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NOTCH3 抗体 (AA 47-156)

NOTCH3 适用: 人 ELISA 宿主: 小鼠 Monoclonal 3E2D9 unconjugated
产品编号 ABIN5542534
发货至: 中国
  • 抗原 See all NOTCH3 抗体
    NOTCH3 (Notch 3 (NOTCH3))
    抗原表位
    • 14
    • 11
    • 7
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    AA 47-156
    适用
    • 49
    • 17
    • 11
    • 1
    宿主
    • 34
    • 15
    • 3
    • 1
    • 1
    小鼠
    克隆类型
    • 38
    • 17
    单克隆
    标记
    • 29
    • 5
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NOTCH3 antibody is un-conjugated
    应用范围
    • 26
    • 23
    • 20
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    ELISA
    原理
    Notch3 Antibody
    纯化方法
    Purified antibody
    免疫原
    Purified recombinant fragment of human Notch3 (AA: 47-156) expressed in E. Coli.
    克隆位点
    3E2D9
    亚型
    IgG2a
    Top Product
    Discover our top product NOTCH3 Primary Antibody
  • 应用备注
    ELISA: 1/10000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified antibody in PBS with 0.05 % 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
    4 °C,-20 °C
    储存方法
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • 抗原
    NOTCH3 (Notch 3 (NOTCH3))
    别名
    Notch3 (NOTCH3 产品)
    别名
    CADASIL antibody, CASIL antibody, IMF2 antibody, AW229011 antibody, N3 antibody, hpbk antibody, fa14b08 antibody, notch5 antibody, wu:fa14b08 antibody, notch 3 antibody, NOTCH3 antibody, Notch3 antibody, notch3 antibody
    背景

    Description: This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

    Aliases: IMF2, CASIL, CADASIL

    分子量
    243.6kDa
    基因ID
    4854
    HGNC
    4854
    UniProt
    Q9UM47
    途径
    Notch Signaling
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