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NOTCH3 抗体 (AA 2291-2321)

NOTCH3 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 487CT6-9-2 unconjugated
产品编号 ABIN3032031
发货至: 中国
  • 抗原 See all NOTCH3 抗体
    NOTCH3 (Notch 3 (NOTCH3))
    抗原表位
    • 14
    • 10
    • 7
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    AA 2291-2321
    适用
    • 49
    • 16
    • 11
    • 1
    宿主
    • 34
    • 15
    • 2
    • 1
    • 1
    小鼠
    克隆类型
    • 38
    • 16
    单克隆
    标记
    • 29
    • 5
    • 4
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NOTCH3 antibody is un-conjugated
    应用范围
    • 26
    • 24
    • 22
    • 9
    • 7
    • 4
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Purified
    免疫原
    A portion of amino acids 2291-2321 from the human protein was used as the immunogen for this NOTCH3 antibody.
    克隆位点
    487CT6-9-2
    亚型
    IgG1
    Top Product
    Discover our top product NOTCH3 Primary Antibody
  • 应用备注
    Titration of the NOTCH3 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:100-1:250
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    In 1X PBS, pH 7.4, with 0.09 % 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
    -20 °C
    储存方法
    Aliquot the NOTCH3 antibody and store frozen at -20°C or colder. Avoid repeated 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
    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). [provided by RefSeq].
    UniProt
    Q9UM47
    途径
    Notch Signaling
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