AMPD1 抗体
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- 抗原 See all AMPD1 抗体
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
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适用
- 人, 小鼠, 大鼠
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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 AMPD1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human AMPD1 (NP_001166097.1).
- 亚型
- IgG
- Top Product
- Discover our top product AMPD1 Primary Antibody
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anti-Adenosine Monophosphate Deaminase 1 (AMPD1) (AA 50-260) antibody
AMPD1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) antibodyAMPD1 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) (AA 101-200) antibodyAMPD1 适用: 小鼠, 大鼠 ELISA, IF (cc), IF (p), IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 1 (AMPD1) (AA 97-272) antibodyAMPD1 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
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- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
- 别名
- AMPD1 (AMPD1 产品)
- 别名
- ampd1 antibody, MAD antibody, MADA antibody, AI553520 antibody, Ampd-1 antibody, Ampd01 antibody, RATAMPD01 antibody, zgc:77905 antibody, adenosine monophosphate deaminase 1 antibody, N-acetyl-anhydromuranmyl-L-alanine amidase antibody, N-acetylmuramoyl-L-alanine amidase antibody, Negative regulator of beta-lactamase expression antibody, adenosine monophosphate deaminase 1 (isoform M) antibody, AMPD1 antibody, ampD1 antibody, ampd1 antibody, Ampd1 antibody
- 背景
- AMPD1,MAD,MADA,MMDD,Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.
- 分子量
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Observed_MW: 80 kDa
Calculated_MW: 89 kDa/90 kDa
- 基因ID
- 270
- UniProt
- P23109
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