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真核翻译起始因子4E结合蛋白1(EIF4EBP1)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
YB80481Ra01
Eukaryotic Translation Initiation Factor 4E Binding Protein 1 (EIF4EBP1)
Organism: Rattus norvegicus (Rat)
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: Eukaryotic Translation Initiation Factor 4E Binding Protein 1
Gene Names: EIF4EBP1
Size: 100µg
Source: Recombinant
Expression Host: E.coli
Function: Regulates eIF4E activity by preventing its assembly into the eIF4F complex. Mediates the regulation of protein translation by hormones, growth factors and other stimuli that signal through the MAP kinase and mTORC1 pathways.
Tissue Specificity: Expressed in all tissues examined; highest levels in fat and skeletal tissue, lowest levels in kidney.
[ PROPERTIES ]
Residues: Ser2~Ile117 (Accession # Q62622), with a N-terminal His-tag.
Grade & Purity: >97%, 13.79 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: 13.79 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-SAGSSCSQT PSRAIPTRRV ALGDGVQLPP GDYSTTPGGT LFSTTPGGTR IIYDRKFLME
CRNSPVAKTP PKDLPTIPGV TSPTSDEPPM QASQSHLHSS PEDKRAGGEE SQFEMDI
[ REFERENCES ]
1.Takabatake M, et al. (2011) In Vivo. 25(6):853-60.
2.Ohsumi M, et al. (2010) J Nutr Sci Vitaminol (Tokyo). 56(5):319-25.
3.Ayuso MI, et al. (2010) J Biol Chem. 285(45):34355-63.
4.Xu JT, et al. (2010) Brain Res.1336:46-57.
5.Ma XM, et al. (2009) Nat Rev Mol Cell Biol. 10(5):307-18.
6.Hu C., et al. (2006) Nature. 440:497-500.
7.Lin T.-A., et al. (1994) Science. 266:653-656.
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