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SOS1 抗体 (AA 1283-1333)

SOS1 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7452055
发货至: 中国
  • 抗原 See all SOS1 抗体
    SOS1 (Son of Sevenless Homolog 1 (SOS1))
    抗原表位
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1283-1333
    适用
    • 23
    • 10
    • 5
    • 5
    • 5
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    宿主
    • 15
    • 10
    • 1
    克隆类型
    • 17
    • 9
    多克隆
    标记
    • 23
    • 1
    • 1
    • 1
    This SOS1 antibody is un-conjugated
    应用范围
    • 18
    • 14
    • 7
    • 3
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    原理
    Rabbit anti-SOS1 Antibody, Affinity Purified
    预测反应
    Mouse
    纯化方法
    Affinity Purified
    免疫原
    between AA 1283 and 1333
    亚型
    IgG
    Top Product
    Discover our top product SOS1 Primary Antibody
  • 应用备注

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    限制
    仅限研究用
  • 浓度
    200 μg/mL
    缓冲液
    Tris-buffered Saline containing 0.1 % BSA and 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
    4 °C
    有效期
    12 months
  • 抗原
    SOS1 (Son of Sevenless Homolog 1 (SOS1))
    别名
    SOS1 (SOS1 产品)
    别名
    GF1 antibody, GGF1 antibody, GINGF antibody, HGF antibody, NS4 antibody, 4430401P03Rik antibody, 9630010N06 antibody, AI449023 antibody, SOS Ras/Rac guanine nucleotide exchange factor 1 antibody, son of sevenless homolog 1 (Drosophila) antibody, SOS1 antibody, Sos1 antibody
    背景
    Background: SOS1 (son of sevenless homolog 1) is a human paralog of the drosophila SOS gene. Drosophila SOS was originally identified as a gene that functioned downstream of the sevenless gene in the Ras/MAP kinase signaling pathway. SOS and its paralogs, SOS1 and SOS2, function as guanine nucleotide exchange factors that act on Ras-GTPases to cause release of GDP in exchange for GTP. Mutations in SOS1 are the cause of Noonan syndrome type 4 and gingival fibromatosis.
    基因ID
    6654
    NCBI登录号
    NP_005624
    UniProt
    Q07889
    途径
    RTK signaling, TCR Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Hepatitis C, Signaling Events mediated by VEGFR1 and VEGFR2, Signaling of Hepatocyte Growth Factor Receptor, BCR Signaling
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