AMPD1 抗体 (AA 230-310)
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Quick Overview for AMPD1 抗体 (AA 230-310) (ABIN7221078)
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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抗原表位
- AA 230-310
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原理
- AMPD1 Polyclonal Antibody
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特异性
- AMPD1 Polyclonal Antibody detects endogenous levels of AMPD1 protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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免疫原
- Synthesized peptide derived from the Internal region of human AMPD1 at AA range: 230-310
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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
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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说明
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Primary Antibody
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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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
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))
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别名
- AMPD1
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背景
- Rabbit Anti-AMPD1 Polyclonal Antibody,AMPD1, AMP deaminase 1, AMP deaminase isoform M, Myoadenylate deaminase,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.,AMP deaminase 1
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基因ID
- 270
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UniProt
- P23109
抗原
-
