Anti-SUB1 Antibody (monoclonal,  8D9D1)(M02698-3-50ul)

Anti-SUB1 Antibody (monoclonal

, 8D9D1)(M02698-3-50ul)
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  • ¥1180
  • BOSTER已认证
  • M02698-3-50ul
  • 中国
  • 2025年07月08日
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    • 技术资料
    • 库存

      大量

    • 供应商

      广州威佳科技有限公司

    • 规格

      50ul

    产品概况

    货号 M02698-3
    产品名称 Anti-SUB1 Antibody (monoclonal, 8D9D1)
    基因名 SUB1
    抗体来源 Mouse
    克隆 Monoclonal
    抗体亚型 Mouse IgG2b
    分子量 19KD
    免疫原 E.coli-derived human PC4/SUB1 recombinant protein (Position: N62-L127).
    内容 500 ug/ml antibody with PBS,0.02% NaN3, 1 mg BSA and 50% glycerol.
    纯化方式 Immunogen affinity purified.
    浓度 500 ug/ml
    产品形态 Liquid
    保存条件 12 months from date of receipt,-20℃ as supplied. 6 months 2 to 8℃ after reconstitution. Avoid repeated freezing and thawing.
    背景资料 Activated RNA polymerase II transcriptional coactivator p15, also known as positive cofactor 4 (PC4) or SUB1 homolog, is a protein that in humans is encoded by the SUB1 gene. This gene is mapped to 5p13.3. The transcriptional cofactor PC4 is an ancient single-strand DNA (ssDNA)-binding protein that has a homologue in bacteriophage T5 where it is likely the elusive replicative ssDNA-binding protein. The recombinant PC4 is shown to function identically to the native protein through its interaction with TAFs.
    研究类别 1. "Entrez Gene SUB1: SUB1 homolog (S. cerevisiae)".2. Kretzschmar M, Kaiser K, Lottspeich F, Meisterernst M (August 1994). "A novel mediator of class II gene transcription with homology to viral immediate-early transcriptional regulators". Cell 78 (3): 525–34.3. Ge H, Roeder RG (August 1994). "Purification, cloning, and characterization of a human coactivator, PC4, that mediates transcriptional activation of class II genes". Cell 78 (3): 513–23.
    Uniprot ID SUB1: P53999
    推荐配套的二抗和检测试剂 Boster recommends Enhanced Chemiluminescent Kit with anti-Mouse IgG (EK1001) for Western blot, and HRP Conjugated anti-Mouse IgG Super Vision Assay Kit (SV0001-1) for IHC(P).

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    [list_product_images]Figure 1. Western blot analysis of anti- SUB1 antibody (M02698-3). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
    Lane 1: Hela whole cell lysates,
    Lane 2: A549 whole cell lysates,
    Lane 3: MCF-7 whole cell lysates,
    Lane 4: T47D whole cell lysates,
    Lane 5: rat liver tissue lysates,
    Lane 6: rat spleen tissue lysates,
    Lane 7: mouse spleen tissue lysates.
    Use mouse anti- SUB1 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for SUB1 at approximately 19KD. The expected band size for SUB1 is at 14KD.|Figure 2. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of mouse liver tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 3. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of rat liver tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 4. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human laryngeal squamous cell carcinomatissue tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 5. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human testicular germ cell tumors tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 6. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 7. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human Colorectal adenocarcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 8. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human hepatocellular carcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 9. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human hepatocellular carcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 10. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human Lung adenocarcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 11. IHC analysis using anti- SUB1 antibody (M02698-3). detected in paraffin-embedded section of human spleen tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.|Figure 12. IF analysis using anti- SUB1 antibody (M02698-3).detected in paraffin-embedded section of human intestinal cancer tissues. The tissue section were stained using the cy3-conjugated Anti-mouse IgG Secondary Antibody (red)(Catalog#BA1031) and counterstained with DAPI (blue).|Figure 13. Flow cytometry analysis of HepG2 cell (1x106) DyLight 488 conjugated goat anti-mouse IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG DyLight 488. Unlabelled sample (Red line).[/list_product_images]

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