首页 > 产品目录 > 免疫学 > 抗体 > Anti-p38 (phospho T180 + Y182) antibody

Anti-p38 (phospho T180 + Y182) antibody

产品编号 :
英文名称 :
中文名称 :
产品等级 :
品牌 :
包装规格 交货周期 质量标准 目录价 会员专享价 数量
50uL
- +
产品详情
  • 产品名称

    Anti-p38 (phospho T180 + Y182)抗体
    参阅全部 p38 一抗

  • 描述

    兔多克隆抗体to p38 (phospho T180 + Y182)

  • 宿主

    Rabbit

  • 经测试应用

    适用于: IHC-PICC/IFWBmore details

  • 种属反应性

    与反应: Rat, Human
    预测可用于: Mouse, Dog, Carp, Monkey

  • 免疫原

    Synthetic peptide corresponding to Human p38 (phospho T180 + Y182). p38 is dually phosphorylated and therefore fully activated by MEK3 and MEK6 on threonine 180 and tyrosine 182 within the activation loop.
    Database link: 
    Q16539
    (Peptide available as ab5253)

  • 阳性对照

    • WB: HeLa, A431, COLO 205, A549 and A549 cell lysate; HEK-293 (human epithelial cell line from embryonic kidney) cells. IHC-P: Human brain tissue, human heart tissue, rat heart tissue. ICC: SH-SY5Y (human neuroblastoma cell line from bone marrow) cells.

  • 常规说明


    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

  • 形式

    Liquid

  • 存放说明

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle.

  • 存储溶液

    pH: 7.30
    Preservative: 0.05% Sodium azide
    Constituents: PBS, 50% Glycerol, 0.1% BSA

    BSA is IgG and protease free. PBS without Mg2+ and Ca2+.

  • 浓度

    • 50 µl 浓度为 0.2 mg/ml

  • 纯度

    Protein A purified

  • 纯化说明

    Purified from rabbit serum by sequential epitope-specific chromatography. The antibody has been negatively preadsorbed using i) non-phosphopeptide corresponding to the site of phosphorylation to remove antibody that is reactive with non-phosphorylated p38, and ii) a JNK-derived peptide that is phosphorylated at threonine 183 and tyrosine 185. The final product is generated by affinity chromatography using a p38-derived peptide that is phosphorylated at threonine 180 and tyrosine 182.

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab4822于以下的经测试应用

“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。

应用Ab评论说明
IHC-P

1/10 - 1/100.

ICC/IF

1/250.

WB(3)

1/1000. Predicted molecular weight: 38 kDa.

数据库链接

别名

  • CSAID Binding Protein 1 antibody

  • CSAID binding protein antibody

  • CSAID-binding protein antibody

  • Csaids binding protein antibody

  • CSBP 1 antibody

  • CSBP 2 antibody

  • CSBP antibody

  • CSBP1 antibody

  • CSBP2 antibody

  • CSPB1 antibody

  • Cytokine suppressive anti-inflammatory drug-binding protein antibody

  • EXIP antibody

  • MAP kinase 14 antibody

  • MAP kinase MXI2 antibody

  • MAP kinase p38 alpha antibody

  • MAPK 14 antibody

  • MAPK14 antibody

  • MAX interacting protein 2 antibody

  • MAX-interacting protein 2 antibody

  • Mitogen Activated Protein Kinase 14 antibody

  • Mitogen activated protein kinase p38 alpha antibody

  • Mitogen-activated protein kinase 14 antibody

  • Mitogen-activated protein kinase p38 alpha antibody

  • MK14_HUMAN antibody

  • Mxi 2 antibody

  • MXI2 antibody

  • p38 ALPHA antibody

  • p38 antibody

  • p38 MAP kinase antibody

  • p38 MAPK antibody

  • p38 mitogen activated protein kinase antibody

  • p38ALPHA antibody

  • p38alpha Exip antibody

  • PRKM14 antibody

  • PRKM15 antibody

  • RK antibody

  • SAPK2A antibody

  • Stress-activated protein kinase 2a antibody

  • Western blot - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Western blot - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    All lanes : Anti-p38 (phospho T180 + Y182) antibody (ab4822) at 1/1000 dilution

