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Ä«Å×°í¸® Chemokines
CAT.NO LGP-20-012
PRODUCT SDF-1¥á/CXCL12¥á, Human (Stromal-Cell Derived Factor-1 alpha/CXCL12 alpha)
SIZE 10ug, 100ug, 500ug
PRICE KRW 285,000, 880,000, 2,569,000
.
Technical Parameters
Synonyms SDF-1 alpha, hSDF-1 alpha, IRH, hIRH, PBSF
Species 9
Accession P48061
GeneID 6387
Source Escherichia coli.
Molecular Weight Approximately 8.0 kDa, a single non-glycosylated polypeptide chain containing 68 amino acids.
Quantity 10µg/100µg/500µg
AA Sequence KPVSLSYRCP CRFFESHVAR ANVKHLKILN TPNCALQIVA RLKNNNRQVC IDPKLKWIQE YLEKALNK
Purity > 97 % by SDS-PAGE and HPLC analyses.
Biological Activity Fully biologically active when compared to standard. The biological activity determined by a chemotaxis bioassay using PHA and rHuIL-2 activated human peripheral blood T-lymphocytes is in a concentration range of 20-80 ng/ml.
Physical Appearance Sterile Filtered White lyophilized (freeze-dried) powder.
Formulation Lyophilized from a 0.2 ¥ìm filtered concentrated solution in 20 mM PB pH 7.0, 130 mM NaCl.
Endotoxin Less than 1 EU/¥ìg of rHuSDF-1¥á/CXCL12¥á as determined by LAL method.
Reconstitution We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Reconstitute in sterile distilled water or aqueous buffer containing 0.1 % BSA to a concentration of 0.1-1.0 mg/mL. Stock solutions should be apportioned into working aliquots and stored at ¡Â -20 ¡ÆC. Further dilutions should be made in appropriate buffered solutions.
Stability & Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- 12 months from date of receipt, -20 to -70 ¡ÆC as supplied.
- 1 month, 2 to 8 ¡ÆC under sterile conditions after reconstitution.
- 3 months, -20 to -70 ¡ÆC under sterile conditions after reconstitution.
Usage This material is offered by Korea Lugen Sci for research, laboratory or further evaluation purposes. NOT FOR HUMAN USE.
Reference 1. Shirozu M, Nakano T, Inazawa J, et al. 1995. Genomics. 28:495-500.
2. Yu L, Cecil J, Peng SB, et al. 2006. Gene. 374:174-9.
3. De La Luz Sierra M, Yang F, Narazaki M, et al. 2004. Blood. 103:2452-9.
4. Charnaux N, Brule S, Hamon M, et al. 2005. FEBS J. 272:1937-51.
5. Bleul CC, Fuhlbrigge RC, Casasnovas JM, et al. 1996. J Exp Med. 184:1101-9.
6. Ara T, Nakamura Y, Egawa T, et al. 2003. Proc Natl Acad Sci U S A. 100:5319-23.
7. Askari AT, Unzek S, Popovic ZB, et al. 2003. Lancet. 362:697-703.
8. Ma Q, Jones D, Borghesani PR, et al. 1998. Proc Natl Acad Sci U S A. 95:9448-53.
9. Kryczek I, Wei S, Keller E, et al. 2007. Am J Physiol Cell Physiol. 292:C987-95.
Background CXCL12 also known as SDF-1 is belonging to the CXC chemokine family. It is encoded by the CXCL12 gene. In recently study, Human CXCL12 is expressed as six isoforms that differ only in the C-terminal tail. And all SDF-1 isoforms undergo proteolytic processing of the first two N-terminal amino acids. Contrast to the canonical sequence SDF-1¥â, SDF-1¥á is shorter by four amino acids at the C-terminal tail. On the cell surface, the receptor for this chemokine is CXCR4 and syndecan4. CXCL12 is strongly chemotactic for T-lymphocytes, monocytes, but not neutrophils. CXCL12 is a very important factor in carcinogenesis and the neovascularisation linked to tumor progression.
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