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GALT 抗体 (AA 251-350)

This anti-GALT antibody is a 兔 多克隆 antibody detecting GALT in WB, ELISA, IHC (p), IF (cc), IF (p) 和 IHC (fro). Suitable for 大鼠 和 小鼠.
产品编号 ABIN752113
发货至: 中国

Quick Overview for GALT 抗体 (AA 251-350) (ABIN752113)

抗原

See all GALT 抗体
GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

适用

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  • 18
  • 12
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
大鼠, 小鼠

宿主

  • 46
  • 7

克隆类型

  • 43
  • 10
多克隆

标记

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  • 3
  • 3
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  • 2
  • 2
  • 2
  • 2
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  • 2
  • 1
  • 1
This GALT antibody is un-conjugated

应用范围

  • 35
  • 18
  • 12
  • 10
  • 6
  • 5
  • 5
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  • 2
  • 2
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

    • 13
    • 8
    • 6
    • 1
    • 1
    AA 251-350

    交叉反应

    小鼠, 大鼠

    预测反应

    Human,Cow

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GALT

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

    别名

    GALT

    背景

    Synonyms: Gal 1 P uridylyltransferase, Galactose 1 phosphate uridyl transferase, Galactose 1 phosphate uridylyltransferase, UDP glucose hexose 1 phosphate uridylyltransferase, GALT_HUMAN.

    Background: GALT (Galactose 1 phosphate uridyl transferase) 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.

    基因ID

    2592
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