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QDPR 抗体 (Middle Region) (Biotin)

The Biotin-conjugated 兔 多克隆 anti-QDPR antibody (ABIN8029486) specifically detects QDPR in WB, ELISA 和 IHC. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN8029486
发货至: 中国
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Quick Overview for QDPR 抗体 (Middle Region) (Biotin) (ABIN8029486)

抗原

See all QDPR 抗体
QDPR (Quinoid Dihydropteridine Reductase (QDPR))

适用

人, 小鼠, 大鼠

宿主

  • 44
  • 4

克隆类型

  • 45
  • 3
多克隆

标记

  • 17
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
This QDPR antibody is conjugated to Biotin

应用范围

  • 23
  • 16
  • 8
  • 8
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • 抗原表位

    • 11
    • 8
    • 6
    • 5
    • 2
    • 1
    Middle Region

    原理

    Anti-QDPR Antibody Biotin Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    纯化方法

    Immunogen affinity purified.

    免疫原

    A synthetic peptide corresponding to a sequence in the middle region of human QDPR.

    亚型

    IgG
  • 应用备注

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    储存液

    Sodium azide

    注意事项

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

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    QDPR (Quinoid Dihydropteridine Reductase (QDPR))

    别名

    QDPR

    背景

    Background: This gene encodes the enzyme dihydropteridine reductase, which catalyzes the NADH-mediated reduction of quinonoid dihydrobiopterin. This enzyme is an essential component of the pterin-dependent aromatic amino acid hydroxylating systems. Mutations in this gene resulting in QDPR deficiency include aberrant splicing, amino acid substitutions, insertions, or premature terminations. Dihydropteridine reductase deficiency presents as atypical phenylketonuria due to insufficient production of biopterin, a cofactor for phenylalanine hydroxylase.

    Gene Full Name: quinoid dihydropteridine reductase

    基因ID

    5860

    UniProt

    P09417
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