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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
"-20°C/-80°C"
- 保质期:
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
- 英文名:
Customized Geobacillus sp. mscL Protein (in vitro E.coli)
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 规格:
20ug
Alternative Name(s)
Large-conductance mechanosensitive channelEditorial/Sponsord
EditorialUniprot ID
C5DA22Gene Names
mscLOrganism
Geobacillus sp.AASequence
MWKEFKEFAMRGNVVDLAVGVIIGGAFGKIVSSLVNDILMPLVGLLLGGVDFSGLSWKFG KAVVKYGMFIQTVVDFFIISFSIFVFVKVLNKLYWHNKKEEEIKDTAPTLTKEEELLMEI RDLLKQQRETRExpression Region
1-131aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1420Purity
Greater than 85% as determined by SDS-PAGE.Storage Buffer
Tris/PBS-based buffer, 6% TrehaloseStorage
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself. Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.Endotoxin
Not Test. Endotoxin removal service is available for free upon you request.产品类型
Transmembrane-Protein备注
**产品信息可能有变动,请以官网信息为准
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文献和实验**产品信息可能有变动,请以官网信息为准
Generation and Characterization of Bispecific Tandem Diabodies for Tumor Therapy
( 3 , 4 ). However, the immunogenicity of BsAb derived from rodent monoclonal antibodies (MAbs) is a major drawback for clinical use ( 5 ). They are also difficult to produce and purify in large quantities. Recent advances in recombinant antibody technology have provided
Fluorescence Quenching Methods to Study Lipid‐Protein Interactions
Powl, A.M., East, J.M., and Lee, A.G. 2005. Heterogeneity in the binding of lipid molecules to the surface of a membrane protein: Hot‐spots for anionic lipids on the mechanosensitive channel of large conductance MscL and effects
Strategies to Optimize Protein Expression in E. coli
., Cantor, E.J., Liao, W., Xu, M.Q., and Benner, J. 1998. Utilizing the C‐terminal cleavage activity of a protein splicing element to purify recombinant proteins in a single chromatographic step. Nucleic Acids Res. 26:5109‐5115
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