Anti-SP1 antibody [EPR6662(B)]

13 product images

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  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Lanes 1-2: Merged signal (red and green). Green - ab124804 observed at 100 kDa. Red - loading control Anti-GAPDH antibody [6C5] - Loading Control ab8245 observed at 37 kDa.
  

  ab124804 Anti-SP1 antibody [EPR6662(B)] was shown to specifically react with SP1 in wild-type HeLa cells. Loss of signal was observed when knockout cell line Human SP1 knockout HeLa cell line ab265519 (knockout cell lysate Human SP1 knockout HeLa cell lysate ab257698) was used. Wild-type and SP1 knockout samples were subjected to SDS-PAGE. ab124804 and Anti-GAPDH antibody [6C5] - Loading Control (Anti-GAPDH antibody [6C5] - Loading Control ab8245) were incubated overnight at 4°C at 1 in 5000 and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804) at 1/5000 dilution

  Lane 1: Wild-type HeLa cell lysate at 20 µg

  Lane 2: SP1 knockout HeLa cell lysate at 20 µg

  Lane 2: Western blot - Human SP1 knockout HeLa cell line (Human SP1 knockout HeLa cell line ab265519)

  Performed under reducing conditions.

  Predicted band size: 81 kDa

  Observed band size: 100 kDa

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  Flow Cytometry (Intracellular) - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Intracellular Flow Cytometry analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling SP1 with Purified ab124804 at 1/100 dilution (10 μg/ml) (Red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor^® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody was used at 1/2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).

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  Immunocytochemistry/ Immunofluorescence - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Immunocytochemistry/ Immunofluorescence analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling SP1 with Purified ab124804 at 1:200 dilution (4 µg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with None. Goat anti rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) was used as the secondary antibody at 1:1000 (2 µg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human gastric carcinoma tissue sections labeling SP1 with Purified ab124804 at 1:2000 dilution (0.41 µg/ml). Perform heat mediated antigen retrieval using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). Purified)ImmunoHistoProbe one step HRP Polymer (ready to use) was used for detection. Negative control: PBS instead of the primary antibody. Hematoxylin was used as a counterstain.

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  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  We are unsure how to define the extra bands.

  All lanes: Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804) at 1/5000 dilution

  All lanes: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 20 µg

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution

  Predicted band size: 81 kDa

  Observed band size: 100 kDa

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  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  We are unsure how to define the extra bands.

  All lanes: Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804) at 1/5000 dilution

  All lanes: Ramos (Human Burkitt's lymphoma B lymphocyte) whole cell lysates at 15 µg

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution

  Predicted band size: 81 kDa

  Observed band size: 100 kDa

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  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Lanes 1 - 4: Merged signal (red and green). Green - ab124804 observed at 100 kDa. Red - loading control, Anti-GAPDH antibody [6C5] - Loading Control ab8245, observed at 37 kDa.
  

  Anti-HDAC2 antibody ab16032 detected the expected band for SP1 in wild-type HAP1 cells along with additional cross-reactive bands. The band was not seen in SP1 knockout HAP1 cells. Wild-type and SP1 knockout samples were subjected to SDS-PAGE. ab124804 and Anti-GAPDH antibody [6C5] - Loading Control ab8245 (loading control to GAPDH) were diluted 1/1000 and 1/2000 respectively and incubated overnight at 4°C. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776) secondary antibodies at 1/10000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804) at 1/1000 dilution

  Lane 1: Wild-type HAP1 cell lysate at 20 µg

  Lane 2: SP1 knockout HAP1 cell lysate at 20 µg

  Lane 3: HeLa cell lysate at 20 µg

  Lane 4: K562 cell lysate at 20 µg

  Predicted band size: 81 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  ab124804, at 1/100 dilution staining SP1 in paraffin-embedded Human colon tissue, by Immunohistochemistry.
  

  Perform heat mediated antigen retrieval before commencing with IHC staining protocol.

