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GATM Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT6448
产品名称
GATM Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
GATM AGAT
蛋白名称
GATM
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
2628
Human Gene Link
https://www.uniprot.org/uniprot/2628
Human Swissprot No.
P50440
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P50440/entry
Mouse Gene ID
67092
Mouse Gene Link
https://www.uniprot.org/uniprot/67092
Mouse Swissprot No.
Q9D964
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q9D964
Rat Gene ID
81660
Rat Gene Link
https://www.uniprot.org/uniprot/81660
Rat Swissprot No.
P50442
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/P50442
免疫原
Synthesized peptide derived from human GATM AA range: 223-273
特异性
This antibody detects endogenous levels of GATM at Human/Mouse/Rat
稀释度
WB 1:500-2000
参考分子量
47kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by mental retardation, language impairment, and behavioral disorders. [provided by RefSeq, Jul 2008],
组织表达
Expressed in brain, heart, kidney, liver, lung, salivary gland and skeletal muscle tissue, with the highest expression in kidney. Biallelically expressed in placenta and fetal tissues.
细胞定位
[Isoform 1]: Mitochondrion inner membrane; Peripheral membrane protein; Intermembrane side. Probably attached to the outer side of the inner membrane.; [Isoform 2]: Cytoplasm.
功能
catalytic activity:L-arginine + glycine = L-ornithine + guanidinoacetate.,disease:Defects in GATM are the cause of L-arginine:glycine amidinotransferase deficiency (AGAT deficiency) [MIM:602360]. AGAT deficiency is a defect in creatine metabolism leading to mental retardation.,domain:One chain folds into a compact single domain composed of repeating units, five beta-beta-alpha-beta modules, which surround the central active site.,pathway:Amine and polyamine biosynthesis; creatine biosynthesis; creatine from L-arginine and glycine: step 1/2.,similarity:Belongs to the amidinotransferase family.,subcellular location:The mitochondrial form is found in the intermembrane space probably attached to the outer side of the inner membrane.,subunit:Homodimer. There is an equilibrium between the monomeric and dimeric forms, shifted towards the side of the monomer.,tissue specificity:Kidney.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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