AMPD3 抗体 (AbBy Fluor® 680)
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北京 101111
Quick Overview for AMPD3 抗体 (AbBy Fluor® 680) (ABIN4996426)
抗原
See all AMPD3 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human AMPD3
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亚型
- IgG
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anti-Adenosine Monophosphate Deaminase 3 (AMPD3) antibody
AMPD3 适用: 人 IHC, StM 宿主: 小鼠 Monoclonal AMPD3-901 unconjugated
anti-Adenosine Monophosphate Deaminase 3 (AMPD3) (AA 1-260) antibodyAMPD3 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 3 (AMPD3) (AA 325-356) antibodyAMPD3 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB17671 unconjugated
anti-Adenosine Monophosphate Deaminase 3 (AMPD3) (AA 541-776) antibodyAMPD3 适用: 人 WB, IHC, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 3 (AMPD3) antibodyAMPD3 适用: 人 IF 宿主: 兔 Polyclonal unconjugated
anti-Adenosine Monophosphate Deaminase 3 (AMPD3) antibodyAMPD3 适用: 人 IF, ICC, FACS, IHC (p) 宿主: 小鼠 Monoclonal AMPD3-901 unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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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 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))
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别名
- AMPD3
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背景
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Synonyms: Adenosine monophosphate deaminase isoform E, Adenosine monophosphate deaminase 3, AMP aminohydrolase, AMP deaminase 3, AMP deaminase isoform E, Ampd3, AMPD3_HUMAN, Erythrocyte AMP deaminase, Erythrocyte specic AMP deaminase, Erythrocyte type AMP deaminase, Myoadenylate deaminase.
Background: AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE), also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50 % increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.
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基因ID
- 272
抗原
-
