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GALNS 抗体

GALNS 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5708456
发货至: 中国
  • 抗原 See all GALNS 抗体
    GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))
    适用
    人, 小鼠, 大鼠
    宿主
    • 55
    • 2
    • 1
    克隆类型
    • 58
    多克隆
    标记
    • 22
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    • 1
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    This GALNS antibody is un-conjugated
    应用范围
    • 44
    • 25
    • 19
    • 16
    • 13
    • 13
    • 13
    • 10
    • 8
    • 3
    • 2
    • 1
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    Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    Antigen affinity purified
    免疫原
    A recombinant human partial protein corresponding to amino acids Y181-N289 was used as the immunogen for the GALNS antibody.
    亚型
    IgG
    Top Product
    Discover our top product GALNS Primary Antibody
  • 应用备注
    Optimal dilution of the GALNS antibody should be determined by the researcher.\. Western Blot: 0.5-1 μg/mL,IHC (FFPE): 1-2 μg/mL,Direct ELISA: 0.1-0.5 μg/mL
    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 GALNS 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
    GALNS (Galactosamine (N-Acetyl)-6-Sulfate Sulfatase (GALNS))
    别名
    GALNS (GALNS 产品)
    别名
    GALNAC6S antibody, GAS antibody, GalN6S antibody, MPS4A antibody, mFLJ00319 antibody, galns antibody, zgc:158385 antibody, galactosamine (N-acetyl)-6-sulfatase antibody, galactosamine (N-acetyl)-6-sulfate sulfatase antibody, N-acetylgalactosamine-6-sulfatase antibody, galactosamine (N-acetyl)-6-sulfatase L homeolog antibody, GALNS antibody, Galns antibody, Celly_0425 antibody, galns.L antibody, galns antibody
    背景
    N-acetylgalactosamine-6-sulfatase is an enzyme that, in humans, is encoded by the GALNS gene. This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder.
    UniProt
    P34059
    途径
    Glycosaminoglycan Metabolic Process
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