Arylsulfatase B 抗体 (AA 235-266)
Quick Overview for Arylsulfatase B 抗体 (AA 235-266) (ABIN652346)
抗原
See all Arylsulfatase B (ARSB) 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 235-266
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This ARSB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 235-266 amino acids from the Central region of human ARSB.
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亚型
- Ig Fraction
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anti-Arylsulfatase B (ARSB) (Internal Region) antibody
Verified ARSB 适用: 人 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Arylsulfatase B (ARSB) (AA 81-533) antibodyARSB 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase B (ARSB) (AA 37-533) antibodyARSB 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase B (ARSB) (AA 166-265) antibodyARSB 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Arylsulfatase B (ARSB) (AA 166-265) antibodyARSB 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1A4 unconjugated
anti-Arylsulfatase B (ARSB) (AA 300-349) antibodyARSB 适用: 人, 小鼠, Cow, 犬, 豚鼠, 马, 猴, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase B (ARSB) antibodyARSB 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase B (ARSB) (AA 464-493), (C-Term) antibodyARSB 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB18353 unconjugated
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应用备注
- WB: 1:1000. WB: 1:1000
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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
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
- 4 °C,-20 °C
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储存方法
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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有效期
- 6 months
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- Arylsulfatase B (ARSB)
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别名
- ARSB
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背景
- ARSB 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.
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分子量
- 59687
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基因ID
- 411
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NCBI登录号
- NP_000037, NP_942002
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UniProt
- P15848
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途径
- Glycosaminoglycan Metabolic Process
抗原
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