ACP2 抗体 (N-Term) (Fluoro550)
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北京 101111
Quick Overview for ACP2 抗体 (N-Term) (Fluoro550) (ABIN7965531)
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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抗原表位
- N-Term
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原理
- Anti-ACP2 Antibody Fluoro550 Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- A synthetic peptide corresponding to a sequence at the N-terminus of human ACP2, which shares 100% and 96.4% amino acid (aa) sequence identity with mouse and rat ACP2, respectively.
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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) (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) antibodyACP2 适用: 人 WB, IF, IHC (p), EIA 宿主: 小鼠 Monoclonal M1-4A12 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
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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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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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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- ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
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别名
- ACP2
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背景
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Background: 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.
Gene Full Name: acid phosphatase 2, lysosomal
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基因ID
- 53
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UniProt
- P11117
抗原
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