G-CSF Receptor, Recombinant, Human (G-CSFR, GCSFR, CSF3R, Granulocyte Colony-stimulating Factor Receptor, G-CSF-R, CD114)

Cat# G8950-51A-50ug

Size : 50ug

Brand : US Biological



G8950-51A Rabbit Anti-G-CSF Receptor, Recombinant, Human (G-CSFR, GCSFR, CSF3R, Granulocyte Colony-stimulating Factor Receptor, G-CSF-R, CD114)

Clone Type
Polyclonal
Swiss Prot
Q99062
Grade
Highly Purified
Shipping Temp
Blue Ice
Storage Temp
-20°C

Granulocyte Colony Stimulating Factor (G­CSF) is a pleiotropic cytokine best known for its specific effects on the proliferation, differentiation, and activation of hematopoietic cells of the neutrophilic granulocyte lineage. G­CSF plays an important role in defense against infection, in inflammation and repair, and in the maintenance of steady state hematopoiesis. Recombinant human G­CSF has been approved for the amelioration of chemotherapy induced neutropenia as well as for severe chronic neutropenia following marrow transplant. Cell activation by G­CSF is mediated by a type I membrane protein belonging to the cytokine receptor superfamily. Human G­CSF R is 863 amino acids (aa) in length, with a 604 aa extracellular domain, a 26 aa transmembrane domain, and a 183 aa cytoplasmic domain that include a 23 amino acid signal sequence. As a result of alternative splicing, at least four isoforms of G­CSF R that differ in their C­terminal region exist. Isoform 2 lacks the transmembrane region and may represent a soluble form of the receptor; however the existence of soluble G­CSF R in human serum has not been reported (1). Mutations have been found in the gene encoding G­CSF R in some patients with severe congenital neutropenia. These mutations typically led to a truncation in the cytoplasmic domain of the G­ CSF R leading to maturation arrest of neutrophil precursors in the bone marrow and neutropenia in peripheral blood (2). Human and mouse G­CSF R have a homology of 62.5%.||G­CSF R is expressed in mature neutrophils, neutrophilic precursors, myeloid leukemia cells, and placenta. Binding of G­CSF to its receptor induces dimerization or oligomerization of the receptor activating cytoplasmic tyrosine kinases. Signal transduction from pathways that involve Janus tyrosine kinases/signal transducer and activator of transcription proteins (Jak1, Jak2, and Tyk2/STAT3, STAT3, and STATG), src­related protein tyrosine kinases (Lyn and Syk), Ras/MAP kinase, and phosphatidylinositol have been reported to be activated upon G­CSF stimulation (1).||Recombinant protein corresponding to Glu25-Pro621 from human G-SCFR from murine myeloma cell line, NS0-derived. Swiss/UniProt Accession: Q99062.||SDS­-PAGE: |~95-­105kD, reducing conditions||Activity: |Measured by its ability to inhibit the G-CSF-induced proliferation of NFS-60 mouse myeloid cells. The ED50 is typically 1-4ug/ml in the presence of 0.125ng/ml of rhG-CSF.|Storage and Stability:|Lyophilized powder may be stored at -20°C. Stable for 12 months after receipt at -20°C. Reconstitute with sterile PBS. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Reconstituted product is stable for 6 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.

Applications
Source: Recombinant, NS0 cells|Purity: ≥97%, by SDS­-PAGE under reducing conditions and visualized by silver stain. Endotoxin: ≤1.0 EU/ug (LAL)|Concentration: ~0.1mg/ml (after reconstitution) |Form: Supplied as a lyophilized powder in PBS, pH 7.4, 50ug BSA. Reconstitute with 500ul sterile PBS, >0.1% human or bovine serum albumin.||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Form
Supplied as a lyophilized powder in PBS, pH 7.4, 50ug BSA. Reconstitute with 500ul sterile PBS, >0.1% human or bovine serum albumin.
Purity
≥97%, by SDS­-PAGE under reducing conditions and visualized by silver stain. Endotoxin: ≤1.0 EU/ug (LAL)
References
1. Nicola, N.A., in Cytokine Reference, (2001) Oppenhiem, J.J. and M. Feldmann, eds. Academic Press p. 1935. 2. Mitsui, T. et. al. (2003) Blood. 101:2990.|3. Nagata S (1986) Nature 319, 415- 418. 4. Develin JJ (1987) J. Leukocyte Biol. 41, 302-306. 35 Souza LM (1986) Science 232, 61-66.