| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21185-100ul | |||
| BSA Free | NBP3-21185-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-05384-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-59432-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-93004-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98989-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98742-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81118-0.025mg | |||
![Western Blot: NEDD1 Antibody [NB100-55420] - (0.1ug/ml) staining of HeLa cell lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/NEDD1-Antibody-Western-Blot-NB100-55420-img0002.jpg "Western Blot: NEDD1 Antibody [NB100-55420] - (0.1ug/ml) staining of HeLa cell lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")
![Western Blot: SESN2 Antibody (8I1W4) [NBP3-33447] - Western blot analysis of various lysates, using SESN2 Rabbit mAb at 1:2000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 3s.](http://images.novusbio.com/fullsize/nbp3-33447_rabbit-sesn2-mab-8i1w4-1012202411381237.jpg "Western Blot: SESN2 Antibody (8I1W4) [NBP3-33447] - Western blot analysis of various lysates, using SESN2 Rabbit mAb at 1:2000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 3s.")
![Western Blot: SESN2 Antibody (8I1W4) [NBP3-33447] - Western blot analysis of various lysates, using SESN2 Rabbit mAb at 1:2000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 60s.](http://images.novusbio.com/fullsize/nbp3-33447_rabbit-sesn2-mab-8i1w4-1012202411334039.jpg)
![Western Blot: MDM2/HDM2 [p Ser166] Antibody [NBP3-05384] - Western blot analysis of extracts of 293 cells, using MDM2/HDM2 antibody (NBP3-05384). 293 cells were treated by Hydroxyurea (4mM) for 20 hours. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA.](http://images.novusbio.com/fullsize/MDM2-HDM2-[p-Ser166]-Antibody-Western-Blot-NBP3-05384-img0002.jpg "Western Blot: MDM2/HDM2 [p Ser166] Antibody [NBP3-05384] - Western blot analysis of extracts of 293 cells, using MDM2/HDM2 antibody (NBP3-05384). 293 cells were treated by Hydroxyurea (4mM) for 20 hours. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA.")
![Immunocytochemistry/ Immunofluorescence: MDM2/HDM2 [p Ser166] Antibody - BSA Free [MDM2/HDM2] - Immunofluorescence analysis of paraffin-embedded Human breast cancer tissue using MDM2/HDM2 Rabbit pAb at a dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining. Perform high pressure antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining.](http://images.novusbio.com/fullsize/nbp3-05384_rabbit-polyclonal-mdm2-hdm2-p-ser166-antibody-5220251640233.jpg)
![Western Blot: AIF Antibody (22E9) [NBP2-59432] - Lane 1: Mouse heart tissue lysates, Lane 2: Mouse liver tissue lysates](http://images.novusbio.com/fullsize/AIF-AIFM1-Antibody-22E9-Western-Blot-NBP2-59432-img0001.jpg "Western Blot: AIF Antibody (22E9) [NBP2-59432] - Lane 1: Mouse heart tissue lysates, Lane 2: Mouse liver tissue lysates")
![Immunocytochemistry/Immunofluorescence: AIF Antibody (22E9) [NBP2-59432] - Analysis of AIFM1 in Hep3B cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human AIFM1 antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).](http://images.novusbio.com/fullsize/AIF-AIFM1-Antibody-22E9-Immunocytochemistry-Immunofluorescence-NBP2-59432-img0002.jpg)
![Western Blot: MDA5 Antibody (2N8Z5) [NBP3-16132] - Analysis of extracts of various cell lines, using MDA5 antibody (NBP3-16132) at 1:1000 dilution.C6 cells were treated by LPS for 6 hours and Brefeldin A for 3 hours of stimulation. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 10s.](http://images.novusbio.com/fullsize/MDA5-Antibody-2N8Z5-Western-Blot-NBP3-16132-img0001.jpg "Western Blot: MDA5 Antibody (2N8Z5) [NBP3-16132] - Analysis of extracts of various cell lines, using MDA5 antibody (NBP3-16132) at 1:1000 dilution.C6 cells were treated by LPS for 6 hours and Brefeldin A for 3 hours of stimulation. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 10s.")
![Western Blot: MDA5 Antibody (2N8Z5) [NBP3-16132] - Analysis of extracts of BxPC-3 cells, using MDA5 antibody (NBP3-16132) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 90s.](http://images.novusbio.com/fullsize/MDA5-Antibody-2N8Z5-Western-Blot-NBP3-16132-img0002.jpg)
![Western Blot: CHAF1B Antibody (7N0I2) [NBP3-16545] - Western blot analysis of extracts of various cell lines, using CHAF1B Rabbit mAb (NBP3-16545) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.](http://images.novusbio.com/fullsize/CHAF1B-Antibody-7N0I2-Western-Blot-NBP3-16545-img0002.jpg "Western Blot: CHAF1B Antibody (7N0I2) [NBP3-16545] - Western blot analysis of extracts of various cell lines, using CHAF1B Rabbit mAb (NBP3-16545) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 1s.")
