Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free

8 product images

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  ChIP - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  Chromatin was prepared from NCCIT cells according to the Abcam Dual-X-ChIP protocol. Cells were fixed with 1.5 mM EGS for 30mins and then 1% formaldehyde for 10min.
  

  The ChIP was performed with 25 μg of chromatin, 2 μg of Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 (red), or 2 μg of rabbit normal IgG Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730 (gray) and 20 μl of Protein A/G sepharose beads. The immunoprecipitated DNA was quantified by real time PCR (Taqman approach for active and inactive loci, Sybr green approach for heterochromatic loci).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

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  Western blot - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  False colour image of Western blot: Anti-CBX4 antibody [EPR23053-7] - ChIP Grade staining at 1/1000 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291) loading control staining at 1/20000 dilution, shown in red. In Western blot, Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 was shown to bind specifically to CBX4. A band was observed at 75 kDa in wild-type HEK-293 cell lysates with no signal observed at this size in Cbx4 CRISPR-Cas9 edited cell line Human CBX4 knockout HEK-293 cell line ab261723 (CRISPR-Cas9 edited cell lysate ab261666). The band observed in the CRISPR-Cas9 edited lysate lane below 75 kDa is likely to represent a truncated form of CBX4. This has not been investigated further and the functional properties of the gene product have not been determined. To generate this image, wild-type and Cbx4 CRISPR-Cas9 edited HEK-293 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween^® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) at 1/20000 dilution.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

  All lanes: Western blot - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149) at 1/1000 dilution

  Lane 1: Wild-type HEK-293 cell lysate at 20 µg

  Lane 2: Cbx4 CRISPR-Cas9 edited HEK-293 cell lysate at 20 µg

  Lane 2: Western blot - Human CBX4 knockout HEK-293 cell line (Human CBX4 knockout HEK-293 cell line ab261723)

  Lane 3: RAW 264.7 cell lysate at 20 µg

  Lane 4: HUVEC cell lysate at 20 µg

  Performed under reducing conditions.

  Predicted band size: 61 kDa

  Observed band size: 75 kDa

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  Immunoprecipitation - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  CBX4 was immunoprecipitated from 0.35 mg HCT 116 (Human colorectal carcinoma epithelial cell) whole cell lysate with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
  

  Lane 1: HCT 116 (Human colorectal carcinoma epithelial cell) whole cell lysate 10ug

  Lane 2: Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 IP in HCT 116 whole cell lysate

  Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 in HCT 116 whole cell lysate

  Blocking and dilution buffer and concentration: 5% NFDM/TBST.

  Exposure time: 15 seconds.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

  All lanes: Immunoprecipitation - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149)

  Predicted band size: 52 kDa, 61 kDa

  Observed band size: 45 kDa, 60 kDa, 66 kDa, 74 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  Immunohistochemical analysis of paraffin-embedded Rat hippocampus tissue labeling CBX4 with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/200 dilution (2.785 ug/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP Polymer). Nuclear staining on rat hippocampus (PMID: 28283560). The section was incubated with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 for 30 at RT. The immunostaining staining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with Hematoxylin.
  

  Secondary antibody only control: Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP Polymer).

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

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  Flow Cytometry (Intracellular) - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  Intracellular flow cytometric analysis of 4% paraformaldehyde fixed, 90% methanol permeabilized NCCIT (Human pluripotent embryonic carcinoma epithelial cell) cells labelling CBX4 with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/600 dilution (Red) compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor^®488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  Immunohistochemical analysis of paraffin-embedded Mouse hippocampus tissue labeling CBX4 with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/200 dilution (2.785 ug/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP Polymer). Nuclear staining on mouse hippocampus (PMID: 28283560). The section was incubated with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 for 30 at RT. The immunostaining staining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with Hematoxylin.
  

  Secondary antibody only control: Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP Polymer).

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling CBX4 with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/200 dilution (2.785 ug/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP Polymer). Nuclear staining on mouse cerebrum (PMID: 28283560). The section was incubated with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 for 30 mins at RT. The immunostaining staining was performed on a Leica Biosystems BOND^® RX instrument. Counterstained with Hematoxylin.
  

  Secondary antibody only control: Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP Polymer).

  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).

• 

  Flow Cytometry (Intracellular) - Anti-CBX4 antibody [EPR23053-7] - ChIP Grade - BSA and Azide free (ab269462)

  Intracellular flow cytometric analysis of 4% paraformaldehyde fixed, 90% methanol permeabilized HCT 116 (Human colorectal carcinoma epithelial cell) cells labelling CBX4 with Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149 at 1/600 dilution (Red) compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor^®488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/2000 dilution was used as the secondary antibody.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CBX4 antibody [EPR23053-7] - ChIP Grade ab242149).