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  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Lanes 1 - 4: Merged signal (red and green). Green - ab124804 observed at 100 kDa. Red - loading control, Anti-GAPDH antibody [6C5] - Loading Control ab8245, observed at 37 kDa.
  

  This western blot image is a comparison between ab124804 and a competitor's top cited rabbit polyclonal antibody.

  All lanes: Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  Lane 1: Wild-type HAP1 cell lysate at 20 µg

  Lane 2: SP1 knockout HAP1 cell lysate at 20 µg

  Lane 3: HeLa cell lysate at 20 µg

  Lane 4: K562 cell lysate at 20 µg

  Predicted band size: 81 kDa

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  OI-RD Scanning - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody.
  Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.

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  ChIC/CUT&RUN sequencing - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  ChIC/CUT&RUN was performed using a pAG-MNAse at a final concentration of 700 ng/mL. 2.5X10^5 of Human wild-type HeLa cell line (ab255928) or Human SP1 knockout HeLa cell line (Human SP1 knockout HeLa cell line ab265519) were used along with 5µg of ab124804 [EPR6662(B)]. Assay Quality Control was conducted using 5µg Anti-CTCF (Anti-CTCF antibody [EPR18253] - ChIP Grade ab188408) on the same cell lines. The resulting DNA was sequenced on the Illumina NovaSeq 6000 to a depth of 10 million reads.? The negative IgG control Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730 is also shown.
  
  Additional screenshots of mapped reads can be found in the Protocol booklet in the Support and downloads section.
  
  The University of Geneva owns patents relevant to ChIC (Chromatin Immuno-Cleavage) methods.

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  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  SP1 Western blot staining using rabbit Anti-SP1 antibody

  Western blot: Rabbit Monoclonal[EPR6662(B)] to SP1 ab124804 staining at 1/1000 dilution, shown in green; Mouse anti GAPDH (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20,000 dilution, shown in magenta. A band was observed at 90 kDa in Wild-type MCF7 cell lysates with no signal observed at this size in SP1 knockout MCF7 cell line. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.

  All lanes: Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804) at 1/1000 dilution

  Lane 1: Wild-type MCF7 at 20 µg

  Lane 2: SP1 knockout MCF7 at 20 µg

  Lane 2: Western blot - Human SP1 knockout MCF7 cell line (ab287770) at 20 µg

  Lane 3: HeLa at 20 µg

  Lane 4: Ramos at 20 µg

  Secondary

  All lanes: Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution

  Performed under reducing conditions.

  Predicted band size: 81 kDa

  Observed band size: 90 kDa

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  Image collected and cropped by CiteAb under a CC-BY license from the publication

  Western blot - Anti-SP1 antibody [EPR6662(B)] (ab124804)

  SP1 western blot using anti-SP1 antibody [EPR6662(B)] ab124804. Publication image and figure legend from Shi, M., An, G., et al., 2023, Cancers (Basel), PubMed 37173968.

  
  

  ab124804 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab124804 please see the product overview.

  Correlation between UVRAG expression and therapeutic resistance. (A) Relative expression of UVRAG in HCT8, HCT8-5Fu, and HCT8-60Gy cells. (B) The sensitivity of HCT8-CON and HCT8-UVRAG cells to radiotherapy. (C) UVRAG knockdown increased 5-Fu sensitivity. (D) UVRAG overexpression decreased 5-Fu sensitivity. (E) Relative mRNA expression of UVRAG in HCT116 and HCT116-self cells. (F) Relative mRNA expression of UVRAG in HCT116 DCLK- and HCT116 DCLK+ cells. (G) Western blot of PD-L1, UVARG, ABCG2, BMI1, and SP1 after upregulating UVARG or downregulating UVRAG. The uncropped blots are shown in Figure S1. (H) Spheroid formation in UVRAG overexpressed HCT116 and its control cells. (I) Stem cell score evaluated via ssGSEA in patients with UVRAG higher expression and UVARG lower expression. Independent-samples t-test (A,E,F). Mann Whitney U test (I). * p < 0.05, ** p < 0.01.