Recombinant-Saccharomyces-cere
visiae-Putative-uncharacterized-protein-VPS65VPS65Putative uncharacterized protein VPS65- ￥9702
- CUSABIO
- CN
- CSB-CF517542SVG
- 2025年07月11日
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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 VPS65 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 VPS65Editorial/Sponsord
EditorialUniprot ID
O13554Gene Names
VPS65Organism
Saccharomyces cerevisiaeAASequence
MRHCIIFIVCISIVEIRTVHIEFIKEIVVIFRIVDHFSPFMLPCLLSHCKDGDTIIFVCQ SVMKVRNISLWNKLVLVRHCVLLCAFLLSFFNVLHSIISICRIFExpression Region
1-104aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1386Purity
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
Genetic approaches have revealed more than 50 genes involved in the delivery of soluble zymogens like carboxypeptidase Y (CPY) to the lysosome-like vacuole in Saccharomyces cerevisiae . At least 20 of these genes function in transport
复发，无法根治，给患者带来了极大的心理压力，严重影响患者的生存质量。角质形成细胞中丝苏氨酸蛋白磷酸酶 -6（PP6）的表达失衡是银屑病炎症的主要原因，平衡角质形成细胞中 PP6 的表达有望成为治疗银屑病的全新策略。 2022 年 12 月 19 日上海交通大学医学院的王宏林教授和他的团队在nature communications上发表了题为「Targeting the transcription factor Hes1 by L-menthol restores protein
Chromatin Immunoprecipitation (ChIP)
of SIR protein interactions in Saccharomyces cerevisiae . Soon thereafter, Rundlett et al. (1998) used ChIP with a PCR detection step to analyze histone modifications at specific loci. At approximately the same time, the ChIP procedure was adapted
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