AMPD1 抗体
Quick Overview for AMPD1 抗体 (ABIN7384200)
抗原
See all AMPD1 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein of human AMPD1 (NP_001166097.1).
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亚型
- IgG
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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
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限制
- 仅限研究用
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浓度
- 1 mg/mL
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缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
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别名
- AMPD1
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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.
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分子量
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Observed_MW: 80 kDa
Calculated_MW: 89 kDa/90 kDa
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基因ID
- 270
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UniProt
- P23109
抗原
-
