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Phospho-Ras-GRF1 (Ser916) Antibody #3321

Filter:
  • WB
Western Blotting Image 1: Phospho-Ras-GRF1 (Ser916) Antibody
Western blot analysis of extracts from COS cells, untransfected (lane 1) or transfected with either wild-type (lanes 2 and 3) or Ala916 mutant (lanes 4 and 5) Ras-GRF1, using Phospho-Ras-GRF1 (Ser916) Antibody (upper) or Ras-GRF1 Antibody #3322 (lower). Transfected COS cells were untreated or treated forskolin as indicated.(Triple HA-tagged Ras-GRF1 expressing plasmids provided by Dr. R. Mattingly, Dept. of Pharmacology, Wayne State University, Michigan.)

To Purchase # 3321

Supporting Data

REACTIVITY M
SENSITIVITY Transfected Only
MW (kDa) 155
SOURCE Rabbit
Application Key:
  • WB-Western Blotting 
Species Cross-Reactivity Key:
  • M-Mouse 
  • Related Products

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA and 50% glycerol. Store at –20°C. Do not aliquot the antibody.

Protocol

Specificity / Sensitivity

Phospho-Ras-GRF1 (Ser916) Antibody detects transfected levels of Ras-GRF1 only when phosphorylated at serine 916. This antibody does not cross-react with phosphorylated Ras-GRF2.

Species Reactivity:

Mouse

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding serine 916 of mouse Ras-GRF1. Antibodies are purified by protein A and peptide affinity chromatography.

Background

Ras activity is regulated by GAP (GTPase activating proteins) and GEFs (guanine nucleotide exchange factors). Ras-GRF1 (also known as CDC25Mm) is neuronal RasGEF and is regulated by heterotrimeric G proteins and calcium influx (1,2). Binding to calmodulin and phosphorylation stimulate Ras-GRF1 activity (1,2). Multiple PKA phosphorylation sites on Ras-GRF have been identified. Phosphorylation on the two major sites, Ser54 and Ser822, inhibits Ras-GRF activity (3). Carbachol (a muscarinic agonist)-induced phosphorylation on Ser916 is essential but not sufficient for maximal Ras-GRF activity (4). It has been reported that Ras-GRF1 also shows GEF activity toward Rac after phosphorylation by the tyrosine kinase Src (5).
For Research Use Only. Not For Use In Diagnostic Procedures.
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