AMT Antibody
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货号:CSB-PA001684LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) AMT Polyclonal antibody
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Uniprot No.:P48728
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基因名:AMT
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别名:Aminomethyltransferase (glycine cleavage system protein T) antibody; Aminomethyltransferase antibody; AMT antibody; GCE antibody; GCST antibody; GCST_HUMAN antibody; GCVT antibody; Glycine cleavage system T protein antibody; mitochondrial antibody; NKH antibody
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宿主:Rabbit
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反应种属:Human, Mouse
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免疫原:Recombinant Human Aminomethyltransferase, mitochondrial protein (180-260AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,AMT Antibody (CSB-PA001684LA01HU),的标记方式是Non-conjugated。对于AMT 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, WB
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 -
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:The glycine cleavage system catalyzes the degradation of glycine.
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基因功能参考文献:
- The position and frequency of the breakpoint for CNVs correlated with intron size and presence of Alu elements. Missense mutations, most often recurring, were the most common type of disease-causing mutation in AMT PMID: 27362913
- Data indicate no mutation was found in glycine cleavage system protein-H (GCSH) and suggest that mutations in both glycine decarboxylase (GLDC) and aminomethyltransferase (AMT) are the main cause of glycine encephalopathy in Malaysian population. PMID: 25231368
- Two unique non-synonymous changes were identified in the AMT gene in patients with neural tube defects. PMID: 22171071
- x-ray crystallographic structure of human T-protein of glycine cleavage system PMID: 16051266
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相关疾病:Non-ketotic hyperglycinemia (NKH)
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亚细胞定位:Mitochondrion.
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蛋白家族:GcvT family
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数据库链接:
HGNC: 473
OMIM: 238310
KEGG: hsa:275
STRING: 9606.ENSP00000273588
UniGene: Hs.102
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