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T-47D whole cell lysate. View our extensive range of validated lysates from normal and diseased human, mouse and rat tissue.

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Images

Western blot - T-47D whole cell lysate (AB14899), expandable thumbnail
  • Western blot - T-47D whole cell lysate (AB14899), expandable thumbnail
  • Western blot - T-47D whole cell lysate (AB14899), expandable thumbnail
  • Western blot - T-47D whole cell lysate (AB14899), expandable thumbnail
  • Western blot - T-47D whole cell lysate (AB14899), expandable thumbnail

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Key facts

Cell type
T-47D
Species or organism
Human
Form
Liquid

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T-47D whole cell lysate. View our extensive range of validated lysates from normal and diseased human, mouse and rat tissue.

Key facts

Cell type
T-47D
Form
Liquid
Concentration
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Storage

Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
-80°C
Appropriate long-term storage conditions
-80°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Notes

Extracts have been quality control tested by Western blot and the Electrophoretic Mobility Shift Assay (EMSA).

Product promise

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6 product images

  • Western blot - T-47D whole cell lysate (ab14899), expandable thumbnail

    Western blot - T-47D whole cell lysate (ab14899)

    The 127 and 37 kDa bands correlate to DDB1 and GAPDH, respectively.

    All lanes: Western blot - Anti-DDB1 with anti-GAPDH internal loading control antibody (Anti-DDB1 with anti-GAPDH internal loading control antibody ab75393) at 1 µg/mL

    Lane 1: HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 2: Hela Whole Cell Lysate - UV Irradiated at 10 µg

    Lane 3: MCF7 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 4: Western blot - T-47D whole cell lysate (ab14899) at 10 µg

    Lane 5: HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 6: Jurkat (Human T cell lymphoblast-like cell line) Whole Cell Lysate at 10 µg

    Lane 7: Caco 2 (Human colonic carcinoma cell line) Whole Cell Lysate at 10 µg

    Secondary

    All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) preadsorbed (Goat Anti-Rabbit IgG H&L (HRP) preadsorbed ab97080) at 1/5000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 127 kDa

    Observed band size: 127 kDa, 32 kDa, 37 kDa, 60 kDa

    Exposure time: 30s

  • Western blot - T-47D whole cell lysate (ab14899), expandable thumbnail

    Western blot - T-47D whole cell lysate (ab14899)

    This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% Milk before being incubated with Anti-YB1 antibody ab12148 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.

    All lanes: Western blot - Anti-YB1 antibody (Anti-YB1 antibody ab12148) at 1 µg/mL

    Lane 1: HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 2: MCF7 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 3: Jurkat (Human) Whole Cell Lysate at 10 µg

    Lane 4: Western blot - T-47D whole cell lysate (ab14899) at 10 µg

    Lane 5: MDA-MB-231 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 10 µg

    Secondary

    All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/50000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 36 kDa

    Observed band size: 100 kDa, 50 kDa

    Exposure time: 4min

  • Western blot - T-47D whole cell lysate (ab14899), expandable thumbnail

    Western blot - T-47D whole cell lysate (ab14899)

    This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with Anti-SGK1 antibody ab43606 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.

    All lanes: Western blot - Anti-SGK1 antibody (Anti-SGK1 antibody ab43606) at 1 µg/mL

    Lane 1: Human BT549 (Breast carcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 2: Western blot - T-47D whole cell lysate (ab14899) at 10 µg

    Lane 3: A431 (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

    Secondary

    All lanes: Goat Anti-Rabbit IgG H&L (HRP) preadsorbed at 1/50000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 48 kDa

    Observed band size: 49 kDa

    Exposure time: 1min

  • Western blot - T-47D whole cell lysate (ab14899), expandable thumbnail

    Western blot - T-47D whole cell lysate (ab14899)

    Wnt9a contains a potential glycosylation site (SwissProt) which may explain its migration at a higher molecular weight than predicted.
    This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 5% Bovine Serum Albumin before being incubated with Anti-Wnt9a antibody ab125957 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution.

    All lanes: Western blot - Anti-Wnt9a antibody (Anti-Wnt9a antibody ab125957) at 1 µg/mL

    Lane 1: Western blot - Mouse lung normal tissue lysate - total protein (Mouse lung normal tissue lysate - total protein ab29297) at 10 µg

    Lane 2: Heart (Mouse) Tissue Lysate at 10 µg

    Lane 3: Western blot - T-47D whole cell lysate (ab14899) at 10 µg

    Lane 4: PANC-1 (Human Pancreatic Carcinoma) Whole Cell Lysate at 10 µg

    Secondary

    All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/10000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 40 kDa

    Observed band size: 110 kDa, 43 kDa, 70 kDa

    Exposure time: 1min

  • Western blot - T-47D whole cell lysate (ab14899), expandable thumbnail

    Western blot - T-47D whole cell lysate (ab14899)

    We hypothesize that the 26 kDa band represents the cleaved form of MUC1. Abcam welcomes customer feedback and would appreciate any comments regarding this product and the data presented above.

    All lanes: Western blot - Anti-MUC1 antibody (Anti-MUC1 antibody ab84597) at 1 µg/mL

    Lane 1: MCF7 (Human breast adenocarcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 2: HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

    Lane 3: Lung (Human) Tissue Lysate at 10 µg

    Lane 4: Western blot - T-47D whole cell lysate (ab14899) at 10 µg

    Secondary

    All lanes: Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 122 kDa

    Observed band size: 24 kDa, 26 kDa

    Exposure time: 2min

  • Western blot - T-47D whole cell lysate (ab14899), expandable thumbnail

    Western blot - T-47D whole cell lysate (ab14899)

    Secondary antibody - anti-rabbit HRP (Goat Anti-Rabbit IgG H&L (HRP) ab6721)

    All lanes: Western blot - Anti-Hsp60 antibody (Anti-Hsp60 antibody ab46798) at 1/50000 dilution

    All lanes: Western blot - T-47D whole cell lysate (ab14899) at 10 µg

    Secondary

    All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab6721) at 1/2000 dilution

    Predicted band size: 61 kDa

    Observed band size: 60 kDa

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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