| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-87270-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21180-25ul | |||
| Azide and BSA Free | NBP3-44262 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-97476-0.2mg | |||
| BSA Free | NBP1-97476-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-74048SS | |||
![Western Blot: MEF2A Antibody (1C8) [H00004205-M15] - Analysis of MEF2A expression in MCF-7 (Cat # L046V1).](http://images.novusbio.com/fullsize/MEF2A-Antibody-1C8-Western-Blot-H00004205-M15-img0008.jpg "Western Blot: MEF2A Antibody (1C8) [H00004205-M15] - Analysis of MEF2A expression in MCF-7 (Cat # L046V1).")
![Immunocytochemistry/Immunofluorescence: MEF2A Antibody (1C8) [H00004205-M15] - Analysis of monoclonal antibody to MEF2A on MCF-7 cell. Image from verified customer review](http://images.novusbio.com/fullsize/MEF2A-Antibody-1C8-Immunocytochemistry-Immunofluorescence-H00004205-M15-img0009.jpg)
![Western Blot: MEF2A Antibody (1C8) [H00004205-M15] - Analysis of MEF2A expression in HepG2 (Cat # L019V1).](http://images.novusbio.com/fullsize/MEF2A-Antibody-1C8-Western-Blot-H00004205-M15-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: MEF2A Antibody (1C8) [H00004205-M15] - Analysis of monoclonal antibody to MEF2A on MCF-7 cell. Antibody concentration 10 ug/ml](http://images.novusbio.com/fullsize/MEF2A-Antibody-1C8-Immunocytochemistry-Immunofluorescence-H00004205-M15-img0006.jpg)
![ELISA: MEF2A Antibody (1C8) [H00004205-M15] - Detection limit for recombinant GST tagged MEF2A is approximately 0.3ng/ml as a capture antibody.](http://images.novusbio.com/fullsize/MEF2A-Antibody-1C8-ELISA-H00004205-M15-img0004.jpg)
![Western Blot: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Analysis of NMDAR1 on different cells lysates using anti-NMDAR1 antibody at 1/500 dilution. Positive control: Line 1: MCF-7 Line 2: A549](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Western-Blot-NBP2-66982-img0004.jpg "Western Blot: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Analysis of NMDAR1 on different cells lysates using anti-NMDAR1 antibody at 1/500 dilution. Positive control: Line 1: MCF-7 Line 2: A549")
![Immunocytochemistry/Immunofluorescence: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Staining NMDAR1 in SH-SY5Y cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Immunocytochemistry-Immunofluorescence-NBP2-66982-img0005.jpg)
![Immunohistochemistry-Paraffin: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Analysis of paraffin-embedded rat brain tissue using anti-NMDAR1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Immunohistochemistry-Paraffin-NBP2-66982-img0003.jpg)
![Flow Cytometry: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Analysis of SH-SY5Y cells with NMDAR1 antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Flow-Cytometry-NBP2-66982-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Staining NMDAR1 in SHG-44 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Immunocytochemistry-Immunofluorescence-NBP2-66982-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Staining NMDAR1 in N2A cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Immunocytochemistry-Immunofluorescence-NBP2-66982-img0006.jpg)
![Immunohistochemistry-Paraffin: NMDAR1 Antibody (JM11-26) [NBP2-66982] - Analysis of paraffin-embedded mouse brain tissue using anti-NMDAR1 antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/NMDAR1-Antibody-JM11-26-Immunohistochemistry-Paraffin-NBP2-66982-img0002.jpg)
![Immunohistochemistry-Paraffin: Chk1 [p Ser296] Antibody (SN06-50) [NBP2-67711] - Analysis of paraffin-embedded human tonsil tissue using anti- phospho-Chk1 (S296) antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Chk1-p-Ser296-Antibody-SN06-50-Immunohistochemistry-Paraffin-NBP2-67711-img0002.jpg "Immunohistochemistry-Paraffin: Chk1 [p Ser296] Antibody (SN06-50) [NBP2-67711] - Analysis of paraffin-embedded human tonsil tissue using anti- phospho-Chk1 (S296) antibody. Counter stained with hematoxylin.")
