Aminomethyltransferase 抗体
Quick Overview for Aminomethyltransferase 抗体 (ABIN2459732)
抗原
See all Aminomethyltransferase (AMT) 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Antibody is purified by peptide affinity chromatography method.
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免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human AMT.
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anti-Aminomethyltransferase (AMT) (AA 1-289) antibody
AMT 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) antibodyAMT 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) (AA 107-386) antibodyAMT 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) (AA 1-289) antibodyAMT 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) (AA 19-45), (N-Term) antibodyAMT 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB19704 unconjugated
anti-Aminomethyltransferase (AMT) antibodyAMT 适用: 人 WB, IHC, FACS 宿主: 兔 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) (AA 180-260) antibodyAMT 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) (N-Term) antibodyAMT 适用: 人, 小鼠, 大鼠, 犬, Cow, 豚鼠, 马, 兔, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Aminomethyltransferase (AMT) (N-Term) antibodyAMT 适用: 人, 小鼠, 大鼠, 犬 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- AMT antibody can be used for detection of AMT by ELISA at 1:12500. AMT antibody can be used for detection of AMT by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
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浓度
- 1 mg/mL
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缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
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注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
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储存条件
- 4 °C/-20 °C
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储存方法
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store AMT antibody at -20 °C.
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- Aminomethyltransferase (AMT)
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别名
- AMT
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背景
- The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). Glycine encephalopathy (GCE) may be due to a defect in any one of these enzymes.The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase, MIM 238300), H protein (a lipoic acid-containing protein, MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase, MIM 238331). Glycine encephalopathy (GCE, MIM 605899) may be due to a defect in any one of these enzymes.
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分子量
- 44 kDa
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基因ID
- 275
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NCBI登录号
- NP_000472
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UniProt
- P48728
抗原
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