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PDCD10 抗体

PDCD10 适用: 人, 小鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6989859
发货至: 中国
  • 抗原 See all PDCD10 抗体
    PDCD10 (Programmed Cell Death 10 (PDCD10))
    适用
    • 47
    • 28
    • 13
    人, 小鼠
    宿主
    • 60
    • 2
    克隆类型
    • 60
    • 2
    多克隆
    标记
    • 20
    • 6
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PDCD10 antibody is un-conjugated
    应用范围
    • 27
    • 25
    • 13
    • 13
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    交叉反应
    人, 小鼠
    纯化方法
    Purified by Protein A.
    免疫原
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-212 of human PDCD10 (NP_009148.2).
    亚型
    IgG
    Top Product
    Discover our top product PDCD10 Primary Antibody
  • 应用备注
    WB 1:300-5000
    IF()
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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 for 12 months.
    有效期
    12 months
  • 抗原
    PDCD10 (Programmed Cell Death 10 (PDCD10))
    别名
    PDCD10 (PDCD10 产品)
    别名
    CCM3 antibody, TFAR15 antibody, 2410003B13Rik antibody, Ccm3 antibody, Tfa15 antibody, Tfar15 antibody, zgc:85629 antibody, ccm3a antibody, pdcd10 antibody, zgc:65826 antibody, programmed cell death 10 antibody, programmed cell death 10 S homeolog antibody, programmed cell death 10b antibody, programmed cell death 10a antibody, PDCD10 antibody, Pdcd10 antibody, pdcd10.S antibody, pdcd10b antibody, pdcd10a antibody
    背景

    Synonyms: PDCD10,CCM3,TFAR15

    Background: This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified.

    基因ID
    11235
    UniProt
    Q9BUL8
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