![Immunohistochemistry-Paraffin: Chk1 [p Ser296] Antibody (SN06-50) [NBP2-67711] - Analysis of paraffin-embedded human breast carcinoma tissue using anti- phospho-Chk1 (S296) antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/Chk1-p-Ser296-Antibody-SN06-50-Immunohistochemistry-Paraffin-NBP2-67711-img0001.jpg)
![Western Blot: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Analysis of Phospho-PKR(T446) on different lysates using anti-Phospho-PKR(T446) antibody at 1/1,000 dilution. Positive control: Lane 1: Hela treated with Calyculin A and TNF-alpha whole cell lysates Lane 2: Untreated Hela whole cell lysates](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Western-Blot-NBP2-67426-img0002.jpg "Western Blot: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Analysis of Phospho-PKR(T446) on different lysates using anti-Phospho-PKR(T446) antibody at 1/1,000 dilution. Positive control: Lane 1: Hela treated with Calyculin A and TNF-alpha whole cell lysates Lane 2: Untreated Hela whole cell lysates")
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-PKR antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-20, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0008.jpg)
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Analysis of paraffin-embedded human kidney tissue using anti-Phospho-PKR(T446) antibody. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0001.jpg)
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-PKR antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-20, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0003.jpg)
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Immunohistochemical analysis of paraffin-embedded human breast tissue using anti-PKR antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-20, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0004.jpg)
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-PKR antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-20, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0005.jpg)
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Immunohistochemical analysis of paraffin-embedded human small intestine tissue using anti-PKR antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-20, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0006.jpg)
![Immunohistochemistry-Paraffin: PKR [p Thr446] Antibody (SY230) [NBP2-67426] - Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-PKR antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1607-20, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/PKR-p-Thr446-Antibody-SY230-Immunohistochemistry-Paraffin-NBP2-67426-img0007.jpg)
![Western Blot: Nrf2 [p Ser40] Antibody (SU0334) [NBP2-67465] - Western blot analysis of Nrf2 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabb](http://images.novusbio.com/fullsize/Nrf2-p-Ser40-Antibody-SU0334-Western-Blot-NBP2-67465-img0009.jpg "Western Blot: Nrf2 [p Ser40] Antibody (SU0334) [NBP2-67465] - Western blot analysis of Nrf2 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabb")
![Flow Cytometry: Nrf2 [p Ser40] Antibody (SU0334) [NBP2-67465] -Analysis of RIP3 was done on SW620 cells. The cells were fixed, permeabilized and stained with the primary antibody (1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp2-67465_rabbit-monoclonal-nrf2-p-ser40-antibody-su0334-flow-cytometry-2572024102417..jpg)
![Immunohistochemistry-Paraffin: Nrf2 [p Ser40] Antibody (SU0334) [NBP2-67465] -Rat kidney tissue using anti-RIP3 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.](http://images.novusbio.com/fullsize/nbp2-67465_rabbit-monoclonal-nrf2-p-ser40-antibody-su0334-immunohistochemistry-paraffin-2572024102613..jpg)
![Western Blot: Nrf2 [p Ser40] Antibody (SU0334) [NBP2-67465] - Analysis of RIP3 on HT-29 cell lysates with Rabbit anti-RIP3 antibody at 1/1,000 dilution.Lysates/proteins at 10 ug/Lane.Predicted band size: 57 kDaObserved band size: 50 kDaExposure time: 2 minutes;12% SDS-PAGE gel.Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp2-67465_rabbit-monoclonal-nrf2-p-ser40-antibody-su0334-western-blot-2572024102740..jpg)
![Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Analysis in human cerebral cortex and skeletal muscle tissues. Corresponding PRKCZ RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunohistochemistry-Paraffin-NBP1-87270-img0016.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Analysis in human cerebral cortex and skeletal muscle tissues. Corresponding PRKCZ RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Western Blot: PKC zeta Antibody [NBP1-87270] - Lane 1: Marker [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11. Lane 2: Human cell line RT-431](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Western-Blot-NBP1-87270-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: PKC zeta Antibody [NBP1-87270] - Staining of human cell line U-251 MG shows localization to plasma membrane and cytosol. Antibody staining is shown in green.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-87270-img0015.jpg)
![Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Staining of human skeletal muscle shows no positivity in myocytes as expected.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunohistochemistry-Paraffin-NBP1-87270-img0020.jpg)
![Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Staining of human retina shows strong cytoplasmic and membranous positivity in photoreceptor cells.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunohistochemistry-Paraffin-NBP1-87270-img0012.jpg)
![Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Staining of human cerebral cortex shows moderate positivity in neuropil.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunohistochemistry-Paraffin-NBP1-87270-img0017.jpg)
![Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Staining of human duodenum shows moderate cytoplasmic/ membranous positivity in glandular cells.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunohistochemistry-Paraffin-NBP1-87270-img0018.jpg)
![Immunohistochemistry-Paraffin: PKC zeta Antibody [NBP1-87270] - Staining of human placenta shows weak cytoplasmic positivity in trophoblastic cells.](http://images.novusbio.com/fullsize/PKC-zeta-Antibody-Immunohistochemistry-Paraffin-NBP1-87270-img0019.jpg)
![Immunohistochemistry-Paraffin: RelB Antibody [NBP2-20123] - Human breast carcinoma. RelB stained by RelB antibody diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.](http://images.novusbio.com/fullsize/RelB-Antibody-Immunohistochemistry-Paraffin-NBP2-20123-img0014.jpg "Immunohistochemistry-Paraffin: RelB Antibody [NBP2-20123] - Human breast carcinoma. RelB stained by RelB antibody diluted at 1:500.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min.")
