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UPB1 抗体 (Middle Region)

UPB1 适用: 人, 小鼠, 大鼠, 犬, 斑马鱼, Drosophila melanogaster, Arabidopsis, C. elegans WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN629651
发货至: 中国
  • 抗原 See all UPB1 抗体
    UPB1 (Ureidopropionase, beta (UPB1))
    抗原表位
    • 2
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    Middle Region
    适用
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    人, 小鼠, 大鼠, 犬, 斑马鱼, Drosophila melanogaster, Arabidopsis, C. elegans
    宿主
    • 12
    • 2
    克隆类型
    • 12
    • 2
    多克隆
    标记
    • 14
    This UPB1 antibody is un-conjugated
    应用范围
    • 13
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    Western Blotting (WB)
    特异性
    UPB1 antibody was raised against the middle region of UPB1
    纯化方法
    Purified
    免疫原
    UPB1 antibody was raised using the middle region of UPB1 corresponding to a region with amino acids AVVISNSGAVLGKTRKNHIPRVGDFNESTYYMEGNLGHPVFQTQFGRIAV
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    Discover our top product UPB1 Primary Antibody
  • 应用备注
    WB: 2.5 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    UPB1 Blocking Peptide, catalog no. 33R-1619, is also available for use as a blocking control in assays to test for specificity of this UPB1 antibody

    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of UPB1 antibody in PBS
    浓度
    Lot specific
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 抗原
    UPB1 (Ureidopropionase, beta (UPB1))
    别名
    UPB1 (UPB1 产品)
    别名
    MGC82230 antibody, wu:fb69e03 antibody, zgc:64020 antibody, BUP1 antibody, AI195023 antibody, Bup1 antibody, ureidopropionase, beta S homeolog antibody, beta-ureidopropionase 1 antibody, ureidopropionase, beta antibody, UreidoPropionase Beta antibody, upb1.S antibody, UPB1 antibody, upb1 antibody, upb-1 antibody, Upb1 antibody
    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 activity.
    分子量
    42 kDa (MW of target protein)
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