电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

UROD 抗体

This anti-UROD antibody is a 兔 多克隆 antibody detecting UROD in WB. Suitable for 人.
产品编号 ABIN2854441
发货至: 中国

Quick Overview for UROD 抗体 (ABIN2854441)

抗原

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

适用

  • 36
  • 10
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 32
  • 7
  • 1

克隆类型

  • 36
  • 4
多克隆

标记

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This UROD antibody is un-conjugated

应用范围

  • 34
  • 13
  • 13
  • 9
  • 9
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 交叉反应

    产品特性

    Rabbit Polyclonal antibody to UROD (uroporphyrinogen decarboxylase)
    UROD antibody [N3C3]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human UROD. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: U87-MG

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): 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

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    UROD (Uroporphyrinogen Decarboxylase (UROD))

    别名

    uroporphyrinogen decarboxylase

    背景

    This gene encodes 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.

    Cellular Localization: Cytoplasm

    分子量

    41 kDa

    基因ID

    7389

    UniProt

    P06132
You are here:
Chat with us!