ACPL2 抗体
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- 抗原 See all ACPL2 抗体
- ACPL2 (Acid Phosphatase-Like 2 (ACPL2))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This ACPL2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ACPL2
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- ACPL2 (Acid Phosphatase-Like 2 (ACPL2))
- 别名
- ACPL2 (ACPL2 产品)
- 别名
- ACPL2 antibody, ESP49.9 antibody, MGC146822 antibody, wu:fj34f09 antibody, zgc:92652 antibody, 9430094M07Rik antibody, BB177120 antibody, C130099A20Rik antibody, 2-phosphoxylose phosphatase 1 antibody, acid phosphatase-like 2 antibody, PXYLP1 antibody, pxylp1 antibody, acpl2 antibody, LOC100546815 antibody, Pxylp1 antibody
- 背景
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Synonyms: acid phosphatase-like 2, Acid phosphatase-like protein 2, acpl2, ACPL2_HUMAN, EC=3.1.3.2.
Background: ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
- 基因ID
- 92370
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