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![Western Blot: EBOV VP35 protein Antibody [NBP3-13340] - Non-transfected (-) and transfected (+) 293T whole cell extracts (5 ug) were separated by 10% SDS-PAGE, and the membranes were blotted with EBOV VP35 protein antibody (NBP3-13340) diluted at 1:5000 and DDDDK tag antibody (NBP2-43574) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-VP35-protein-Antibody-Western-Blot-NBP3-13340-img0001.jpg "Western Blot: EBOV VP35 protein Antibody [NBP3-13340] - Non-transfected (-) and transfected (+) 293T whole cell extracts (5 ug) were separated by 10% SDS-PAGE, and the membranes were blotted with EBOV VP35 protein antibody (NBP3-13340) diluted at 1:5000 and DDDDK tag antibody (NBP2-43574) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: EBOV VP35 protein Antibody [NBP3-13340] - EBOV VP35 protein antibody detects EBOV VP35 protein protein at cytoplasm by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: EBOV VP35 protein protein stained by EBOV VP35 protein antibody (NBP3-13340) diluted at 1:1000. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/EBOV-VP35-protein-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13340-img0002.jpg)
![Western Blot: EBOV VP30 protein Antibody [NBP3-13345] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with EBOV VP30 protein antibody (NBP3-13345) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-VP30-protein-Antibody-Western-Blot-NBP3-13345-img0001.jpg "Western Blot: EBOV VP30 protein Antibody [NBP3-13345] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with EBOV VP30 protein antibody (NBP3-13345) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: EBOV VP30 protein Antibody [NBP3-13345] - EBOV VP30 protein antibody detects EBOV VP30 protein protein at cytoplasm by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: EBOV VP30 protein protein stained by EBOV VP30 protein antibody (NBP3-13345) diluted at 1:1000. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/EBOV-VP30-protein-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13345-img0002.jpg)
![Western Blot: EBOV GP1 Antibody [NBP3-13370] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EBOV GP1 antibody (NBP3-13370) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-GP1-Antibody-Western-Blot-NBP3-13370-img0001.jpg "Western Blot: EBOV GP1 Antibody [NBP3-13370] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EBOV GP1 antibody (NBP3-13370) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: EBOV GP1 Antibody [NBP3-13370] - EBOV GP1 antibody detects EBOV GP1 protein at cytoplasm by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: EBOV GP1 protein stained by EBOV GP1 antibody (NBP3-13370) diluted at 1:1000. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/EBOV-GP1-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13370-img0002.jpg)
![Western Blot: EBOV VP30 protein Antibody [NBP3-13344] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP30 protein antibody (NBP3-13344) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-VP30-protein-Antibody-Western-Blot-NBP3-13344-img0001.jpg "Western Blot: EBOV VP30 protein Antibody [NBP3-13344] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP30 protein antibody (NBP3-13344) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: EBOV VP30 protein Antibody [NBP3-13344] - EBOV VP30 protein antibody detects EBOV VP30 protein protein at cytoplasm by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: EBOV VP30 protein protein stained by EBOV VP30 protein antibody (NBP3-13344) diluted at 1:1000. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/EBOV-VP30-protein-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13344-img0002.jpg)
![Western Blot: EBOV VP40 protein Antibody [NBP3-13342] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP40 protein antibody (NBP3-13342) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-VP40-protein-Antibody-Western-Blot-NBP3-13342-img0001.jpg "Western Blot: EBOV VP40 protein Antibody [NBP3-13342] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP40 protein antibody (NBP3-13342) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: EBOV VP40 protein Antibody [NBP3-13342] - EBOV VP40 protein antibody detects EBOV VP40 protein protein at cytoplasm by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: EBOV VP40 protein protein stained by EBOV VP40 protein antibody (NBP3-13342) diluted at 1:1000. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/EBOV-VP40-protein-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13342-img0002.jpg)
