-
- 抗原 See all ACP2 抗体
- ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This ACP2 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), ELISA
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Antigen affinity purification
- 免疫原
- Synthetic peptide of Human ACP2
- 亚型
- IgG
- Top Product
- Discover our top product ACP2 Primary Antibody
-
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 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) (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
-
- 应用备注
- ELISA:1:1000-1:2000, WB:1:200-1:1000,
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 缓冲液
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- 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,-80 °C
- 储存方法
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
-
- 抗原
- ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
- 别名
- ACP2 (ACP2 产品)
- 别名
- ACP2 antibody, Acp-2 antibody, LAP antibody, acid phosphatase 2, lysosomal antibody, acid phosphatase 2, lysosomal S homeolog antibody, ACP2 antibody, acp2 antibody, Acp2 antibody, acp2.S antibody
- 背景
-
Background: This gene encodes the beta subunit of lysosomal acid phosphatase (LAP). LAP is chemically and genetically distinct from red cell acid phosphatase. The encoded protein belongs to a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Mutations in this gene or in the related alpha subunit gene cause acid phosphatase deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
Aliases: ACP2 antibody, Lysosomal acid phosphatase antibody, LAP antibody, EC 3.1.3.2 antibody
- UniProt
- P11117
-
You are here:
