ACP2 抗体
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- 抗原 See all ACP2 抗体
- ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This ACP2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
- 特异性
- This antibody reacts to ACP2 / Acid Phosphatase 2.
- 纯化方法
- Affinity chromatography on Protein A
- 免疫原
- ACP2 antibody was raised against recombinant protein
- 克隆位点
- M1-4A12
- 亚型
- IgG2b
- Top Product
- Discover our top product ACP2 Primary Antibody
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anti-Acid Phosphatase 2, Lysosomal (ACP2) (AA 1-423) antibody
ACP2 适用: 人 WB, ELISA, IF, IHC (p), RNAi 宿主: 小鼠 Monoclonal M1-4A12 unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) (AA 80-129) antibodyACP2 适用: 人, 大鼠, 小鼠, 犬, 兔, Cow, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) (AA 1-424) antibodyACP2 适用: 人 WB, ELISA, IHC, IF, IHC (p) 宿主: 小鼠 Monoclonal M1-4A12 unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) (AA 144-193) antibodyACP2 适用: 人, 大鼠, 小鼠, 犬, 马, Bat, Hamster WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) antibodyACP2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) (AA 1-423) antibodyACP2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) (Middle Region) antibodyACP2 适用: 人, 大鼠, 小鼠, 犬, 兔, Cow, 豚鼠, 马 WB, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- Optimal working dilution should be determined by the investigator.
- 限制
- 仅限研究用
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- 浓度
- 0,41 mg/mL
- 缓冲液
- PBS, pH 7.2
- 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
- ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
- 别名
- ACP2 / LAP (ACP2 产品)
- 背景
- Lysosomal acid phosphatase is comprised of two subunits, alpha and beta, and is chemically and genetically distinct from red cell acid phosphatase. Lysosomal acid phosphatase 2 is a member of a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Acid phosphatase deficiency is caused by mutations in the ACP2 (beta subunit) and ACP3 (alpha subunit) genes.Synonyms: Lysosomal acid phosphatase
- 基因ID
- 53
- NCBI登录号
- NP_001601
- UniProt
- P11117
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