![Immunohistochemistry-Paraffin: CHAF1B Antibody (7N0I2) [NBP3-16545] - Immunohistochemistry of paraffin-embedded human colon carcinoma using CHAF1B Rabbit mAb (NBP3-16545) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/CHAF1B-Antibody-7N0I2-Immunohistochemistry-Paraffin-NBP3-16545-img0001.jpg)
![Western Blot: NOX5 Antibody [NBP2-93004] - Western blot analysis of extracts of PC-3 cells, using NOX5 antibody (NBP2-93004) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s.](http://images.novusbio.com/fullsize/NOX5 Antibody-Western Blot-NBP2-93004-img0002.jpg "Western Blot: NOX5 Antibody [NBP2-93004] - Western blot analysis of extracts of PC-3 cells, using NOX5 antibody (NBP2-93004) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 180s.")
![Immunocytochemistry/ Immunofluorescence: NOX5 Antibody - Azide and BSA Free [NBP2-93004] - Immunofluorescence analysis of A-549 cells using NOX5 Rabbit pAb at dilution of 1:100 (40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp2-93004_rabbit-polyclonal-nox5-antibody-42202514264489.jpg)
![Immunohistochemistry-Paraffin: Cdk3 Antibody [NBP2-98989] - Immunochemical staining of human Cdk3 in human testis with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/Cdk3-Antibody-Immunohistochemistry-Paraffin-NBP2-98989-img0002.jpg "Immunohistochemistry-Paraffin: Cdk3 Antibody [NBP2-98989] - Immunochemical staining of human Cdk3 in human testis with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).")
![Immunocytochemistry/Immunofluorescence: Cdk3 Antibody [NBP2-98989] - Immunofluorescence staining of Cdk3 in U251MG cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98989 antibody (dilution ratio 1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor$488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-98989_rabbit-polyclonal-cdk3-antibody-235202511444415.png)
![Immunohistochemistry-Paraffin: GADD153/CHOP Antibody [NBP2-98742] - Immunochemical staining of human GADD153/CHOP in human pancreas with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/GADD153-CHOP-Antibody-Immunohistochemistry-Paraffin-NBP2-98742-img0002.jpg "Immunohistochemistry-Paraffin: GADD153/CHOP Antibody [NBP2-98742] - Immunochemical staining of human GADD153/CHOP in human pancreas with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).")
![Immunocytochemistry/Immunofluorescence: GADD153/CHOP Antibody [NBP2-98742] - Immunofluorescence staining of GADD153/CHOP in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98742 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green).Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-98742_rabbit-polyclonal-gadd153-chop-antibody-235202521525024.png)
![Western Blot: AIF-1/Iba1 Antibody (2A2-B6) [H00000199-M01] - Analysis of AIF1 expression in K-562 using AIF-1/Iba1 Antibody (2A2-B6).](http://images.novusbio.com/fullsize/AIF-1-Iba1-Antibody-2A2-B6-Western-Blot-H00000199-M01-img0005.jpg "Western Blot: AIF-1/Iba1 Antibody (2A2-B6) [H00000199-M01] - Analysis of AIF1 expression in K-562 using AIF-1/Iba1 Antibody (2A2-B6).")
![ELISA: AIF-1/Iba1 Antibody (2A2-B6) [H00000199-M01] - Detection limit for recombinant GST tagged AIF-1:Iba1 is 0.03 ng/ml using AIF-1:Iba1 Antibody (2A2-B6) as a capture antibody.](http://images.novusbio.com/fullsize/AIF-1-Iba1-Antibody-2A2-B6-ELISA-H00000199-M01-img0004.jpg)
![ELISA: BTLA/CD272 Antibody (HMBT-6B2) - Chimeric [NBP2-81118] - ELISA of anti-BTLA antibody on BTLA-Fc fusion protein. Binding curves of the rabbit IgG chimeric version of the (NBP2-81118; red line) and isotype control (NBP2-52638, anti-Fluorescein; blue line) to an ELISA plate coated with BTLA-Fc fusion protein at a concentration of 5 ug/ml. A 3-fold serial dilution from 10,000 to 0.17 ng/ml of NBP2-81118 was used. For signal detection, a 1:4000 dilution of anti-rabbit IgG1 antibody was used. The second increase in absorbance at 3333ng/ml is suggestive of a possible secondary binding epitope for NBP2-81118 on BTLA-Fc fusion protein.](http://images.novusbio.com/fullsize/BTLA-CD272-Antibody-HMBT-6B2-Chimeric-ELISA-NBP2-81118-img0001.jpg "ELISA: BTLA/CD272 Antibody (HMBT-6B2) - Chimeric [NBP2-81118] - ELISA of anti-BTLA antibody on BTLA-Fc fusion protein. Binding curves of the rabbit IgG chimeric version of the (NBP2-81118; red line) and isotype control (NBP2-52638, anti-Fluorescein; blue line) to an ELISA plate coated with BTLA-Fc fusion protein at a concentration of 5 ug/ml. A 3-fold serial dilution from 10,000 to 0.17 ng/ml of NBP2-81118 was used. For signal detection, a 1:4000 dilution of anti-rabbit IgG1 antibody was used. The second increase in absorbance at 3333ng/ml is suggestive of a possible secondary binding epitope for NBP2-81118 on BTLA-Fc fusion protein.")