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UPB1 抗体

The 兔 多克隆 anti-UPB1 antibody is suitable to detect UPB1 in samples from 人, 小鼠, 大鼠, 犬, 斑马鱼, Drosophila melanogaster, Arabidopsis 和 C. elegans. It has been validated for WB 和 ELISA.
产品编号 ABIN2462585
发货至: 中国
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for UPB1 抗体 (ABIN2462585)

抗原

See all UPB1 抗体
UPB1 (Ureidopropionase, beta (UPB1))

适用

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人, 小鼠, 大鼠, 犬, 斑马鱼, Drosophila melanogaster, Arabidopsis, C. elegans

宿主

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克隆类型

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多克隆

标记

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This UPB1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by protein A chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human UPB1.
  • 应用备注

    UPB1 antibody can be used for detection of UPB1 by ELISA at 1:1562500. UPB1 antibody can be used for detection of UPB1 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store UPB1 antibody at -20 °C.
  • 抗原

    UPB1 (Ureidopropionase, beta (UPB1))

    别名

    UPB1

    背景

    UPB1 is a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activityThis gene encodes a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity.

    分子量

    42 kDa

    基因ID

    51733

    NCBI登录号

    NP_057411

    UniProt

    Q9UBR1
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