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血管抑素(ANG)重组蛋白
血管抑素(ANG)重组蛋白

血管抑素(ANG)重组蛋白The target protein is fused with a His-tag and its sequence is listed below. The first Met is an initiator amino acid. Moreover, Gly and Ser are added to improve the flexibility of N-terminus at both ends of the His-tag, which will increase t

Product Introduction


YB90007Po01


Angiogenin (ANG)


Organism: Sus scrofa; Porcine (Pig)


Instruction manual


FOR IN VITRO USE AND RESEARCH USE ONLY


NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES



1th Edition (Revised in February, 2012)



[ DESCRIPTION ]


Protein Names: Angiogenin


Gene Names: ANG


Size: 100µg


Source: Recombinant


Expression Host: E.coli


Function: May function as a tRNA-specific ribonuclease that abolishes protein synthesis by specifically hydrolyzing cellular tRNAs. Binds to actin on the surface of endothelial cells; once bound, angiogenin is endocytosed and translocated to the nucleus. Angiogenin induces vascularization of normal and malignant tissues. Angiogenic activity is regulated by interaction with RNH1 in vivo.


Subcellular Location: Secreted


[ PROPERTIES ]


Residues: Lys1~Gln123 (Accession # P31346), with a N-terminal His-tag.


Grade & Purity: >97%, 15.58 kDa as determined by SDS-PAGE reducing conditions.


Form & Buffer: Supplied as lyophilized form in PBS, pH 7.4.


Endotoxin Level: <1.0 EU per 1μg(determined by the LAL method).


Applications: SDS-PAGE; WB; ELISA;IP.


(May be suitable for use in other assays to be determined by the end user.)


Predicted Molecular Mass: 15.58 kDa


[ PREPARATION ]



Reconstitute in PBS.


[ STORAGE AND STABILITY ]


Storage: Store at 4oC for short term storage (1-2 weeks). Aliquot and store at -20oC or -80oC for long term storage. Avoid repeated freeze/thaw cycles.


Valid period: 12 months stored at -80oC.


[ BACKGROUND]


The target protein is fused with a His-tag and its sequence is listed below. The first Met is an initiator amino acid. Moreover, Gly and Ser are added to improve the flexibility of N-terminus at both ends of the His-tag, which will increase the chelating ability of the tag to Ni-Sepharose during purification.


MGHHHHHHSGSEF-KDEDRYTHFL TQHYDAKPKG RDGRYCESIM KQRGLTRPCK EVNTFIHGTR


NDIKAICNDK NGEPYNNFRR SKSPFQITTC KHKGGSNRPP CGYRATAGFR TIAVACENGL PVHFDESFII TSQ


[ REFERENCES ]


1.Bond M.D., et al. (1993) Biochim. Biophys. Acta 1162:177-186


2.Kurachi, K., et al. (1985) Biochemistry. 24: 5495-5499.


3.Rybak, S. M., et al. (1987) Biochem. Biophys. Res. Commun. 146: 1240-1248.

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