V-Ets骨髓成红细胞增多症病毒E26癌基因同源物1(ETS1)重组蛋白(Mouse,小鼠)
Recombinant V-Ets Erythroblastosis Virus E26 Oncogene Homolog 1 (ETS1)
EWSR2; p54; Protein C-ets-1
[ PROPERTIES ]
Accession: P27577
Host: E.coli
Residues: Met1~Arg243
Tags: Two N-terminal Tags, His-tag and T7-tag
Subcellular Location: Nucleus.
Purity: >90%
Endotoxin Level: <1.0EU per 1μg(determined by the LAL method).
Formulation: Supplied as lyophilized form in 20mM Tris,150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT,0.01% sarcosyl, 5% trehalose, and preservative.
Applications: SDS-PAGE; WB; ELISA; IP.
(May be suitable for use in other assays to be determined by the end user.)
Predicted isoelectric point: 4.6
Predicted Molecular Mass: 31.3kDa
Accurate Molecular Mass: 40kDa as determined by SDS-PAGE reducingconditions.
Phenomenon explanation:
The possible reasons that the actual band size differs from the predicted are as follows:
1.Splice variants: Alternative splicing may create different sized proteins from the same gene.
2. Relative charge: The composition of amino acids may affects the charge of the protein.
3. Post-translational modification: Phosphorylation, glycosylation, methylation etc.
4. Post-translation cleavage: Many proteins are synthesized as pro-proteins, and then cleavedto give the active form.
5. Polymerization of the target protein: Dimerization, multimerization etc.
[ USAGE ]
Reconstitute in sterile ddH?O
[ STORAGE AND STABILITY ]
Storage:Avoid repeated freeze/thaw cycles.
Store at 2-8°C for one month.
Aliquot and store at -80°C for 12 months.
Stability Test: The thermal stability is described by the loss rate of thetargetprotein. The loss rate was determined by accelerated thermal degradationtest,that is, incubate the protein at 37°C for 48h, and no obvious degradationandprecipitation were observed. (Referring from China Biological Products Standard,which was calculated by the Arrhenius equation.) The loss of this proteinislessthan 5% within the expiration date under appropriate storage condition.
[ SEQUENCES ]
The sequence of the target protein is listed below.
MKAAVDLKPT LTIIKTEKVD LELFPSPDME CADVPLLTPS SKEMMSQALK ATFSGFTKEQQR LGIPK DP R QW TET HV RDW VMWAV NEFS L KGV D FQKF CMSGA A L CA LGKECFLELAPDF VGDILWEHLE ILQKEDVKPY QVNGANPTYP ESCYTSDYFI SYGIEHAQCVPPSEFSEPSF ITESYQTLHP ISSEELLSLK YENDYPSVIL QDPLQTDTLQTDYFAIKQEVLTPDNMCLGR ASR
[ IDENTIFICATION ]

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