Cell Signaling Technology

Product Pathways - Tyrosine Kinase / Adaptors

Phospho-M-CSF Receptor (Tyr546) Antibody #3083

m-csf   mcsf  

No. Size Price
3083S 100 µl ( 10 western blots ) ¥4,050.00 现货查询 购买询价 防伪查询
3083 carrier free & custom formulation / quantityemail request
Applications Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W 1:1000 Human,Mouse, Transfected Only 175 Rabbit

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting,

Specificity / Sensitivity

Phospho-M-CSF Receptor (Tyr546) Antibody detects transfected levels of M-CSF receptor only when phosphorylated at Tyr546. This antibody may cross-react with other tyrosine-phosphorylated protein tyrosine kinases.

磷酸化M-CSF 受体(Tyr546)的抗体仅在转染表达的M-CSF 受体的Tyr546位点发生磷酸化时能检测到。本抗体能与其它酪氨酸被磷酸化的酪氨酸激酶发生交叉反应。

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr546 of human M-CSF receptor. Antibodies are purified by protein A and peptide affinity chromatography.

多克隆抗体通过用多肽免疫动物得到,该磷酸化多肽是根据人的M-CSF 受体蛋白Tyr546附近的氨基酸序列合成的。抗体经过protein A和亲和层析纯化。

Western Blotting

Western Blotting

Western blot analysis of extracts of Bac1.2F5 cells, untreated or stimulated with CSF-1, using Phospho-M-CSF Receptor (Tyr546) Antibody (upper) or M-CSF Receptor Antibody #3152 (lower). 用抗磷酸化M-CSF 受体(Tyr546)的抗体(上)或抗M-CSF 受体的抗体#3152(下)对经过或未经CSF-1刺激的Bac1.2F5细胞的提取物进行免疫印迹检测。


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 PLC-γ 2 (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).

巨噬细胞集落刺激因子(M-CSF, CSF-1)受体是由原癌基因c-fms编码的一种膜嵌合的酪氨酸激酶。M-CSF 受体表达在单核细胞(巨噬细胞及其前体细胞)上并促进这一系列血细胞的生长和发育(1-3)。M-CSF和它的受体结合后会引起受体二聚化、激活、以及细胞质内作为含SH2信号蛋白结合位点的酪氨酸残基自磷酸化(4)。至少有5个主要的酪氨酸自磷酸化位点。Tyr723 (小鼠Tyr721)位于激酶插入(KI)区。磷酸化的Tyr723能够与PI3K激酶的p85亚基以及PLC-γ 2结合(5)。磷酸化的Tyr809能够为Shc提供停泊位点(5)。该受体的过度激活会导致各种细胞体系呈现出恶性特征(6)。激活的M-CSF 受体表明晚期上皮样卵巢癌(7)和乳腺癌预后不良(8)。

Tyr546 is a major autophosphorylation site in the juxtamembrane domain of the M-CSF receptor. Phosphorylation of Tyr546 plays an important role in the activation of M-CSF (9) and may provide a binding site for downstream signaling components (10).

Tyr546 是M-CSF受体近膜区的主要自磷酸化位点。Tyr546的磷酸化对M-CSF的活化十分重要(9)并为下游的信号分子提供结合位点(10)。

  1. Stanley, E.R. et al. (1978) Nature 274, 168-70.
  2. Byrne, P.V. et al. (1981) J Cell Biol 91, 848-53.
  3. Bourette, R.P. and Rohrschneider, L.R. (2000) Growth Factors 17, 155-66.
  4. Novak, U. et al. (1996) Oncogene 13, 2607-13.
  5. Bourette, R.P. et al. (1997) EMBO J 16, 5880-93.
  6. Morley, G.M. et al. (1999) Oncogene 18, 3076-84.
  7. Toy, E.P. et al. (2001) Gynecol Oncol 80, 194-200.
  8. Maher, M.G. et al. (1998) Clin Cancer Res 4, 1851-6.
  9. Schubert, C. et al. (2007) J. Biol. Chem. 282, 4094-4101.
  10. Joos, H. et al. (1996) J. Biol. Chem. 271, 24476-24481.

Application References

Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know!


Companion Products

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

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.

Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.

用户评论 --- 共 0


我要参与评论 :