Recombinant-Human-Mitochondria
l-ornithine-transporter-2SLC25A2Mitochondrial ornithine transporter 2 Alternative name(s): Solute carrier family 25 member 2- ￥11452
- CUSABIO
- CN
- CSB-CF883620HU
- 2025年07月12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 Human SLC25A2 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)
Mitochondrial ornithine transporter 2 Alternative name(s): Solute carrier family 25 member 2Editorial/Sponsord
EditorialUniprot ID
Q9BXI2Gene Names
SLC25A2Organism
HumanAASequence
MKSGPGIQAAIDLTAGAAGGTACVLTGQPFDTIKVKMQTFPDLYKGLTDCFLKTYAQVGL RGFYKGTGPALMAYVAENSVLFMCYGFCQQFVRKVAGMDKQAKLSDLQTAAAGSFASAFA ALALCPTELVKCRLQTMYEMEMSGKIAKSHNTIWSVVKGILKKDGPLGFYHGLSSTLLQE VPGYFFFFGGYELSRSFFASGRSKDELGPVHLMLSGGVAGICLWLVVFPVDCIKSRIQVL SMYGKQAGFIGTLLSVVRNEGIVALYSGLKATMIRAIPANGALFVAYEYSRKMMMKQLEA YExpression Region
1-301aaSequence Info
Full lengthSource
in vitro E.coliSource Notice
Mammalian cell expression systems and other species are available. Please inquire.Tag Info
InquireMW
InquireList Price
1636Purity
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
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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
Purification Strategy for Recombinant Formsof the Human Mitochondrial DNA Helicase
In this chapter, we present a streamlined purification for the production of near-homogeneous and high yield recombinant forms of the human mitochondrial DNA helicase. Minimizing the number of steps and the time elapsed for purification
Animal Models of Hereditary Hyperammonemias
superscripts. Enzymes No. 1 and 2 of the urea cycle are mitochondrial, whereas enzymes 3–5 are located in the cytosol. Primary urea cycle disorders caused by mutations related to each of these enzymes are known in various human patients.
三句话读懂一篇 CNS：每天要走多少步，才能降低死亡风险？这种蔬菜的完整基因组终被破译
代谢病，目前无有效疗法。 2022 年 3 月 3 日，温州医科大学检验医学院 / 杭州医学院吕建新教授团队在 Science Translational Medicine 杂志发表了研究论文 SERAC1 is a component of the mitochondrial serine transporter complex required for the maintenance of mitochondrial DNA。 该研究通过 CRISPR/Cas9 基因编辑技术构建了一个全身
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