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

This anti-DPYS antibody (ABIN1398219) is a Rabbit Polyclonal antibody detecting DPYS in WB, IF (cc), IF (p). Suitable for Human.
产品编号 ABIN1398219
发货至: 中国

Quick Overview for DPYS 抗体 (AA 121-220) (AbBy Fluor® 350) (ABIN1398219)

抗原

See all DPYS 抗体
DPYS (Dihydropyrimidinase (DPYS))

适用

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宿主

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克隆类型

  • 46
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多克隆

标记

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This DPYS antibody is conjugated to AbBy Fluor® 350

应用范围

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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
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    AA 121-220

    预测反应

    Human,Mouse,Rat,Dog,Cow,Sheep,Chicken

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human DHP/Dihydropyrimidinase

    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

    DPYS (Dihydropyrimidinase (DPYS))

    别名

    Dihydropyrimidinase

    背景

    Synonyms: DHP, DHPase, Dihydropyrimidinase, Dihydropyrimidine amidohydrolase, Dpys, DPYS_HUMAN, Hydantoinase.

    Background: Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

    基因ID

    1807
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