您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
JNK1 Recombinant Rabbit mAb (S-1153-21)

JNK1 Recombinant Rabbit mAb (S-1153-21)

货号: S0B0859
价格: 260
规格: 10μl
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    JNK1
  • 分子别名

    Mitogen-activated protein kinase 8; MAP kinase 8; MAPK 8; Stress-activated protein kinase JNK1; c-Jun N-terminal kinase 1; Prkm8
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Cytoplasm, Nucleus
  • Accession

    Q91Y86
  • 克隆号

    S-1153-21
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    ICFCM, IHC-P, ICC, 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
ICC 1:100
ICFCM 1:500
背景介绍
  • JNK1, also known as c-Jun N-terminal kinase 1, is a member of the mitogen-activated protein kinase (MAPK) family of enzymes that play essential roles in cellular signaling pathways. JNK1 is primarily involved in the cellular response to stress. JNK1 is activated by a complex signaling cascade involving upstream kinases, such as MEKK1, MLK3, and ASK1. Activation typically occurs in response to stress stimuli, which trigger the assembly of a multi-protein complex known as the MAPKKK-MAPKK-MAPK module. This complex leads to the phosphorylation and activation of JNK1, which then phosphorylates its downstream targets. Upon activation, it phosphorylates specific substrates, including transcription factors such as c-Jun, ATF2, and p53, leading to changes in gene expression that help cells adapt to stress. JNK1 plays a dual role in regulating cell death (apoptosis) and survival. Depending on the cellular context and stimuli, JNK1 can either promote or inhibit apoptosis. JNK1 is also involved in inflammatory and immune responses. It can regulate the production of cytokines, chemokines, and other inflammatory mediators, as well as modulate the activation and function of immune cells.

  • 免疫印迹

    • WB result of JNK1 Recombinant Rabbit mAb
      Primary antibody: JNK1 Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: A431 whole cell lysate 20 µg
      Lane 2: HeLa whole cell lysate 20 µg
      Lane 3: Jurkat whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 44 kDa
      Observed MW: 38, 50 kDa

    • WB result of JNK1 Recombinant Rabbit mAb
      Primary antibody: JNK1 Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: NIH/3T3 whole cell lysate 20 µg
      Lane 2: Neuro-2a whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 44 kDa
      Observed MW: 38, 50 kDa

    • WB result of JNK1 Recombinant Rabbit mAb
      Primary antibody: JNK1 Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: PC-12 whole cell lysate 20 µg
      Lane 2: C6 whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 44 kDa
      Observed MW: 38, 50 kDa

  • 流式分析

    • Flow cytometric analysis of 4% PFA fixed 90% methanol permeabilized HeLa (Human cervix adenocarcinoma epithelial cell) labelling JNK1 antibody at 1/500 dilution (0.1 μg) / (Red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti - Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody.

  • 免疫沉淀

    • JNK1 Rabbit mAb at 1/50 dilution (1 µg) immunoprecipitating JNK1 in 0.4 mg Neuro-2a whole cell lysate.
      Western blot was performed on the immunoprecipitate using JNK1 Rabbit mAb at 1/1000 dilution.
      Secondary antibody (HRP) for IP was used at 1/1000 dilution.
      Lane 1: Neuro-2a whole cell lysate 20 µg (Input)
      Lane 2: JNK1 Rabbit mAb IP in Neuro-2a whole cell lysate
      Lane 3: Rabbit monoclonal IgG IP in Neuro-2a whole cell lysate
      Predicted MW: 44 kDa
      Observed MW: 38, 50 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human ovarian carcinoma. Anti-JNK1 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 prostatic carcinoma. Anti-JNK1 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 cerebral cortex. Anti-JNK1 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 testis. Anti-JNK1 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 testis. Anti-JNK1 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.

  • 免疫细胞化学

    • ICC shows positive staining in HeLa cells. Anti-JNK1 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).