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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 Human SCD5 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)
Stearoyl-CoA desaturase 5 EC= 1.14.19.1 Alternative name(s): Acyl-CoA-desaturase 4 HSCD5 Stearoyl-CoA 9-desaturaseEditorial/Sponsord
EditorialUniprot ID
Q86SK9Gene Names
SCD5Organism
HumanAASequence
MPGPATDAGKIPFCDAKEEIRAGLESSEGGGGPERPGARGQRQNIVWRNVVLMSLLHLGA VYSLVLIPKAKPLTLLWAYFCFLLAALGVTAGAHRLWSHRSYRAKLPLRIFLAVANSMAF QNDIFEWSRDHRAHHKYSETDADPHNARRGFFFSHIGWLFVRKHRDVIEKGRKLDVTDLL ADPVVRIQRKYYKISVVLMCFVVPTLVPWYIWGESLWNSYFLASILRYTISLNISWLVNS AAHMYGNRPYDKHISPRQNPLVALGAIGEGFHNYHHTFPFDYSASEFGLNFNPTTWFIDF MCWLGLATDRKRATKPMIEARKARTGDSSAExpression Region
1-330aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1674Purity
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
【思路解读】一篇 10 分 SCI 文章,教你入手「铁死亡」的国自然课题设计思路
死亡」 SREBP1 作为一种转录因子,可以调控多个脂质合成相关基因,如 ACLY、ACACA、FASN 和 SCD。 在带有 PI3K-AKT-mTOR 通路突变的受试细胞系中,SREBF1 敲除比其他靶标更显著地降低了硬脂酰 CoA 去饱和酶-1(Stearoyl-CoA desaturase-1,SCD1)的表达。 这一结果和最近报道的 SCD1 抗「铁死亡」功能共同提示了研究者:SCD1 是否是介导「铁死亡」抗性的 SREBP1 主要下游靶标。 研究发现 SCD1 抑制剂 CAY10566 使癌
Overview of the Measurement of Lipids and Lipoproteins in Mice
., Gibson, W.T., Fievet, C., Vance, J.E., Staels, B., and Hayden, M.R. 2008. Absence of stearoyl‐CoA desaturase‐1 ameliorates features of the metabolic syndrome in LDLR‐deficient mice. J. Lipid Res. 49:217‐229.
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