Mut Antibody
产品详情
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产品名称:Rabbit anti-Mus musculus (Mouse) Mut Polyclonal antibody
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Uniprot No.:P16332
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基因名:Mut
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别名:Mmut antibody; Mut antibody; Methylmalonyl-CoA mutase antibody; mitochondrial antibody; MCM antibody; EC 5.4.99.2 antibody; Methylmalonyl-CoA isomerase antibody
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宿主:Rabbit
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反应种属:Mouse
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免疫原:Recombinant Mouse Methylmalonyl-CoA mutase, mitochondrial protein (31-748AA)
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免疫原种属:Mus musculus (Mouse)
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标记方式:Non-conjugated
本页面中的产品,Mut Antibody (CSB-PA015243YA01MO),的标记方式是Non-conjugated。对于Mut Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA
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Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:Catalyzes the reversible isomerization of methylmalonyl-CoA (MMCoA) (generated from branched-chain amino acid metabolism and degradation of dietary odd chain fatty acids and cholesterol) to succinyl-CoA (3-carboxypropionyl-CoA), a key intermediate of the tricarboxylic acid cycle.
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基因功能参考文献:
- On a high protein diet, mutant mice display disease exacerbation, including elevated blood ammonia, and catastrophic weight loss, which, in Mut(ki/ki) mice, is rescued by hydroxocobalamin treatment. This study expands knowledge of MMAuria, introduces the discovery of new biomarkers, and constitutes the first in vivo proof of principle of cobalamin treatment in mut-type MMAuria. PMID: 27519416
- The mouse methylmalonic aciduria- related genes, Mmaa, Mmab, and Mut may have specialized functions depending on the tissue or cell type. PMID: 23022071
- Includes the study of an upstream ORF in this gene, and shows that it functions to reduce protein levels by ~61%. PMID: 19372376
- methylmalonyl-CoA mutase has a role in methylmalonic aciduria and early neonatal lethality PMID: 14555645
- Mitochondrial dysfunction in Mut is reported. PMID: 19088183
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亚细胞定位:Mitochondrion matrix. Mitochondrion. Cytoplasm.
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蛋白家族:Methylmalonyl-CoA mutase family
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数据库链接:
KEGG: mmu:17850
STRING: 10090.ENSMUSP00000130941
UniGene: Mm.259884
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