Arylsulfatase A 抗体 (C-Term)
Quick Overview for Arylsulfatase A 抗体 (C-Term) (ABIN1536617)
抗原
See all Arylsulfatase A (ARSA) 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 408-439, C-Term
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纯化方法
- This antibody is purified through a protein G column, followed by dialysis against PBS.
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免疫原
- This ARSA antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 408-439 amino acids from the C-terminal region of human ARSA.
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亚型
- IgG2a
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anti-Arylsulfatase A (ARSA) (Internal Region) antibody
Verified ARSA 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA, FACS, IF 宿主: 山羊 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) antibodyARSA 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) (Internal Region) antibodyARSA 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) antibodyARSA 适用: 人, 小鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) (AA 1-507) antibodyARSA 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) (AA 1-507) antibodyARSA 适用: 人 WB, IHC (p) 宿主: 小鼠 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) (AA 210-509) antibodyARSA 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) (AA 454-482), (C-Term) antibodyARSA 适用: 人, 小鼠, 大鼠 WB, IHC, FACS, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) (AA 21-295) antibodyARSA 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Arylsulfatase A (ARSA) antibodyARSA 适用: 人, 小鼠, 大鼠 WB, FACS, IHC (p) 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:100~250
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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 monoclonal 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
- ARSA Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
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有效期
- 6 months
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- Arylsulfatase A (ARSA)
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别名
- ARSA
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背景
- The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.
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分子量
- 53588
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基因ID
- 410
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NCBI登录号
- NP_000478, NP_001078894, NP_001078895, NP_001078896, NP_001078897
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UniProt
- P15289
抗原
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