EI24 Antibodies
We offer EI24 Antibodies for use in common research applications: Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot. Each EI24 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our EI24 Antibodies can be used in a variety of model species: Human. Use the list below to choose the EI24 Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our EI24 polyclonal antibodies.
Alternate Names for EI24 Antibodies
anti-EI24 antibody, anti-EPG4 antibody, anti-etoposide induced 2.4 mRNA antibody, anti-p53-induced gene 8 protein antibody, anti-PIG8etoposide-induced protein 2.4 homolog antibody, anti-TP53I8 antibody, anti-tumor protein p53 inducible protein 8 antibody
7 Results for "ei24" in Primary Antibodies
![Western Blot: EI24 Antibody [NBP2-13949] - Analysis in human cell line HEL.](http://images.novusbio.com/fullsize/EI24-Antibody-Western-Blot-NBP2-13949-img0006.jpg "Western Blot: EI24 Antibody [NBP2-13949] - Analysis in human cell line HEL.")
![Immunocytochemistry/Immunofluorescence: EI24 Antibody [NBP2-13949] - Loss of EI24 expression using CRISPR-Cas9 in MIA PaCa-2 cells decreased cell proliferation. MIA PaCa-2 cells were transfected with CRISPR-Cas9 control (gRNA) and EI24 gRNA (gEI24) using a lentiviral system. After 48 h of incubation, EI24 protein expression was observed by immunofluorescence staining using an anti-EI24 antibody. Image collected and cropped by CiteAb from the following publication (//www.frontiersin.org/article/10.3389/fonc.2019.00652/full), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/EI24-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-13949-img0012.jpg)
![Immunohistochemistry-Paraffin: EI24 Antibody [NBP2-13949] - Staining of human liver shows strong cytoplasmic granular positivity in hepatocytes.](http://images.novusbio.com/fullsize/EI24-Antibody-Immunohistochemistry-Paraffin-NBP2-13949-img0007.jpg)
![Immunohistochemistry-Paraffin: EI24 Antibody [NBP2-13949] - Staining of human parathyroid gland shows strong cytoplasmic granular positivity in glandular cells.](http://images.novusbio.com/fullsize/EI24-Antibody-Immunohistochemistry-Paraffin-NBP2-13949-img0008.jpg)
![Immunohistochemistry-Paraffin: EI24 Antibody [NBP2-13949] - Staining of human prostate shows strong cytoplasmic positivity in smooth muscle cells.](http://images.novusbio.com/fullsize/EI24-Antibody-Immunohistochemistry-Paraffin-NBP2-13949-img0009.jpg)
![Immunohistochemistry-Paraffin: EI24 Antibody [NBP2-13949] - Staining of human pancreas shows strong cytoplasmic granular positivity in exocrine glandular cells.](http://images.novusbio.com/fullsize/EI24-Antibody-Immunohistochemistry-Paraffin-NBP2-13949-img0010.jpg)
![Immunohistochemistry-Paraffin: EI24 Antibody [NBP2-13949] -Staining of human stomach shows strong cytoplasmic granular positivity in glandular cells.](http://images.novusbio.com/fullsize/antibody/nbp2-13949_rabbit-polyclonal-ei24-antibody-immunohistochemistry-paraffin-262023122541..jpg)
![Western Blot: EI24 Antibody [NBP2-13949] - Loss of EI24 expression using CRISPR-Cas9 in MIA PaCa-2 cells decreased cell proliferation. MIA PaCa-2 cells were transfected with CRISPR-Cas9 control (gRNA) & EI24 gRNA (gEI24) using a lentiviral system. (A) After 48 h of incubation, EI24 protein expression was observed by immunofluorescence staining using an anti-EI24 antibody. (B) After 48 h of incubation, the EI24 protein level was observed by western blotting using an anti-EI24 antibody. Conversion of LC3-I to LC3-II & p62 accumulation were analyzed by western blotting using anti-LC3 & anti-p62 antibodies, respectively. Graphs represent the mean ± SEM of EI24, LC3-II, & p62 densitometry value to that of beta -actin (with gRNA values set to 1) from three independent experiments. Comparison were made using Student's t-test, *P < 0.05; **P < 0.01; ***P < 0.001. (C) After 24 h of incubation, cells were seeded into a 96-well plate (1,000 cells/well). Images acquired by the IncuCyte instrument at the indicated times were analyzed using the ZOOM 2016 program. Confluency was measured in triplicate wells for each sample. Values represent the means ± SEM (Student's t-test, *P < 0.05; **P < 0.01; ***P < 0.001). (D) Control & EI24 gRNA-transfected cells (5 × 106) were injected into both flanks of Balb/c nude mice. Tumor volume was measured on the indicated days. The y-axes of these graphs represent the fold change in tumor size relative to the initial tumor size. Values represent means ± SEM. (Student's t-test, n.s., not significant, control gRNA mice, n = 5; EI24 gRNA mice, n = 4). Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31396480), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nbp2-13949_rabbit-polyclonal-ei24-antibody-310202416113540.jpg)
