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Phospho-CSF-1R/M-CSF-R (Tyr708) (D5F4Y) Rabbit mAb #14591

Filter:
  • WB
  • IP
Western blot analysis of extracts from GDM-1 cells, serum-starved overnight and untreated (-) or treated with Human Macrophage Colony Stimulating Factor (hM-CSF) #8929 (100 ng/ml, 5 min; +), using Phospho-CSF-1R/M-CSF-R (Tyr708) (D5F4Y) Rabbit mAb (upper) and CSF-1R/M-CSF-R Antibody #3152 (lower).

To Purchase # 14591

Cat. # Size Qty. Price
14591T 20 µl
$173
14591S 100 µl
$401

Supporting Data

REACTIVITY H
SENSITIVITY Endogenous
MW (kDa) 175
Source/Isotype Rabbit IgG
Application Key:
  • WB-Western Blotting 
  • IP-Immunoprecipitation 
Species Cross-Reactivity Key:
  • H-Human 
  • Related Products

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:100

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

Protocol

Specificity / Sensitivity

Phospho-CSF-1R/M-CSF-R (Tyr708) (D5F4Y) Rabbit mAb recognizes endogenous levels of CSF-1R/M-CSF-R only when phosphorylated at Tyr708. This antibody may cross-react with other activated protein tyrosine kinases such as phospho-Src.

Species Reactivity:

Human

The antigen sequence used to produce this antibody shares 100% sequence homology with the species listed here, but reactivity has not been tested or confirmed to work by CST. Use of this product with these species is not covered under our Product Performance Guarantee.

Species predicted to react based on 100% sequence homology:

Mouse, Rat

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr708 of human CSF-1R/M-CSF-R protein.

Background

Macrophage-colony stimulating factor (M-CSF, CSF-1) receptor is an integral membrane tyrosine kinase encoded by the c-fms proto-oncogene. M-CSF receptor is expressed in monocytes (macrophages and their progenitors) and drives growth and development of this blood cell lineage (1-3). Binding of M-CSF to its receptor induces receptor dimerization, activation, and autophosphorylation of cytoplasmic tyrosine residues used as docking sites for SH2-containing signaling proteins (4). There are at least five major tyrosine autophosphorylation sites. Tyr723 (Tyr721 in mouse) is located in the kinase insert (KI) region. Phosphorylated Tyr723 binds the p85 subunit of PI3 kinase as well as PLCγ2 (5). Phosphorylation of Tyr809 provides a docking site for Shc (5). Overactivation of this receptor can lead to a malignant phenotype in various cell systems (6). The activated M-CSF receptor has been shown to be a predictor of poor outcome in advanced epithelial ovarian carcinoma (7) and breast cancer (8).

Tyr708 (Tyr706 in mouse) is located in the KI region of M-CSF receptor. Phosphorylation of Tyr708 may influence the binding of PI3 kinase to the activated M-CSF receptor (9).

Pathways

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For Research Use Only. Not For Use In Diagnostic Procedures.
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