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- 抗原 See all AMPD3 抗体
- AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))
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适用
- 人
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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 AMPD3 antibody is un-conjugated
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应用范围
- Immunofluorescence (IF)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human AMPD3 (NP_000471.1).
- 亚型
- IgG
- Top Product
- Discover our top product AMPD3 Primary Antibody
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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) antibodyAMPD3 适用: 人 IF, ICC, FACS, IHC (p) 宿主: 小鼠 Monoclonal AMPD3-901 unconjugated
anti-Adenosine Monophosphate Deaminase 3 (AMPD3) (AA 541-776) antibodyAMPD3 适用: 人 WB, IHC, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))
- 别名
- AMPD3 (AMPD3 产品)
- 别名
- ampd3 antibody, fi25h10 antibody, wu:fi25h10 antibody, zgc:55390 antibody, MGC108215 antibody, adenosine monophosphate deaminase 3 antibody, adenosine monophosphate deaminase 3b antibody, AMP deaminase 3 antibody, AMPD3 antibody, ampd3b antibody, PTRG_08116 antibody, ampd3 antibody, Ampd3 antibody
- 背景
- This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described.
- 基因ID
- 272
- UniProt
- Q01432
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