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重組人粒細胞集落刺激因子(源自CHO) (rHuCHO-G-CSF)

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CYT-329重組人粒細胞集落刺激因子(源自CHO) (rHuCHO-G-CSF) 2μg/10μg/1mg Prospec

 

 

Background :
 A glycoprotein of MW 20 kDa containing internal disulfide bonds. It induces the survival, proliferation, and differentiation of neutrophilic granulocyte precursor cells and 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 .

 
Description :
 Recombinant Human Granulocyte Colony Stimulating Factor is a glycosylated, polypeptide chain containing 174 amino acids and having a molecular mass of 20 KD.
Human G-CSF is purified by proprietary chromatographic techniques.

 
Physical Appearance:
 Sterile Filtered White lyophilized (freeze-dried) powder.

 
Formulation:
 Human G-CSF was lyophilized from a concentrated (1mg/ml) solution containing 10mM Hydrochloric Acid pH=6.5, 0.4mg tween 20, 100mg mannitol, 160 mg L-arginine, 40 mg phenylalanin and 4mg methionin.
Solubility:
 It is recommended to reconstitute the lyophilized G-CSF in sterile 18MO-cm H2O not less than 100µg/ml, which can then be further diluted to other aqueous solutions.

 
Stability:
 
 Lyophilized G-CSF although stable at room temperature for 3 weeks, should be stored desiccated below -18 C. Upon reconstitution G-CSF should be stored at 4 C between 2-7 days and for future use below -18 C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).
Please avoid freeze-thaw cycles.

 
Purity:
 Greater than 98.0% as determined by:
(a) Analysis by RP-HPLC.
(b) Anion-exchange FPLC.
(c) Analysis by reducing and non-reducing SDS-PAGE Silver Stained.

 
Amino-Acid Sequence :
 The sequence of the first five N-terminal amino acids was determined and was found to be
Thr-Pro-Leu-Gly-Pro.

 
Dimers and aggregates:
 Less than 1% as determined by silver-stained SDS-PAGE gel analysis.

 
Biological Activity:
 ProSpec's G-CSF is fully biologically active when compared to standard. The ED50, calculated by the dose-dependant proliferation of murine NFS-60 indicator cells (measured by 3H-thymidine uptake) is less then 0.1 ng/ml, corresponding to a Specific Activity of 1.27 x 108 IU/mg.

 
Endotoxin:
 Less than 0.1 ng/µg (IEU/µg) of Recombinant Human Granulocyte Colony Stimulating Factor.

 
Protein content:
 G-CSF protein quantitation was carried out by two independent methods:
1. UV spectroscopy at 280 nm using the absorbency value of 0.815 as the extinction coefficient for a 0.1% (1mg/ml) solution. This value is calculated by the PC GENE computer analysis program of protein sequences (InliGenetics).
2. Analysis by RP-HPLC, using a calibrated solution of Recombinant Human Granulocyte Colony Stimulating Factor as a Reference Standard.

 
 
Usage:
 Prospec's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.

 


 
Latest Publications:
 1. Granulocyte colony-stimulating factor and acute myocardial infarction.

JAMA 2006 Oct 25;296(16):1968; auth or reply 1968-9

2. Granulocyte colony-stimulating factor and acute myocardial infarction.

JAMA 2006 Oct 25;296(16):1967-8; author reply 1968-9

3. Autocrine growth by granulocyte colony-stimulating factor in malignant mesothelioma.

Ann Thorac Surg 2006 Nov;82(5):1904-6

4. Granulocyte colony-stimulating factor.

CMAJ 2006 Oct 24;175(9):1095; author reply 1095-6

5. Granulocyte colony-stimulating factor.

CMAJ 2006 Oct 24;175(9):1095; author reply 1095-6

6. Weekly cisplatin, epirubicin, and paclitaxel with granulocyte colony-stimulating factor support vs triweekly epirubicin and paclitaxel in locally advanced breast cancer: final analysis of a sicog phase III study.

Br J Cancer 2006 Oct 23;95(8):1005-12
 


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