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- 抗原 See all AMPD1 抗体
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
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抗原表位
- N-Term
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适用
- 人, 小鼠, 大鼠, Cow, 犬, 马, 兔, 豚鼠
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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)
- 序列
- QKSFQRFPKT PSKYLRNIDG EAWVANESFY PVFTPPVKKG EDPFRTDNLP
- 预测反应
- Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%
- 产品特性
- This is a rabbit polyclonal antibody against AMPD1. It was validated on Western Blot.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the N-terminal region of Human AMPD1
- 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
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- 抗原
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
- 别名
- AMPD1 (AMPD1 产品)
- 背景
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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.
Alias Symbols: AMPD1,
Protein Interaction Partner: Htt, CAND1, COPS5, CUL1, CUL3, MYH2,
Protein Size: 776 - 基因ID
- 270
- NCBI登录号
- NP_001166097
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