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Phospho-SRC (Tyr419) Recombinant Rabbit mAb (S-1182-5)

Proto-oncogene tyrosine-protein kinase Src,Proto-oncogene c-Src,pp60c-src (p60-Src)

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B0832
规格
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产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    Phospho-SRC (Tyr419)
  • 分子别名

    Proto-oncogene tyrosine-protein kinase Src, Proto-oncogene c-Src, pp60c-src (p60-Src)
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Cell membrane, Cytoplasm, Nucleus
  • Accession

    P12931
  • 克隆号

    S-1182-5
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 翻译后修饰类型

    磷酸化
  • 应用

    ICC ? ,
    WB ,
    IP
  • 反应种属 ?

    Hu, Rt
  • 预测反应种属
    (反应种属缩写表)

    Zf, Fs, Rt, Ms, Av, Dg, Xe, Bv, Pg
  • 纯化方式

    Protein A
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

稀释度
应用 稀释度
Dot Blot 1:1000
WB 1:1000
IP 1:50
ICC 1:100
背景介绍
  • Proto-oncogene tyrosine-protein kinase Src, also known as proto-oncogene c-Src, or simply c-Src belongs to a family of Src family kinases. c-Src phosphorylates specific tyrosine residues in other tyrosine kinases. It plays a role in the regulation of embryonic development and cell growth. An elevated level of activity of c-Src is suggested to be linked to cancer progression by promoting other signals. Mutations in c-Src could be involved in the malignant progression of colon cancer. The activation of c-Src causes the dephosphorylation of the tyrosine 527. This induces long-range allostery via protein domain dynamics, causing the structure to be destabilized, resulting in the opening up of the SH3, SH2 and kinase domains and the autophosphorylation of the residue tyrosine 419.

  • 免疫印迹

    • WB result of Phospho-SRC (Tyr419) Recombinant Rabbit mAb
      Primary antibody: Phospho-SRC (Tyr419) Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: untreated A431 whole cell lysate 20 µg
      Lane 2: A431 treated with 50 mM pervanadate for 5 minutes whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 60 kDa
      Observed MW: 60 kDa

    • WB result of Phospho-SRC (Tyr419) Recombinant Rabbit mAb
      Primary antibody: Phospho-SRC (Tyr419) Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: Untreated C6 whole cell lysate 20 µg
      Lane 2: C6 treated with pervanadate(10mM, 20min) whole cell lysate 20 µg
      Negative control: Untreated C6 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution Predicted MW: 60 kDa
      Observed MW: 60kDa

  • 免疫沉淀

    • Phospho-SRC (Tyr419) Recombinan Rabbit mAb at 1/50 dilution (1 µg) immunoprecipitating Phospho-SRC (Tyr419) in 0.4 mg A431 treated with 50mM pervanadate for 5 minutes whole cell lysate.
      Western blot was performed on the immunoprecipitate using Phospho-SRC (Tyr419) Recombinan Rabbit mAb at 1/1000 dilution.
      Secondary antibody (HRP) for IP was used at 1/1000 dilution.
      Lane 1: A431 treated with 50mM pervanadate for 5 minutes whole cell lysate 20 µg (Input)
      Lane 2: Phospho-SRC (Tyr419) Rabbit mAb IP in A431 treated with 50mM pervanadate for 5 minutes whole cell lysate
      Lane 3: Rabbit monoclonal IgG IP in A431 treated with 50mM pervanadate for 5 minutes whole cell lysate
      Predicted MW: 60 kDa
      Observed MW: 60kDa

  • 斑点杂交

    • Dot blot result of Phospho-SRC (Tyr419) Recombinant Rabbit mAb
      Lane 1: Phospho-SRC (Tyr419) peptide
      Lane 2: SRC unmodified peptide
      Primary antibody: Phospho-SRC (Tyr419) Recombinant Rabbit mAb at 1/1000 dilution
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution

  • 免疫细胞化学

    • ICC analysis of A431 cells treated with 50mM pervanadate for 5 minutes (top panel) and untreated A431 cells (below panel). Anti- Phospho-SRC (Tyr419) antibody was used at 1/100 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).

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