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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 Sinorhizobium fredii NGR_a00830 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)
Putative exopolysaccharide production repressor protein y4xQEditorial/Sponsord
EditorialUniprot ID
P55698Gene Names
NGR_a00830Organism
Sinorhizobium frediiAASequence
MSFGIFHRILWLFLCANTLIVYLVTGSISDAVVTTMVGSLLLQLTYFANVLFLLWRAHCA RRARQTTGQFHGEEQPGDPRIAGTHGRTDGDPCFEDEDSRExpression Region
1-100aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1382Purity
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
A Practical Guide for using the AdEasy System
I. Introduction Summary Recombinant adenoviruses provide a versatile system for gene expression studies and therapeutic applications. We here report a strategy which simplifies the generation and production
Recombinant Protein Production in Antarctic Gram-Negative Bacteria
was not only produced but also efficiently secreted by the recombinant Ph TAC125 cells. The described expression system represents the first example of heterologous protein production based on a true cold-adapted replicon.
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
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