![Western Blot: EBOV GP2-delta Antibody [NBP3-13371] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EBOV GP2-delta antibody (NBP3-13371) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-GP2-delta-Antibody-Western-Blot-NBP3-13371-img0001.jpg "Western Blot: EBOV GP2-delta Antibody [NBP3-13371] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EBOV GP2-delta antibody (NBP3-13371) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Immunocytochemistry/Immunofluorescence: EBOV GP2-delta Antibody [NBP3-13371] - EBOV GP2-delta antibody detects EBOV GP2-delta protein at cytoplasm by immunofluorescent analysis. Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: EBOV GP2-delta protein stained by EBOV GP2-delta antibody (NBP3-13371) diluted at 1:500. Blue: Hoechst 33342 staining. Scale bar = 10 um.](http://images.novusbio.com/fullsize/EBOV-GP2-delta-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-13371-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: EBOV Antibody [NBP3-14861] - Hela cells were transfected with plasmids expressing Ebola Zaire glycoprotein, nucleoprotein or VP40, seeded on coverslips and incubated for 48 h. Control coverslips consisted of untransfected cells. After fixation with 4% PFA, samples were stained with EBOV antibody. Antibody was used at a dilution of 1:500 and Triton X-100 was used as detergent. Imaging was performed using a Leica SP5 confocal microscope (Images by Virology Research Services Ltd).](http://images.novusbio.com/fullsize/EBOV-Antibody-Immunocytochemistry-Immunofluorescence-NBP3-14861-img0001.jpg "Immunocytochemistry/Immunofluorescence: EBOV Antibody [NBP3-14861] - Hela cells were transfected with plasmids expressing Ebola Zaire glycoprotein, nucleoprotein or VP40, seeded on coverslips and incubated for 48 h. Control coverslips consisted of untransfected cells. After fixation with 4% PFA, samples were stained with EBOV antibody. Antibody was used at a dilution of 1:500 and Triton X-100 was used as detergent. Imaging was performed using a Leica SP5 confocal microscope (Images by Virology Research Services Ltd).")
![Western Blot: EBOV Nucleoprotein Antibody [NBP3-13339] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EBOV Nucleoprotein antibody (NBP3-13339) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-Nucleoprotein-Antibody-Western-Blot-NBP3-13339-img0001.jpg "Western Blot: EBOV Nucleoprotein Antibody [NBP3-13339] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EBOV Nucleoprotein antibody (NBP3-13339) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: EBOV VP30 protein Antibody [NBP3-13343] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP30 protein antibody (NBP3-13343) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-VP30-protein-Antibody-Western-Blot-NBP3-13343-img0001.jpg "Western Blot: EBOV VP30 protein Antibody [NBP3-13343] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP30 protein antibody (NBP3-13343) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: EBOV VP35 protein Antibody [NBP3-13341] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP35 protein antibody (NBP3-13341) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/EBOV-VP35-protein-Antibody-Western-Blot-NBP3-13341-img0001.jpg "Western Blot: EBOV VP35 protein Antibody [NBP3-13341] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with EBOV VP35 protein antibody (NBP3-13341) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![Western Blot: EBOV VP40 protein Antibody (02) [NBP3-12761] - Ebola virus EBOV (subtype Sudan, strain Gulu) VP40 Recombinant Protein Lane A: 30ng Lane B: 10ng Secondary Goat Anti-Mouse IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions.](http://images.novusbio.com/fullsize/EBOV-VP40-protein-Antibody-02-Western-Blot-NBP3-12761-img0001.jpg "Western Blot: EBOV VP40 protein Antibody (02) [NBP3-12761] - Ebola virus EBOV (subtype Sudan, strain Gulu) VP40 Recombinant Protein Lane A: 30ng Lane B: 10ng Secondary Goat Anti-Mouse IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions.")
![Western Blot: EBOV Nucleoprotein Antibody (09) [NBP3-12759] - Ebola virus EBOV (subtype Zaire, strain H.sapiens-wt/GIN/2014/Kissidougou-C15) Nucleoprotein / NP ProteinLane A: 30ngSecondaryGoat Anti-Mouse IgG (H+L)/HRP at 1/10000 dilutionDeveloped using the ECL technique.Performed under reducing conditions.](http://images.novusbio.com/fullsize/EBOV-Nucleoprotein-Antibody-09-Western-Blot-NBP3-12759-img0001.jpg "Western Blot: EBOV Nucleoprotein Antibody (09) [NBP3-12759] - Ebola virus EBOV (subtype Zaire, strain H.sapiens-wt/GIN/2014/Kissidougou-C15) Nucleoprotein / NP ProteinLane A: 30ngSecondaryGoat Anti-Mouse IgG (H+L)/HRP at 1/10000 dilutionDeveloped using the ECL technique.Performed under reducing conditions.")