Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric)

8 product images

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  Western blot - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  Blocking and diluting buffer: 5% NFDM/TBST.
  

  Exposure time: Lane 1: 30 seconds
  Lane 2: 70 seconds
  Lane 3: 50 seconds
  

  All lanes: Western blot - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826) at 1/1000 dilution

  Lane 1: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 15 µg

  Lane 2: NIH/3T3 (Mouse embryonic fibroblast) whole cell lysates at 15 µg

  Lane 3: PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysates at 15 µg

  Secondary

  All lanes: Western blot - Rabbit Anti-Mouse IgG H&L (HRP) (Rabbit Anti-Mouse IgG H&L (HRP) ab6728) at 1/2000 dilution

  Predicted band size: 44 kDa

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  Flow Cytometry (Intracellular) - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  ab210826 staining TXNIP in HeLa (Human cervix adenocarcinoma epithelial cell line) by intracellular flow cytometry. Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. The sample was incubated with primary antibody at 1/100 dilution (1μg/ml) (red). An Alexa Fluor^® 488 Goat anti mouse IgG (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113) was used at 1/2000 dilution. Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) was used as isotype control (black). Cell without incubation with primary antibody and secondary antibody (blue).
  

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  Immunocytochemistry/ Immunofluorescence - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  ab210826 staining TXNIP in 293T (human embryonic kidney epithelial cell line) cells by Immunocytochemistry/Immunofluorescence (ICC/IF). The cells were fixed with 100% Methanol. Samples were incubated with primary antibody at 10μg/ml (1:100 dilution). An Alexa Fluor^® 488 Goat Anti-Mouse was used as the secondary antibody at 2μg/ml (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113). Anti-beta IV Tubulin antibody [EPR16775] ab179504, Anti-beta IV Tubulin was used as a counterstain at 2μg/ml and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor^® 594) was used as secondary antibody counterstain at 4μg/ml.
  For negative control 1, primary antibody was used at a 10μg/ml and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080 was used as secondary antibody at 4 μg/ml. For negative control 2, Anti-beta IV Tubulin antibody [EPR16775] ab179504 was used as a primary antibody at 2μg/ml and Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113 was used as a secondary antibody at 2 μg/ml. DAPI was used as a nuclear counterstain. Confocal image showing cytoplasmic staining in 293T cells.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  IHC image of TxNIP staining in a section of formalin fixed, paraffin embedded human normal kidney tissue section*, performed on a Leica Bond™ system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab210826, 2μg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
  

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre

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  Immunocytochemistry/ Immunofluorescence - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  ab210826 stained in NIH3T3 cells. The cells were fixed with 100% methanol (5min) at room temperature and incubated with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% triton for 1h at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab210826 at 5μg/ml overnight at +4°C. The secondary antibody was Donkey Anti-Sheep IgG H&L (Alexa Fluor® 488) ab150177 used at 1 ug/ml for 1hour at room temperature (colored green). Alexa Fluor® 594 Anti-beta Tubulin antibody [EPR16774] - Microtubule Marker ab206369 (Rabbit monoclonal [EPR16774] to beta Tubulin Alexa Fluor® 594) was used as a counterstaining at a 1/200 dilution for 1hour at room temperature (pseudo-colored red). DAPI was used to stain the cell nuclei (colored blue) at a concentration of 1.43μM for 1hour at room temperature.

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  Western blot - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  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 (LANE 1) and 2% Bovine Serum Albumin (lane 2) before being incubated with ab210826 (lane 1) and Anti-TXNIP antibody [EPR14774] ab188865 (lane 2) overnight at 4°C. Antibody binding was detected using an anti-mouse (lane 1) and anti-rabbit (lane 2) antibody conjugated to HRP, and visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.

  All lanes: Western blot - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826) at 5 µg

  All lanes: HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate at 10 µg

  Secondary

  Lane 1: Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/5000 dilution

  Lane 2: Peroxidase AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/50000 dilution

  Developed using the ECL technique.

  Performed under reducing conditions.

  Predicted band size: 44 kDa

  Observed band size: 55 kDa

  Exposure time: 16min

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  IHC image of ab210826 staining in a section of formalin fixed, paraffin embedded mouse normal kidney, using MOM detection kit, ab127055. The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH6) for 30mins. The section was incubated with ab210826, 2μg/ml, for 15 mins at room temperature. DAB was used as the chromogen (ab103723), diluted 1/100 and incubated for 10min at room temperature. The section was counterstained with haematoxylin and mounted with DPX.
  

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunocytochemistry/ Immunofluorescence - Anti-TXNIP antibody [EPR14774] - Mouse IgG2b (Chimeric) (ab210826)

  ab210826 stained in Hela cells. The cells were fixed with 100% methanol (5min) at room temperature and incubated with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% triton for 1h at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab210826 at 5μg/ml overnight at +4°C. The secondary antibody was Donkey Anti-Sheep IgG H&L (Alexa Fluor® 488) ab150177 used at 1 ug/ml for 1hour at room temperature (colored green). Alexa Fluor® 594 Anti-beta Tubulin antibody [EPR16774] - Microtubule Marker ab206369 (Rabbit monoclonal [EPR16774] to beta Tubulin Alexa Fluor® 594) was used as a counterstaining at a 1/200 dilution for 1hour at room temperature (pseudo-colored red). DAPI was used to stain the cell nuclei (colored blue) at a concentration of 1.43μM for 1hour at room temperature.