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Arylsulfatase A 抗体

ARSA 适用: 人, 小鼠, 大鼠 WB, IHC (p), FACS 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN4950226
发货至: 中国
  • 抗原 See all Arylsulfatase A (ARSA) 抗体
    Arylsulfatase A (ARSA)
    适用
    • 56
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    人, 小鼠, 大鼠
    宿主
    • 54
    • 16
    • 1
    克隆类型
    • 57
    • 14
    多克隆
    标记
    • 35
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    This Arylsulfatase A antibody is un-conjugated
    应用范围
    • 54
    • 22
    • 14
    • 13
    • 13
    • 9
    • 7
    • 7
    • 6
    • 4
    • 4
    • 1
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    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
    纯化方法
    Antigen affinity
    免疫原
    Amino acids QALKQLQLLKAQLDAAVTFGPSQVARGED of human ARSA were used as the immunogen for the ARSA antibody.
    亚型
    IgG
    Top Product
    Discover our top product ARSA Primary Antibody
  • 应用备注
    Optimal dilution of the ARSA antibody should be determined by the researcher.\. Western blot: 0.1-0.5 μg/mL,IHC (Paraffin): 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells
    限制
    仅限研究用
  • 缓冲液
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    储存条件
    -20 °C
    储存方法
    After reconstitution, the ARSA antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原
    Arylsulfatase A (ARSA)
    别名
    ARSA (ARSA 产品)
    别名
    ARSA antibody, zgc:101575 antibody, arsa antibody, AS-A antibody, ASA antibody, AW212749 antibody, As-2 antibody, As2 antibody, TISP73 antibody, MLD antibody, mld antibody, arylsulfatase A antibody, arylsulfatase antibody, arylsulfatase A, gene 1 S homeolog antibody, ARSA antibody, arsa antibody, arsA antibody, RB6599 antibody, Arsa antibody, arsa.1.S antibody
    背景
    Arylsulfatase A (ARSA) is an enzyme that breaks down sulfatides, namely cerebroside 3-sulfate intocerebroside and sulfate. In humans, arylsulfatase A is encoded by the ARSA gene. ARSA is mapped to 22q13.33. 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.
    UniProt
    P15289
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