![<b>Biological Strategies Validation. </b>Chromatin Immunoprecipitation: RelB Antibody [NBP2-20123] - Cross-linked ChIP was performed with THP-1 chromatin extract treated with LPS (1.0 ug/ml for 3 h) and 5 ug of either normal rabbit IgG or anti-RelB antibody. The precipitated DNA was detected by PCR with primer set targeting to IL-1 beta promoter.](http://images.novusbio.com/fullsize/RelB-Antibody-Chromatin-Immunoprecipitation-ChIP-NBP2-20123-img0009.jpg)
![Western Blot: Rel B Antibody [NBP2-20123] - Sample (30 ug of whole cell lysate) A: NIH-3T3 7. 5% SDS PAGE gel, diluted at 1:10000.](http://images.novusbio.com/fullsize/Rel-B-Antibody-Western-Blot-NBP2-20123-img0002.jpg)
![Western Blot: RelB Antibody [NBP2-20123] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with RelB antibody 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/RelB-Antibody-Western-Blot-NBP2-20123-img0011.jpg)
![Immunoprecipitation: RelB Antibody [NBP2-20123] - HeLa whole cell lysate/extract A. Control with 2 ug of preimmune rabbit IgG B. Immunoprecipitation of RelB protein by 2 ug of RelB antibody 7.5% SDS-PAGE The immunoprecipitated RelB protein was detected by RelB antibody ) diluted at 1:1000. EasyBlot anti-rabbit IgG was used as a secondary reagent.](http://images.novusbio.com/fullsize/RelB-Antibody-Immunoprecipitation-NBP2-20123-img0006.jpg)
![Western Blot: Rabbit Polyclonal RelB Antibody [NBP2-20123] - Whole cell lysates from MDA-MB-231, SUM159, MCF-7 and HEK293T cells were loaded with 50 ug/lane. 10% SDS-PAGE. RRS1 Antibody (NBP2-49323) was used for primary antibody: 1:1000, 4C, overnight. Image from a verified customer review.](http://images.novusbio.com/fullsize/antibody/nbp2-20123_rabbit-polyclonal-relb-antibody-western-blot-311202415821..jpg)
![Western Blot: RelB Antibody [NBP2-20123] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with RelB antibody (NBP2-20123) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-20123_rabbit-polyclonal-relb-antibody-91020242075935.jpg)
![Western Blot: Histone H4 Antibody [NBP2-42856] - Various tissue extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with Histone H4 antibody diluted at 1:1000.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Western-Blot-NBP2-42856-img0008.jpg "Western Blot: Histone H4 Antibody [NBP2-42856] - Various tissue extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with Histone H4 antibody diluted at 1:1000.")
![Immunocytochemistry/Immunofluorescence: Histone H4 Antibody [NBP2-42856] - Analysis of Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: Histone H4 protein stained by Histone H4 antibody diluted at 1:5000. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [114] diluted at 1:2000. Blue: Hoechst 33342 staining.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-42856-img0006.jpg)
![Immunohistochemistry-Paraffin: Histone H4 Antibody [NBP2-42856] - Rat brain stem. Histone H4 antibody dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Immunohistochemistry-Paraffin-NBP2-42856-img0004.jpg)
![Western Blot: Histone H4 Antibody [NBP2-42856] - Analysis of various whole cell extracts (30 ug) were separated by 15% SDS-PAGE, and the membrane was blotted with Histone H4 antibody diluted at a dilution of 1:5000.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Western-Blot-NBP2-42856-img0005.jpg)
![Immunohistochemistry-Paraffin: Histone H4 Antibody [NBP2-42856] - Mouse fore brain. Histone H4 antibody dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Immunohistochemistry-Paraffin-NBP2-42856-img0001.jpg)
![Immunohistochemistry-Paraffin: Histone H4 Antibody [NBP2-42856] - Mouse fore brain. Histone H4 antibody dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Immunohistochemistry-Paraffin-NBP2-42856-img0002.jpg)
![Immunohistochemistry-Paraffin: Histone H4 Antibody [NBP2-42856] - Mouse muscle. Histone H4 antibody dilution: 1:500. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min.](http://images.novusbio.com/fullsize/Histone-H4-Antibody-Immunohistochemistry-Paraffin-NBP2-42856-img0003.jpg)
![Western Blot: Calnexin Antibody [NBP1-97476] - Lane 1: MWM, Lane 2: Vero, Lane 3: 3T3, Lane 4: PC-12, Lane 5: HeLa.](http://images.novusbio.com/fullsize/Calnexin-Antibody-Western-Blot-NBP1-97476-img0002.jpg "Western Blot: Calnexin Antibody [NBP1-97476] - Lane 1: MWM, Lane 2: Vero, Lane 3: 3T3, Lane 4: PC-12, Lane 5: HeLa.")
