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- 抗原 See all DMGDH 抗体
- DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This DMGDH antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 交叉反应
- 人
- 纯化方法
- Affinity purification
- 免疫原
- Recombinantproteincorrespondingto Mouse DMGDH
- Top Product
- Discover our top product DMGDH Primary Antibody
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anti-Dimethylglycine Dehydrogenase (DMGDH) (AA 429-524) antibody
DMGDH 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dimethylglycine Dehydrogenase (DMGDH) (C-Term) antibodyDMGDH 适用: 人, 小鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Dimethylglycine Dehydrogenase (DMGDH) (C-Term) antibodyDMGDH 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Dimethylglycine Dehydrogenase (DMGDH) (C-Term) antibodyDMGDH 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Dimethylglycine Dehydrogenase (DMGDH) (C-Term) antibodyDMGDH 适用: 人, 猴 WB, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB (H) 1:500-1:1000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS, pH 7.4, 0.02 % sodium azide
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
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- 抗原
- DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
- 别名
- DMGDH (DMGDH 产品)
- 别名
- MGC132281 antibody, DMGDHD antibody, ME2GLYDH antibody, Me2GlyDH antibody, 1200014D15Rik antibody, AI787269 antibody, dimethylglycine dehydrogenase antibody, dimethylglycine dehydrogenase L homeolog antibody, D-amino-acid oxidase antibody, Dimethylglycine dehydrogenase antibody, glycine cleavage system protein T antibody, dimethylglycine dehydrogenase precursor antibody, DMGDH antibody, dmgdh.L antibody, dmgdh antibody, SAR11_1253 antibody, EAMY_RS27375 antibody, EAMY_RS33570 antibody, VDBG_06516 antibody, Sinme_2570 antibody, HALXA_RS03495 antibody, Dmgdh antibody
- 背景
- This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. Alternative splicing results in multiple transcript variants.
- 分子量
- 97 kDa
- 基因ID
- 74129
- NCBI登录号
- NP_083048
- UniProt
- Q9DBT9
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