Arylsulfatase B 抗体 (C-Term)
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- 抗原 See all Arylsulfatase B (ARSB) 抗体
- Arylsulfatase B (ARSB)
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抗原表位
- AA 460-510, C-Term
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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 Arylsulfatase B antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
- 特异性
- ARSB antibody is human, mouse and rat reactive. At least two isoforms of ARSB are known to exist, this antibody only recognizes the longest isoform.
- 纯化方法
- ARSB Antibody is affinity chromatography purified via peptide column.
- 免疫原
- ARSB antibody was raised against a 16 amino acid peptide near the carboxy terminus of human ARSB. The immunogen is located within amino acids 460 - 510 of ARSB .
- 亚型
- IgG
- Top Product
- Discover our top product ARSB Primary Antibody
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- 应用备注
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ARSB antibody can be used for detection of ARSB by Western blot at 1 - 2 μ,g/mL.
Antibody validated: Western Blot in mouse samples, Immunohistochemistry in human samples and Immunofluorescence in human samples. All other applications and species not yet tested. - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- ARSB Antibody is supplied in PBS containing 0.02 % sodium azide.
- 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,4 °C
- 储存方法
- ARSB antibody can be stored at 4°C for three months and -20°C, stable for up to one year.
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- 抗原
- Arylsulfatase B (ARSB)
- 别名
- ARSB (ARSB 产品)
- 别名
- ASB antibody, G4S antibody, MPS6 antibody, 1110007C02Rik antibody, AI480648 antibody, As-1 antibody, As-1r antibody, As-1s antibody, As-1t antibody, As1 antibody, As1-r antibody, As1-s antibody, As1-t antibody, Asr-1 antibody, Ast-1 antibody, ARSB antibody, arylsulfatase B antibody, arylsulfatase antibody, arylsulfatase b antibody, ARSB antibody, Arsb antibody, RB348 antibody, LOC5566067 antibody, CpipJ_CPIJ011047 antibody, VDBG_03275 antibody, arsb antibody, LOC5579667 antibody
- 背景
- Aryl sulfatase B (ARSB) forms a homodimer that hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate (1). ARSB localizes to the lysozyme as well as to the extracellular matrix (2). Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B (3), and can be treated with exogenous ARSB (4).
- 分子量
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Predicted: 59 kDa
Observed: 57kDa - 基因ID
- 411
- NCBI登录号
- NP_000037
- UniProt
- P15848
- 途径
- Glycosaminoglycan Metabolic Process
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