Arylsulfatase B 抗体
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- 抗原 See all Arylsulfatase B (ARSB) 抗体
- Arylsulfatase B (ARSB)
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适用
- 人
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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)
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
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Rabbit polyclonal antibody to ARSB (arylsulfatase B)
ARSB antibody [N3C3] - 纯化方法
- Affinity purified by Protein A.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human ARSB. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product ARSB Primary Antibody
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- 应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
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Positive Control: ARSB transfected 293T cell , HeLa , HepG2 , mouse placenta , rat testis
Validation: Overexpression
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 6.11 mg/mL
- 缓冲液
- 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): 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
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- Arylsulfatase B (ARSB)
- 别名
- arylsulfatase B (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
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Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
Cellular Localization: Lysosome - 分子量
- 60 kDa
- 基因ID
- 411
- UniProt
- P15848
- 途径
- Glycosaminoglycan Metabolic Process
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