    Lane 1 : HeLa (human epithelial cell line from cervix adenocarcinoma) cell lysate
    Lane 2 : HeLa (human epithelial cell line from cervix adenocarcinoma) exposed for 40 min with UV, cell lysate
    Lane 3 : A431 (human epidermoid carcinoma cell line) cell lysate
    Lane 4 : A431 (human epidermoid carcinoma cell line) exposed for 40 min with UV, cell lysate
    Lane 5 : COLO 205 (human colon adenocarcinoma cell line) cell lysate
    Lane 6 : COLO 205 (human colon adenocarcinoma cell line) exposed for 40 min with UV, cell lysate
    Lane 7 : A549 (human lung carcinoma cell line) cell lysate
    Lane 8 : A549 (human lung carcinoma cell line) exposed for 40 min with UV, cell lysate

    Lysates/proteins at 20 µg per lane.

    Secondary
    All lanes : Goat anti-Rabbit IgG HRP at 1/5000 dilution

    Developed using the ECL technique.

    Predicted band size: 38 kDa

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Paraffin-embedded human brain tissue stained for p38 (phospho T180 + Y182) using ab4822 (right panel) at 1/100 dilution in immunohistochemical analysis followed by HRP-conjugated secondary antibody and DAB staining. Negative control (left panel) staining without primary antibody. 

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Paraffin-embedded human heart tissue stained for p38 (phospho T180 + Y182) using ab4822 (right panel) at 1/20 dilution in immunohistochemical analysis followed by HRP-conjugated secondary antibody and DAB staining. Negative control (left panel) staining without primary antibody.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Paraffin-embedded rat heart tissue stained for p38 (phospho T180 + Y182) using ab4822 (right panel) at 1/20 dilution in immunohistochemical analysis followed by HRP-conjugated secondary antibody and DAB staining. Negative control (left panel) staining without primary antibody.

  • Immunocytochemistry/ Immunofluorescence - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Immunocytochemistry/ Immunofluorescence - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    4% PFA-fixed, Triton X-100 permeabilized SH-SY5Y (human neuroblastoma cell line from bone marrow) cells labeling p38 (phospho T180 + Y182) (Panel A: green) using ab4822 at 1 µg/mL in ICC/IF. Secondary antibody: Alexa Flour® 488 Goat Anti-Rabbit IgG at 1/400 dilution. Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI. F-actin (Panel c: red) was stained with Alexa Fluor® 594 Phalloidin. Panel d is a merged image showing nuclear localization. Panel e is a no primary antibody control. 

     

  • Western blot - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Western blot - Anti-p38 (phospho T180 + Y182) antibody (ab4822)

    Peptide Competition: Extracts prepared from HEK-293 (human epithelial cell line from embryonic kidney) cells treated with UV irradiation were resolved on a 10% Tris-glycine gel and transferred to nitrocellulose. Membranes were blocked with a 5% BSA-TBST buffer overnight at 4oC, then were incubated with 0.50 µg/mL ab4822 for two hours at room temperature in a 3% BSA-TBST buffer, following its prior incubation with: the peptide immunogen (1), a generic phosphothreonine containing peptide (2), a generic phosphotyrosine-containing peptide (3), the non-phosphorylated peptide corresponding to the phosphopeptide (4), no peptide (5), the phosphorylated peptide derived from the corresponding region of JNK 1 & 2 (6), and, the phosphorylated peptide derived from the corresponding region of ERK 1 & 2 (7). After washing, membranes were incubated with goat F(ab')2 antirabbit IgG alkaline phosphatase and the signal was detected using the Tropix WesternStar method. The data show that only the phosphopeptide


浏览记录

抱歉,暂无浏览记录