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Bad Recombinant Rabbit mAb (S-976-26)

Bad Recombinant Rabbit mAb (S-976-26)

货号: S0B0686
价格: 600
规格: 25μl
介绍: -
其他: -
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
  • 应用

    IHC-P, WB, IP
  • 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

稀释度
应用 稀释度
WB 1:1000
IP 1:50
IHC-P 1:250
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.