |
Calculated MW | 54009 Da |
Gene ID | 2642 |
---|---|
Other Names | Glucagon receptor, GL-R, GCGR |
Dilution | WB~~1:1000 IHC-P~~N/A |
Format | 0.01M PBS, pH 7.2, 0.09% (W/V) Sodium azide, Glycerol 50% |
Storage | Store at -20 °C.Stable for 12 months from date of receipt |
Name | GCGR |
---|---|
Function | G-protein coupled receptor for glucagon that plays a central role in the regulation of blood glucose levels and glucose homeostasis. Regulates the rate of hepatic glucose production by promoting glycogen hydrolysis and gluconeogenesis. Plays an important role in mediating the responses to fasting. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Promotes activation of adenylate cyclase. Besides, plays a role in signaling via a phosphatidylinositol-calcium second messenger system. |
Cellular Location | Cell membrane; Multi-pass membrane protein. Note=Is rapidly internalized after ligand-binding |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
G-protein coupled receptor for glucagon that plays a central role in the regulation of blood glucose levels and glucose homeostasis. Regulates the rate of hepatic glucose production by promoting glycogen hydrolysis and gluconeogenesis. Plays an important role in mediating the responses to fasting. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Promotes activation of adenylate cyclase. Besides, plays a role in signaling via a phosphatidylinositol-calcium second messenger system.
REFERENCES
Macneil D.J.,et al.Biochem. Biophys. Res. Commun. 198:328-334(1994).
Lok S.,et al.Gene 140:203-209(1994).
Menzel S.,et al.Genomics 20:327-328(1994).
Buggy J.J.,et al.Diabetes 46:1400-1405(1997).
Ruckert C.,et al.J. Biol. Chem. 281:2306-2316(2006).

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