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UROD 抗体 (AA 121-220) (AbBy Fluor® 350)

This AbBy Fluor® 350-conjugated 兔 多克隆 anti-UROD antibody specifically detects UROD in WB, IF (cc) 和 IF (p). The antibody is reactive with 人 samples.
产品编号 ABIN919371
发货至: 中国
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Quick Overview for UROD 抗体 (AA 121-220) (AbBy Fluor® 350) (ABIN919371)

抗原

See all UROD 抗体
UROD (Uroporphyrinogen Decarboxylase (UROD))

适用

  • 37
  • 9
  • 6
  • 3
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  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 33
  • 6
  • 1

克隆类型

  • 37
  • 3
多克隆

标记

  • 21
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
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This UROD antibody is conjugated to AbBy Fluor® 350

应用范围

  • 33
  • 12
  • 12
  • 9
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 121-220

    交叉反应

    预测反应

    Mouse,Rat,Dog,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human UROD

    亚型

    IgG
  • 应用备注

    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

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    UROD (Uroporphyrinogen Decarboxylase (UROD))

    别名

    UROD

    背景

    Synonyms: PCT, UPD, URO D, Uroporphyrinogen decarboxylase, Uroporphyrinogen III decarboxylase.

    Background: UROD is the fifth enzyme of the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria. Porphyria cutanea tarda is an autosomal dominant disorder characterized by light-sensitive dermatitis and associated with the excretion of large amounts of uroporphyrin in urine. Hepatoerythropoetic porphyria is a form of porphyria cutanae tarda that may also be a manifestation of benign or malignant hepatic tumors.

    基因ID

    79842
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