AMPD1 抗体 (AA 500-550)
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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
- AA 500-550
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适用
- 人, 小鼠, 大鼠, Cow, 猴, Chimpanzee, 斑马鱼
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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), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 特异性
- This antibody recognizes AMPD1.
- 交叉反应 （详细）
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Species reactivity (expected):Bovine, Chimpanzee, Monkey, Mouse, Rat and Zebrafish.
Species reactivity (tested):Human. - 纯化方法
- Immunoaffinity Chromatography.
- 免疫原
- Synthetic peptide corresponding to a portion of the amino acids 500-550 of Human AMPD1.
- 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
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Immunohistochemistry on Paraffin Sections: 5-10 μg/mL. Western Blot: 0.5-2.0 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - 限制
- 仅限研究用
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- 浓度
- 0.5 mg/mL
- 缓冲液
- PBS containing 0.05 % Sodium Azide as preservative and 0.2 % Gelatin as stabilizer.
- 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.
- 注意事项
- Avoid repeated freezing and thawing.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
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- 抗原
- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
- 别名
- AMP Deaminase 1 / AMPD1 (AMPD1 产品)
- 背景
- AMP deaminase (AMPD) is an allosteric enzyme that plays a critical role in energy metabolism. There are three functional isoforms of AMPD. AMPD1 is the skeletal muscle-specific isoform M located in type II muscle fibers, neuromuscular junctions and in capillaries. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type (AMPDDM). AMPDDM is a metabolic disorder resulting in exercise-related myopathy. It is characterized by exercise-induced muscle aches, cramps, and early fatigue.Synonyms: AMP deaminase isoform M, Myoadenylate deaminase
- 分子量
- 87 kDa.
- 基因ID
- 270
- NCBI登录号
- NP_000027
- UniProt
- P23109
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