![Western Blot: EI24 Antibody [NBP2-13949] - Loss of EI24 expression in HCT116 cells impairs autophagy but not cell proliferation. HCT116 cells were transfected with 10 nM control siRNA (siCtrl) or siRNA targeting EI24 or ATG5. (A) The mRNA levels of EI24, ATG5, & GAPDH were analyzed by reverse-transcription PCR. (B) The protein levels of EI24 ATG5 & beta -actin were analyzed by western blotting. Representative data are shown. Values represent the ratio of the EI24 or ATG5 densitometry value to that of beta -actin (with siCtrl values set to 1). Conversion of LC3-I to LC3-II & p62 accumulation were analyzed by western blotting using anti-LC3 & anti-p62 antibodies, respectively. Graphs represent mean ± SEM of the LC3-II & p62 densitometry value to that of beta -actin (with siCtrl values set to 1) from three independent experiments. Comparison were made using Student's t-test, *P < 0.05; **P < 0.01. (C) After 24 h of transfection, cells were seeded into a 6-well plate & incubated for another 7 days. Cells were fixed & stained with crystal violet. (D) After 24 h of transfection, cells were seeded into a 96-well plate. Images acquired from the IncuCyte instrument at the indicated times were analyzed using the ZOOM 2016 program. Cell confluency was measured in triplicate wells for each sample. The plotted values represent means ± SEM. (E) Protein extracts from siRNA-transfected cells were analyzed for DNA fragmentation. The y-axes of the graphs indicate the extent of DNA fragmentation. Values plotted in the graphs represent means ± SEM (Student's t-test, n.s., not significant). Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31396480), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nbp2-13949_rabbit-polyclonal-ei24-antibody-310202416121988.jpg)
![Western Blot: EI24 Antibody [NBP2-81820] - Analysis of EI24 in rat liver tissue lysate with EI24 antibody at (A) 1 and (B) 2 ug/ml.](http://images.novusbio.com/fullsize/EI24-Antibody-Western-Blot-NBP2-81820-img0001.jpg "Western Blot: EI24 Antibody [NBP2-81820] - Analysis of EI24 in rat liver tissue lysate with EI24 antibody at (A) 1 and (B) 2 ug/ml.")
![Immunohistochemistry: EI24 Antibody - BSA Free [NBP2-81820] - Immunohistochemistry of EI24 in rat liver tissue with EI24 antibody at 5 ug/mL.](http://images.novusbio.com/fullsize/nbp2-81820_rabbit-polyclonal-ei24-antibody-271120242041452.jpg)
![Western Blot: EI24 Antibody [NBP2-48993] - Analysis in control (vector only transfected HEK293T lysate) and EI24 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).](http://images.novusbio.com/fullsize/EI24-Antibody-Western-Blot-NBP2-48993-img0006.jpg "Western Blot: EI24 Antibody [NBP2-48993] - Analysis in control (vector only transfected HEK293T lysate) and EI24 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).")
![Immunocytochemistry/Immunofluorescence: EI24 Antibody [NBP2-48993] - Staining of human cell line U-2 OS shows localization to cytosol & endoplasmic reticulum. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/EI24-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-48993-img0005.jpg)
![Western Blot: EI24 Antibody - BSA Free [NBP3-46592] - HeLa cells were subjected to SDS PAGE followed by western blot with (EI24 antibody) at dilution of 1:600](http://images.novusbio.com/fullsize/nbp3-46592_rabbit-ei24-pab-bsa-free-284202511463151.jpg "Western Blot: EI24 Antibody - BSA Free [NBP3-46592] - HeLa cells were subjected to SDS PAGE followed by western blot with (EI24 antibody) at dilution of 1:600")
![Western Blot: EI24 Antibody [NBP1-98605] - Hela Cell Lysate 1.0ug/ml, Gel Concentration: 12%](http://images.novusbio.com/fullsize/EI24-Antibody-Western-Blot-NBP1-98605-img0002.jpg "Western Blot: EI24 Antibody [NBP1-98605] - Hela Cell Lysate 1.0ug/ml, Gel Concentration: 12%")
![Immunoprecipitation:[NBP3-18376]-Detection of human EI24 by western blot of immunoprecipitates. Samples: Whole cell lysate from Jurkat cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-EI24 antibody used for IP at 6 µg per reaction. EI24 was also immunoprecipitated by rabbit anti-EI24 antibody. For blotting immunoprecipitated EI24, was used at 0. 4 mg/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/nbp3-18376_rabbit-ei24-pab-231202512101652.jpg "Immunoprecipitation:[NBP3-18376]-Detection of human EI24 by western blot of immunoprecipitates. Samples: Whole cell lysate from Jurkat cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-EI24 antibody used for IP at 6 µg per reaction. EI24 was also immunoprecipitated by rabbit anti-EI24 antibody. For blotting immunoprecipitated EI24, was used at 0. 4 mg/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")