Aminomethyltransferase 抗体
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- 抗原 See all Aminomethyltransferase (AMT) 抗体
- Aminomethyltransferase (AMT)
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适用
- 人, 小鼠, 大鼠, 犬
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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 Aminomethyltransferase antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 纯化方法
- Antibody is purified by peptide affinity chromatography method.
- 免疫原
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human AMT.
- Top Product
- Discover our top product AMT Primary Antibody
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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.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- 浓度
- 1 mg/mL
- 缓冲液
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- 注意事项
- As with any antibody avoid repeat freeze-thaw cycles.
- 储存条件
- 4 °C/-20 °C
- 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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- 抗原
- Aminomethyltransferase (AMT)
- 别名
- AMT (AMT 产品)
- 别名
- F16J13.200 antibody, F16J13_200 antibody, T7P1.13 antibody, T7P1_13 antibody, wu:fc31f04 antibody, wu:fd44b12 antibody, wu:fd54h12 antibody, zgc:103483 antibody, zgc:109741 antibody, GCE antibody, GCST antibody, GCVT antibody, NKH antibody, EG434437 antibody, aminomethyltransferase antibody, Glycine cleavage T-protein family antibody, Aminomethyltransferase antibody, aminomethyltransferase L homeolog antibody, AMT antibody, AT4G12130 antibody, AT1G60990 antibody, Tb11.01.1440 antibody, Palpr_0614 antibody, Ocepr_1643 antibody, Celal_2914 antibody, Deima_1002 antibody, Deipr_1956 antibody, Bacsa_3405 antibody, Celly_0288 antibody, Weevi_0527 antibody, Fluta_3952 antibody, Marky_0785 antibody, Spico_1217 antibody, Poras_1228 antibody, Halhy_3617 antibody, amt antibody, amt.L antibody, Amt antibody
- 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.
- 分子量
- 44 kDa
- 基因ID
- 275
- NCBI登录号
- NP_000472
- UniProt
- P48728
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