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DLL3 抗体 (AA 62-286)

DLL3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5027148
发货至: 中国
  • 抗原 See all DLL3 抗体
    DLL3 (delta Like Protein 3 (DLL3))
    抗原表位
    • 11
    • 7
    • 6
    • 6
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 62-286
    适用
    • 52
    • 24
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    宿主
    • 53
    • 2
    克隆类型
    • 53
    • 2
    多克隆
    标记
    • 22
    • 6
    • 5
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DLL3 antibody is un-conjugated
    应用范围
    • 50
    • 27
    • 21
    • 19
    • 10
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    纯化方法
    Protein A Chromatography
    免疫原
    A partial length recombinant Delta like 3 protein (amino acids 62-286) was used as the immunogen for this antibody.
    亚型
    IgG
    Top Product
    Discover our top product DLL3 Primary Antibody
  • 应用备注
    WB: 2-4 μg/mL
    限制
    仅限研究用
  • 浓度
    0.5 mg/mL
    缓冲液
    PBS containing 0.05 % BSA, PH 7.4
    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 the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
  • 抗原
    DLL3 (delta Like Protein 3 (DLL3))
    别名
    Delta like 3 (DLL3 产品)
    别名
    SCDO1 antibody, pu antibody, pudgy antibody, delta like canonical Notch ligand 3 antibody, delta-like 3 (Drosophila) antibody, DLL3 antibody, Dll3 antibody
    背景
    Delta like 3 (DLL3) is a member of Delta/Serrate/Lag2 (DSL) ligands for Notch receptors and plays a role in Notch signaling. Out of Five DSL ligands, DLL3 is the most structurally divergent DSL ligand. DLL3 is expressed throughout the presomitic mesoderm and is localized to the rostral somatic compartments. Homozygous disruptions of Notch1 and DLL3 result in severe abnormalities in somitogenesis. Mutations in the human DLL3 homolog cause recessive skeletal abnormalities in spondylocostal dysostosis with a consistent pattern of abnormal segmentation.
    分子量
    65 kDa
    基因ID
    10683
    UniProt
    Q9NYJ7
    途径
    Notch Signaling
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