ACP2 抗体
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北京 101111
Quick Overview for ACP2 抗体 (ABIN7879861)
抗原
See all ACP2 抗体适用
宿主
克隆类型
标记
应用范围
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原理
- ACP2 Antibody / Lysosomal Acid Phosphatase
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序列
- RSLRFVTLLY RHGDRSPVKT YPKDPYQE
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纯化方法
- Antigen affinity purified
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免疫原
- Amino acids RSLRFVTLLYRHGDRSPVKTYPKDPYQE were used as the immunogen for the ACP2 antibody.
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亚型
- IgG
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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) antibodyACP2 适用: 人 WB, IF, IHC (p), EIA 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) (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 80-129) antibodyACP2 适用: 人, 大鼠, 小鼠, 犬, Cow, 豚鼠, 兔 WB 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) antibodyACP2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Acid Phosphatase 2, Lysosomal (ACP2) (Middle Region) antibodyACP2 适用: 人, 大鼠, 小鼠, 犬, Cow, 豚鼠, 马, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the ACP2 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the ACP2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
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别名
- ACP2
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背景
- Lysosomal acid phosphatase is an enzyme that in humans is encoded by the ACP2 gene. The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism.
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UniProt
- P11117
抗原
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