DMGDH 抗体 (AA 790-870)
Our Local Distributor
北京 101111
Quick Overview for DMGDH 抗体 (AA 790-870) (ABIN7214582)
抗原
See all DMGDH 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 790-870
-
原理
- Rabbit Anti-DMGDH Polyclonal Antibody
-
特异性
- DMGDH Polyclonal Antibody detects endogenous levels of DMGDH protein.
-
纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-
免疫原
- Synthesized peptide derived from the C-terminal region of human DMGDH at AA range: 790-870
-
亚型
- IgG
-
-
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, 小鼠, 大鼠, 猴 WB, IHC 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,ELISA 1:20000,IF 1:50-200
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 1 mg/mL
-
缓冲液
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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
-
储存方法
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
-
有效期
- 12 months
-
-
- DMGDH (Dimethylglycine Dehydrogenase (DMGDH))
-
别名
- DMGDH
-
背景
- DMGDH, Dimethylglycine dehydrogenase, mitochondrial, ME2GLYDHDMGDH encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme (dimethylglycine dehydrogenase) 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
- 97kD
-
基因ID
- 29958
-
UniProt
- Q9UI17
抗原
-
