产品中心 抗体 其他一抗

所有图片(1/10)

Bad Recombinant Rabbit mAb (S-976-26)

Bcl2-associated agonist of cell death,Bcl-2-binding component 6,Bcl-2-like protein 8 (Bcl2-L-8),Bcl-xL/Bcl-2-associated death promoter,Bcl2 antagonist of cell death,BBC6,BCL2L8

价格 600.00 供应商现货 : 3-5个工作日
货号 S0B0686
规格
数量
收藏 分享

产品介绍 FAQs 评论(0)

产品规格
  • 宿主来源

    Rabbit
  • 分子别名

    Bcl2-associated agonist of cell death, Bcl-2-binding component 6, Bcl-2-like protein 8 (Bcl2-L-8), Bcl-xL/Bcl-2-associated death promoter, Bcl2 antagonist of cell death, BBC6, BCL2L8
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Cytoplasm
  • Accession

    Q92934
  • 克隆号

    S-976-26
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 反应种属 ?

    Hu, Ms, Rt
  • 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

  • 应用

    IHC-P ? ,
    WB ,
    IP
  • 稀释度

    应用 稀释度 推荐种属
    WB 1:1000 Hu, Ms, Rt
    IP 1:50 Hu
    IHC-P 1:250 Hu, Ms, Rt
背景介绍
  • BAD protein, or Bcl-2-associated death promoter, is a member of the Bcl-2 protein family that is involved in the regulation of apoptosis (cell death). It functions as a pro-apoptotic protein, promoting cell death when activated. BAD protein interacts with other Bcl-2 family members, such as Bcl-2 and Bcl-xL, to regulate the release of cytochrome c from the mitochondria, which is a crucial step in the apoptotic cascade. The activity of BAD protein is regulated by phosphorylation. When BAD is phosphorylated, it dissociates from Bcl-2 and Bcl-xL, losing its pro-apoptotic function. Conversely, when BAD is dephosphorylated, it binds to Bcl-2 and Bcl-xL, inhibiting their anti-apoptotic activity and promoting apoptosis. The phosphorylation of BAD protein is mediated by several kinases, including AKT (also known as protein kinase B). AKT phosphorylates BAD at specific sites, preventing its interaction with Bcl-2 and Bcl-xL and thus inhibiting apoptosis. This mechanism is important in promoting cell survival and proliferation in response to growth factors and other stimuli.

  • 免疫印迹

    • WB result of Bad Rabbit mAb
      Primary antibody: Bad Rabbit mAb at 1/1000 dilution
      Lane 1: HeLa whole cell lysate 20 µg
      Lane 2: MCF7 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 18 kDa
      Observed MW: 20 kDa

    • WB result of Bad Rabbit mAb
      Primary antibody: Bad Rabbit mAb at 1/1000 dilution
      Lane 1: C2C12 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 18 kDa
      Observed MW: 20 kDa
      (This blot was developed with high sensitivity substrate)

    • WB result of Bad Rabbit mAb
      Primary antibody: Bad Rabbit mAb at 1/1000 dilution
      Lane 1: C6 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 18 kDa
      Observed MW: 20 kDa

  • 免疫沉淀

    • Bad Rabbit mAb at 1/50 dilution (1 µg) immunoprecipitating Bad in 0.4 mg HeLa whole cell lysate.
      Western blot was performed on the immunoprecipitate using Bad Rabbit mAb at 1/1000 dilution.
      Secondary antibody (HRP) for IP was used at 1/1000 dilution.
      Lane 1: HeLa whole cell lysate 20 µg (Input)
      Lane 2: Bad Rabbit mAb IP in HeLa whole cell lysate
      Lane 3: Rabbit monoclonal IgG IP in HeLa whole cell lysate
      Predicted MW: 18 kDa
      Observed MW: 20 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human colon. Anti-Bad antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human kidney. Anti-Bad antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded human skeletal muscle. Anti-Bad antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human colon cancer. Anti-Bad antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse kidney. Anti-Bad antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat kidney. Anti-Bad antibody was used at 1/250 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

FAQs

斯达特公司的抗体,可以回收利用几次?

我们一般不推荐客户回收利用抗体。 因为抗体使用之后缓冲体系已经发生改变,不同客户在回收抗体的保存条件上也会有差异,所以抗体回收使用效果无法保证。另外,我们对一批抗体回收验证测试,测试结果显示不同抗体可回收次数不同,一般效价越高的抗体,可重复使用的次数越多,客户可根据实验情况来确定

评论(0)