Revision 1

#10424Store at -20C

Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
Applications:

WB, IP, FC-L

REACTIVITY:

H

SENSITIVITY:

Endogenous

MW (kDa):

50-80, 110-140

Source/Isotype:

Rabbit IgG

UniProt ID:

#Q99062

Entrez-Gene Id:

1441

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:100
Flow Cytometry (Live) 1:50 - 1:200

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.

Specificity / Sensitivity

G-CSF-R (E8E7D) Rabbit mAb recognizes endogenous levels of total G-CSF-R protein.

Species Reactivity:

Human

Source / Purification

Monoclonal antibody is produced by immunizing animals with recombinant protein specific to the extracellular domain of human G-CSF-R protein.

Background

Granulocyte colony-stimulating factor receptor (G-CSF-R) is a transmembrane protein comprised of an immunoglobulin-like (Ig-like) domain, a cytokine receptor-homologous (CRH) domain, and three fibronectin type III (FN III) domains (1). G-CSF-R is expressed on all granulocytic lineages, including progenitor cells, and has been detected on monocytes, T and B lymphocytes, as well as non-hematopoietic tissues including cardiomyocytes and neural stem cells (2-6). The primary ligand for G-CSF-R is the cytokine granulocyte colony-stimulating factor (G-CSF). G-CSF-R has no intrinsic tyrosine kinase activity; ligand binding induces conformational changes in the receptor, leading to activation of the Jak/Stat, PI3K/Akt, and MAPK pathways (7-10). G-CSF induces differentiation and proliferation of myeloid progenitor cells into neutrophils (11). Multiple diseases have been associated with mutations of the G-CSF-R gene, CSF3R, including severe congenital neutropenia (SCN), chronic neutrophilic leukemia (CNL), and atypical chronic myeloid leukemia (aCML) (12).

  1. Fukunaga, R. et al. (1991) EMBO J 10, 2855-65.
  2. Nicola, N.A. and Metcalf, D. (1984) Proc Natl Acad Sci U S A 81, 3765-9.
  3. Boneberg, E.M. et al. (2000) Blood 95, 270-6.
  4. Morikawa, K. et al. (2002) Br J Haematol 118, 296-304.
  5. Harada, M. et al. (2005) Nat Med 11, 305-11.
  6. Schneider, A. et al. (2005) J Clin Invest 115, 2083-98.
  7. Fukunaga, R. et al. (1993) Cell 74, 1079-87.
  8. Nicholson, S.E. et al. (1994) Proc Natl Acad Sci U S A 91, 2985-8.
  9. Zhu, Q.S. et al. (2006) Blood 107, 1847-56.
  10. Bashey, A. et al. (1994) Blood 83, 949-57.
  11. Touw, I.P. et al. (2013) Hematol Oncol Clin North Am 27, 61-73, viii.
  12. Dwivedi, P. and Greis, K.D. (2017) Exp Hematol 46, 9-20.

Species Reactivity

Species reactivity is determined by testing in at least one approved application (e.g., western blot).

Western Blot Buffer

IMPORTANT: For western blots, incubate membrane with diluted primary antibody in 5% w/v BSA, 1X TBS, 0.1% Tween® 20 at 4°C with gentle shaking, overnight.

Applications Key

WB: Western Blotting IP: Immunoprecipitation FC-L: Flow Cytometry (Live)

Cross-Reactivity Key

H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

Trademarks and Patents

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
XP is a registered trademark of Cell Signaling Technology, Inc.
All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

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