Arylsulfatase B 抗体
Our Local Distributor
北京 101111
Quick Overview for Arylsulfatase B 抗体 (ABIN7880005)
抗原
See all Arylsulfatase B (ARSB) 抗体适用
宿主
克隆类型
标记
应用范围
-
-
原理
- Arylsulfatase B Antibody / Arsb
-
序列
- KTLWLFDINQ DPEERHD
-
纯化方法
- Affinity purified
-
免疫原
- Amino acids KTLWLFDINQDPEERHD from the mouse protein were used as the immunogen for the Arylsulfatase B antibody.
-
亚型
- IgG
-
-
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 464-493), (C-Term) antibodyARSB 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB18353 unconjugated
anti-Arylsulfatase B (ARSB) (AA 235-266) antibodyARSB 适用: 人 WB 宿主: 兔 Polyclonal RB18352 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 166-265) antibodyARSB 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1A4 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 37-533) antibodyARSB 适用: 人 WB, ELISA 宿主: 兔 Polyclonal 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
-
-
应用备注
- Optimal dilution of the Arylsulfatase B antibody should be determined by the researcher.
-
限制
- 仅限研究用
-
-
-
状态
- Lyophilized
-
缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
-
储存条件
- 4 °C,-20 °C
-
储存方法
- After reconstitution, the Arylsulfatase B antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
-
-
- Arylsulfatase B (ARSB)
-
别名
- Arylsulfatase B
-
背景
- 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 targeted 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
-
UniProt
- P50429
-
途径
- Glycosaminoglycan Metabolic Process
抗原
-
