AMPD3 抗体 (Middle Region)
Quick Overview for AMPD3 抗体 (Middle Region) (ABIN360232)
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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抗原表位
- Middle Region
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特异性
- This antibody detects AMPD3 at Center.
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交叉反应 （详细）
- Species reactivity (tested):Human and Mouse.
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纯化方法
- Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS
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免疫原
- This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the Center region of human AMPD3.
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亚型
- Ig Fraction
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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 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
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ELISA: 1/1,000. Western blot: 1/50-1/100.
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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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS with 0.09 % (W/V) Sodium Azide as preservative
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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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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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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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- AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))
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别名
- AMP Deaminase 3 / AMPD3
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背景
- AMPD3 is a member of the AMP deaminase gene family. This 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. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.Synonyms: AMP deaminase isoform E, Erythrocyte AMP deaminase
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分子量
- 88812 Da
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基因ID
- 272, 9606
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UniProt
- Q01432
抗原
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