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GALT 抗体

GALT 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5708385
发货至: 中国
  • 抗原 See all GALT 抗体
    GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))
    适用
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    宿主
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    克隆类型
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    多克隆
    标记
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    This GALT antibody is un-conjugated
    应用范围
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    Western Blotting (WB), ELISA
    纯化方法
    Antigen affinity purified
    免疫原
    A recombinant human partial protein corresponding to amino acids Q188-A379 was used as the immunogen for the GALT antibody.
    亚型
    IgG
    Top Product
    Discover our top product GALT Primary Antibody
  • 应用备注
    Optimal dilution of the GALT antibody should be determined by the researcher.\. Western Blot: 0.5-1 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 GALT 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
    GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))
    别名
    GALT / Galactose-1-phosphate uridyl transferase (GALT 产品)
    别名
    GALT antibody, AW553376 antibody, CG9232 antibody, Dmel\\CG9232 antibody, dGALT antibody, galactose-1-phosphate uridylyltransferase antibody, galactose-1-phosphate uridylyltransferase, GalT antibody, probable galactose-1-phosphate uridylyltransferase galtb [second part] antibody, UDP-glucose--galactose-1-phosphate uridylyltransferase antibody, GalT galactose-1-phosphate uridylyltransferase antibody, galactose-1-phosphate uridyl transferase antibody, Galactose-1-phosphate uridylyltransferase antibody, galactose-1-phosphate uridylyltransferase S homeolog antibody, GALT antibody, galT antibody, Galt antibody, CNM00620 antibody, Mrub_2813 antibody, Mesil_2395 antibody, Trad_0989 antibody, Igag_1846 antibody, VDIS_RS10425 antibody, Intca_2810 antibody, Marky_2157 antibody, Selsp_1876 antibody, Trebr_2368 antibody, Halhy_5538 antibody, Theth_1357 antibody, galt.S antibody
    背景
    Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene.
    UniProt
    P07902
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