![Immunohistochemistry-Paraffin: Calnexin Antibody [NBP1-97476] - Analysis of human placenta tissue stained with Calnexin, pAb at 5ug/ml.](http://images.novusbio.com/fullsize/Calnexin-Antibody-Immunohistochemistry-Paraffin-NBP1-97476-img0001.jpg)
![Western Blot: RelA/NFkB p65 [p Ser529] Antibody [NBP1-77808] - TNF Induces phosphorylation of p65 in KBM-5 cells. Nuclear protein lysates prepared after 0, 5, 10, 15, 30 and 60 minutes of 0.1 nM TNF treatment of KBM-5 cells shows inducible phosphorylation using phospho specific polyclonal anti-human pS529 p65. Anti-beta-actin staining confirms loading of equivalent amounts of protein. HRP conjugated Gt-anti-Rabbit IgG used to develop blot using a chemiluminescent detection method. Other detection methods will yield similar results.](http://images.novusbio.com/fullsize/RelA-NFkB p65 [p Ser529] Antibody-Western Blot-NBP1-77808-img0005.jpg "Western Blot: RelA/NFkB p65 [p Ser529] Antibody [NBP1-77808] - TNF Induces phosphorylation of p65 in KBM-5 cells. Nuclear protein lysates prepared after 0, 5, 10, 15, 30 and 60 minutes of 0.1 nM TNF treatment of KBM-5 cells shows inducible phosphorylation using phospho specific polyclonal anti-human pS529 p65. Anti-beta-actin staining confirms loading of equivalent amounts of protein. HRP conjugated Gt-anti-Rabbit IgG used to develop blot using a chemiluminescent detection method. Other detection methods will yield similar results.")
![Western Blot: RelA/NFkB p65 [p Ser529] Antibody [NBP1-77808] - pS529 shows phospho p65 staining in carcinoma cells. western blot of total protein lysates from various human head and neck tumors shows phospho p65 staining in tumor cell lines using phospho specific polyclonal anti-human pS529 p65. Lanes 1-6 contain protein lysates from human squamal carcinoma cell lines. Lane 7 is a protein lysate from a primary culture of human keratinocytes. Lane 8 contains protein lysate from ATCC SCC9 cells (also a head and neck squamal carcinoma). Lane 9 contains lysate from EGF-induced human derived A431 cells. Lane 10 (not shown) contains a molecular weight standard. Concurrent staining with anti-beta microtubulin (not shown) was used to confirm equal protein loading in all lanes. HRP conjugated Gt-anti-Rabbit IgG was used to develop the blot using a chemiluminescent detection method.](http://images.novusbio.com/fullsize/RelA-NFkB-p65-[p-Ser529]-Antibody-Western-Blot-NBP1-77808-img0003.jpg)
![Western Blot: RelA/NFkB p65 [p Ser529] Antibody [NBP1-77808] - TNF Induces phosphorylation of p65 in KBM-5 cells. Cytoplasmic and nuclear protein lysates prepared after 0, 5, 10, 15, 30 and 60 minutes of 0.1 nM TNF treatment of KBM-5 cells shows inducible phosphorylation using phospho specific polyclonal anti-human pS276 p65. Pan reactive anti p65 (NBP1-77808) was used a control to show the presence of total p65 in both the cytoplasmic and nuclear extracts. Phosphorylation of p65 occurs after approximately 10 min of TNF exposure. Migration of phosphorylated p65 into the nucleus occurs within a similar time frame. HRP conjugated Gt-anti-Rabbit IgG was used to develop the western blot using a chemi-luminescent detection method.](http://images.novusbio.com/fullsize/RelA-NFkB-p65-[p-Ser529]-Antibody-Western-Blot-NBP1-77808-img0004.jpg)
![Western Blot: LSP1 Antibody [NBP1-74048] - Western blot analysis of LSP1 in Ramos (1) and Daudi (2) cell lysates.](http://images.novusbio.com/fullsize/LSP1-Antibody-Western-Blot-NBP1-74048-img0003.jpg "Western Blot: LSP1 Antibody [NBP1-74048] - Western blot analysis of LSP1 in Ramos (1) and Daudi (2) cell lysates.")
![Immunohistochemistry-Paraffin: LSP1 Antibody [NBP1-74048] - IHC analysis of LSP1 in mouse colon tissue. Abundant membrane staining is visible in the epithelial cells.](http://images.novusbio.com/fullsize/LSP1-Antibody-Immunohistochemistry-Paraffin-NBP1-74048-img0002.jpg)