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Human G-CSF+Cell Based Assay.jpg Human G-CSF+Cell Based Assay.jpg Induces proliferation in NFS-60 cells. ED50: 0.03 ng/ml (Regularly tested).

Induces proliferation in NFS-60 cells. ED50: 0.03 ng/ml (Regularly tested).

Human G-CSF+SDS-PAGE.jpg Human G-CSF+SDS-PAGE.jpg Greater than 95% as determined by reducing SDS-PAGE.

Greater than 95% as determined by reducing SDS-PAGE.

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Recombinant Human G-CSF is a human-derived protein expressed in E. coli without any tags. This 20 kD glycoprotein contains an internal disulfide bond and functions as the most potent terminal differentiation inducer within the granulocyte colony-stimulating factor family. It promotes the survival, proliferation, and differentiation of neutrophil precursors, and activates the function of mature neutrophils. Its synthesis is regulated by multiple factors.

Synonyms: Recombinant Human G-CSF; Granulocyte Colony-Stimulating Factor; G-CSF

4.5 *For Research Use Only !

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Product Details of Human G-CSF

M.W : 18.8 KDa
SMILES Code : NONE
Synonyms :
Recombinant Human G-CSF; Granulocyte Colony-Stimulating Factor; G-CSF

Safety of Human G-CSF

Isoform Comparison

Biological Activity

Description
Human Granulocyte-Colony-Stimulating Factor (G-CSF) is 20 kD glycoprotein containing internal disulfide bonds. It induces the survival, proliferation, and differentiation of neutrophilic granulocyte precursor cells and it functionally activates mature blood neutrophils. Among the family of colony-stimulating factors, G-CSF is the most potent inducer of terminal differentiation to granulocytes and macrophages of leukemic myeloid cell lines. The synthesis of G-CSF can be induced by bacterial endotoxins, TNF, Interleukin-1, and GM-CSF. Prostaglandin E2 inhibits the synthesis of G-CSF. In epithelial, endothelial, and fibroblastic cells secretion of G-CSF is induced by Interleukin-17.
Protein Species Human
Expression System E.coli
Tag Tag free
Protein Expression Interval Thr31-Pro204
Protein ID P09919-2
Endotoxin < 0.01 EU/µg as determined by LAL test.
Characteristics Lyophilized powder
Formulation Description Lyophilized from a 0.2 μm filtered solution of 10mM HAc-NaAc, 150mM NaCl, 0.004% Tween 80, 5% Mannitol, pH 4.0.
Reconstitution Method Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
For long-term storage, it is recommended to dilute the product further with a solution containing carrier proteins (e.g., 0.1% BSA, 10% FBS, or 5% HSA). For serum-free cultures or in vivo animal experiments where BSA, FBS, or HSA cannot be present in the cytokine preparation, trehalose may be used as an alternative carrier. Aliquots should be stored frozen at -20°C to -80°C.
Note: Low-adsorption tubes are recommended for aliquot storage, and repeated freeze-thaw cycles should be avoided. The dilution concentration for aliquoting should not be lower than 10 μg/mL, and the aliquot volume should be no less than 10 μL.
Aliquoted protein remains stable for up to 3 months when stored at ≤ -20°C.
 

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