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SH3BP2 抗体 (AA 150-200)

SH3BP2 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7450726
发货至: 中国
  • 抗原 See all SH3BP2 抗体
    SH3BP2 (SH3-Domain Binding Protein 2 (SH3BP2))
    抗原表位
    • 7
    • 7
    • 6
    • 6
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 150-200
    适用
    • 39
    • 13
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    宿主
    • 35
    • 4
    • 1
    克隆类型
    • 38
    • 2
    多克隆
    标记
    • 21
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SH3BP2 antibody is un-conjugated
    应用范围
    • 27
    • 20
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    原理
    Rabbit anti-SH3BP2 Antibody, Affinity Purified
    纯化方法
    Affinity Purified
    免疫原
    between AA 150 and 200
    亚型
    IgG
    Top Product
    Discover our top product SH3BP2 Primary Antibody
  • 应用备注

    IP: 2 - 10 μg/mg lysate

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

    限制
    仅限研究用
  • 浓度
    1000 μg/mL
    缓冲液
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 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
    SH3BP2 (SH3-Domain Binding Protein 2 (SH3BP2))
    别名
    SH3BP2 (SH3BP2 产品)
    别名
    SH3BP2 antibody, 3BP-2 antibody, 3BP2 antibody, CRBM antibody, CRPM antibody, SH3 domain binding protein 2 antibody, SH3-domain binding protein 2 antibody, SH3BP2 antibody, Sh3bp2 antibody
    背景
    Background: SH3 domain-binding protein 2 (SH3BP2) N-terminal pleckstrin homology (PH) domain, an SH3-binding proline-rich region, and a C-terminal SH2 domain. The protein binds to the SH3 domains of several proteins including the ABL1 and SYK protein tyrosine kinases, and functions as a cytoplasmic adaptor protein to positively regulate transcriptional activity in T, natural killer (NK), and basophilic cells. Mutations in this gene result in cherubism, an autosomal dominant inherited syndrome characterized by excessive bone degradation of the upper and lower jaws followed by development of fibrous tissue masses and characteristic facial swelling [taken from NCBI Entrez Gene (Gene ID: 6452)].
    基因ID
    6452
    NCBI登录号
    NP_001116153
    UniProt
    P78314
    途径
    TCR Signaling
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