Aminomethyltransferase 抗体 (N-Term)
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Quick Overview for Aminomethyltransferase 抗体 (N-Term) (ABIN631086)
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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抗原表位
- N-Term
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特异性
- AMT antibody was raised against the N terminal of AMT
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纯化方法
- Affinity purified
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免疫原
- AMT antibody was raised using the N terminal of AMT corresponding to a region with amino acids QRAVSVVARLGFRLQAFPPALCRPLSCAQEVLRRTPLYDFHLAHGGKMVA
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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) (AA 107-386) antibodyAMT 适用: 人 WB, IHC, IF 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 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
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应用备注
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. -
说明
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AMT Blocking Peptide, (ABIN5612052), is also available for use as a blocking control in assays to test for specificity of this AMT antibody
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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
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of AMT antibody in PBS
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浓度
- Lot specific
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缓冲液
- PBS
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注意事项
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. -
储存条件
- 4 °C/-20 °C
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储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store 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.
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分子量
- 44 kDa (MW of target protein)
抗原
-
