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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 Saccharomyces cerevisiae YPR039W 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 uncharacterized protein YPR039WEditorial/Sponsord
EditorialUniprot ID
Q6B0W0Gene Names
YPR039WOrganism
Saccharomyces cerevisiaeAASequence
MASFDYLFHPFVPCTICPDFPLYKSPAFPSSCLHHPRLLFNDKAFCPLFLVPFPASFTRW LTFLFHLVIYNNKMHHHTYAPHIHDLRAALDTTAPQKKCPKETLHRSDHQGExpression Region
1-111aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1396Purity
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
Inducible Expression Cassettes in Yeast: GAL4
The yeast Saccharomyces cerevisiae can be grown in the laboratory with ease and at relatively low expense, and can be propagated in large scale fermentation cultures when preparation of larger amounts of a recombinant protein is desired
Heterologous Expression of Human Membrane Receptors in the Yeast Saccharomyces cerevisiae
in large-scale production-adapted cells a prerequisite for structural studies. The yeast Saccharomyces cerevisiae is a convenient host for the production of mammalian MPs for functional and structural studies. Like bacteria, they are straightforward
Optimizing Saccharomyces cerevisiae Induction Regimes
Recombinant membrane protein yields can be optimized in Saccharomyces cerevisiae by adjusting the induction time and temperature and/or by the addition of chemical chaperones. Here we describe a protocol for assessing the importance
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