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Anti-Cytokeratin 18 antibody

Anti-Cytokeratin 18 antibody
别名: Cytokeratin 18
储存条件: -20℃ 
Anti-Cytokeratin 18 antibody
货号 规格 可用库存 销售价(RMB) 您的折扣价(RMB) 购买数量
ZY0407-1-50 μl 50 μl 现货 1200.00 1200
ZY0407-1-100 μl 50 μl 现货 2100.00 2100
熔点:
密度:
储存条件: -20℃

 

Anti-Cytokeratin 18 antibody

  • 概述

  • 产品描述Cytokeratin 18 is an acidic keratin which is found primarily in non squamous epithelia and is present in a majority of adenocarcinomas and ductal carcinomas but not in squamous cell carcinomas. Cytokeratin 18 exists in combination with Cytokeratin 8, a basic keratin. Hepatocellular carcinomas have been reportedly defined by the use of antibodies that recognize only Cytokeratins 8 and 18.

  • 产品名称Anti-Cytokeratin 18 antibody

  • 分子量48 kDa

  • 种属反应性Human,Mouse,Rat

  • 验证应用WB,ICC,IHC-P

  • 抗体类型兔多抗

  • 免疫原This antibody is produced by immunizing rabbits with a synthetic peptide (KLH-coupled) corresponding to a region of C-terminal residues of mouse CK-18.

  • 偶联Non-conjugated

  • 性能

  • 形态Liquid

  • 浓度1 mg/mL.

  • 存放说明Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.

  • 存储缓冲液1*PBS (pH7.4), 0.2% BSA, 25% Glycerol. Preservative: 0.05% Sodium Azide.

  • 亚型IgG

  • 纯化方式Peptide affinity purified.

  • 亚细胞定位Cytoplasm, perinuclear region.

  • 数据链接SwissProt: P05783 Human
    SwissProt: P05784 Mouse
    SwissProt: Q5BJY9 Rat

  • 其它名称Cell proliferation inducing gene 46 protein antibody
    Cell proliferation inducing protein 46 antibody
    Cell proliferation-inducing gene 46 protein antibody
    CK 18 antibody
    CK-18 antibody
    CK18 antibody
    CYK 18 antibody
    CYK18 antibody
    Cytokeratin 18 antibody
    Cytokeratin endo B antibody
    Cytokeratin-18 antibody
    K 18 antibody
    K18 antibody
    K1C18_HUMAN antibody
    KA18 antibody
    Keratin 18 antibody
    Keratin 18, type I antibody
    Keratin D antibody
    keratin, type I cytoskeletal 18 antibody
    Keratin-18 antibody
    Krt18 antibody

    more
  • 应用

    WB:1:25,000-50,000
    ICC:1:200
    IHC-P:1:100

  •  

    Fig1: Western blot analysis of Cytokeratin 18 on mouse liver tissue lysate. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody was used at a 1:500 dilution in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.

     

    Fig2: ICC staining Cytokeratin 18 in 293T cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the antibodyat a dilution of 1:100 for 1 hour at room temperature, washed with PBS. Alexa Fluorc™ 488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/100 dilution. The nuclear counter stain is DAPI (blue).

     

    Fig3: ICC staining Cytokeratin 18 in A549 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the antibodyat a dilution of 1:100 for 1 hour at room temperature, washed with PBS. Alexa Fluorc™ 488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/100 dilution. The nuclear counter stain is DAPI (blue).

     

    Fig4: ICC staining Cytokeratin 18 in SW480 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the antibodyat a dilution of 1:100 for 1 hour at room temperature, washed with PBS. Alexa Fluorc™ 488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/100 dilution. The nuclear counter stain is DAPI (blue).

     

    Fig5: Immunohistochemical analysis of paraffin-embedded mouse lung tissue using anti-Cytokeratin 18 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the antibodyat 1/100 dilution, for 30 minutes at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chrogen. Counter stained with hematoxylin and mounted with DPX.

     

    Fig6: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-Cytokeratin 18 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the antibody  at 1/100 dilution, for 30 minutes at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chrogen. Counter stained with hematoxylin and mounted with DPX.

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