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GATM rabbit pAb
商品货号: PLA019948
适 应 性: 人,小鼠,大鼠
WB
¥600元
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MSDS
说明书
商品描述
  • 基因名称: GATM AGAT
  • 蛋白名称: GATM
  • Human_gene_id: 2628
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2628
  • Human_swiss_prot_no: P50440
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P50440/entry
  • Mouse_gene_id: 67092
  • Mouse_gene_link: https://www.uniprot.org/uniprot/67092
  • Mouse_swiss_prot_no: Q9D964
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9D964
  • Rat_gene_id: 81660
  • Rat_gene_link: https://www.uniprot.org/uniprot/81660
  • Rat_swiss_prot_no: P50442
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P50442
  • 特异性: This antibody detects endogenous levels of GATM at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 47kD
  • 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.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 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.
  • 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.
  • 科研货号: PLA019948
GATM rabbit pAb
Catalog No PLA019948
Product information
  • 基因名称: GATM AGAT
  • 蛋白名称: GATM
  • Human_gene_id: 2628
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2628
  • Human_swiss_prot_no: P50440
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/P50440/entry
  • Mouse_gene_id: 67092
  • Mouse_gene_link: https://www.uniprot.org/uniprot/67092
  • Mouse_swiss_prot_no: Q9D964
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9D964
  • Rat_gene_id: 81660
  • Rat_gene_link: https://www.uniprot.org/uniprot/81660
  • Rat_swiss_prot_no: P50442
  • Rat_swiss_link: https://www.uniprot.org/uniprotkb/P50442
  • 特异性: This antibody detects endogenous levels of GATM at Human/Mouse/Rat
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 47kD
  • 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.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 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.
  • 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.
  • 科研货号: PLA019948
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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