| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | MAB3664-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-56888SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | MAB6000-SP | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-56170SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-33220 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-56172SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB110-41572SS | |||
| Azide and BSA Free | NBP2-80672 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-04965-0.025ml | |||
![Western Blot: Apolipoprotein A-I/ApoA1 Antibody (2083D) [MAB3664] - Analysis of HepG2 cell lysate with 0.1 ug/ml of hApoA1 Monoclonal Antibody followed by HRP-conjugated Anti-Rabbit IgG Antibody. A specific band was detected for hApoA1 at approximately 25-30 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.](http://images.novusbio.com/fullsize/Apolipoprotein-A-I-ApoA1-Antibody-2083D-Western-Blot-MAB3664-img0002.jpg "Western Blot: Apolipoprotein A-I/ApoA1 Antibody (2083D) [MAB3664] - Analysis of HepG2 cell lysate with 0.1 ug/ml of hApoA1 Monoclonal Antibody followed by HRP-conjugated Anti-Rabbit IgG Antibody. A specific band was detected for hApoA1 at approximately 25-30 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.")
![Immunocytochemistry: Apolipoprotein A-I/ApoA1 Antibody (2083D) [MAB3664] - ApoA1 was detected in immersion fixed HepG2 cell using ApoA1 Monoclonal Antibody at 1 ug/ml dilution. Cells were stained using the NorthernLights 557-conjugated Anti-Rabbit IgG Secondary Antibody (red) and counterstained with DAPI (blue). Specific staining was localized to cytoplasmic.](http://images.novusbio.com/fullsize/Apolipoprotein-A-I-ApoA1-Antibody-2083D-Immunocytochemistry-MAB3664-img0001.jpg)
![Immunohistochemistry: Apolipoprotein A-I/ApoA1 Antibody (2083D) [MAB3664] - ApoA1 was detected in immersion fixed paraffin-embedded sections of human lung cancer using ApoA1 Monoclonal Antibody at 1 ug/ml. Tissue was stained using Rabbit IgG VisUCyte HRP Polymer Antibody (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm in cancer cells.](http://images.novusbio.com/fullsize/Apolipoprotein-A-I-ApoA1-Antibody-2083D-Immunohistochemistry-MAB3664-img0003.jpg)
![Flow Cytometry: Apolipoprotein A-I/ApoA1 Antibody (2083D) [MAB3664] - An intracellular stain was performed on HepG2 cells with Apolipoprotein A-I/ApoA1 Antibody (2083D) MAB3664AF488 (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 10 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 488.](http://images.novusbio.com/fullsize/Apolipoprotein-A-I-ApoA1-Antibody-2083D-Flow-Cytometry-MAB3664-img0006.jpg)
![Flow Cytometry: Apolipoprotein A-I/ApoA1 Antibody (2083D) [MAB3664] - HepG2 human hepatocellular carcinoma cell line was stained with Rabbit Anti-Human Apolipoprotein A-I/ApoA1 Monoclonal Antibody (Catalog # MAB3664, filled histogram) or isotype control antibody (Catalog # AB-105-C, open histogram), followed by Phycoerythrin-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # F0102B). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005).](http://images.novusbio.com/fullsize/Apolipoprotein-A-I-ApoA1-Antibody-2083D-Flow-Cytometry-MAB3664-img0005.jpg)
![Western Blot: RB1 Antibody [NB100-56888] - Analysis of Retinoblastoma 1 in 30 ugs of Jurkat cell lysate using NB100-56888 at 1:1000 dilution.](http://images.novusbio.com/fullsize/RB1-Antibody-Western-Blot-NB100-56888-img0003.jpg "Western Blot: RB1 Antibody [NB100-56888] - Analysis of Retinoblastoma 1 in 30 ugs of Jurkat cell lysate using NB100-56888 at 1:1000 dilution.")
![Western Blot: Cyclin B1 Antibody (2061A) - Azide Free [MAB6000] - Western blot detection of Cyclin B1 (clone 2061A) catalog number MAB6000 at 0.05 ug/ml in HeLa and Jurkat cell lysates.](http://images.novusbio.com/fullsize/Cyclin-B1-Antibody-2061A-Azide-Free-Western-Blot-MAB6000-img0002.jpg "Western Blot: Cyclin B1 Antibody (2061A) - Azide Free [MAB6000] - Western blot detection of Cyclin B1 (clone 2061A) catalog number MAB6000 at 0.05 ug/ml in HeLa and Jurkat cell lysates.")
![Immunohistochemistry: Cyclin B1 Antibody (2061A) - Azide Free [MAB6000] - Cyclin B1 was detected in immersion fixed paraffin-embedded sections of human squamous cell carcinoma using Cyclin B1 Monoclonal Antibody at 3 ug/ml. Tissue was stained using Rabbit IgG VisUCyte HRP Polymer Antibody (brown) and counterstained with hematoxylin (blue). Specific staining was localized to nuclei in cancer cells.](http://images.novusbio.com/fullsize/Cyclin-B1-Antibody-2061A-Azide-Free-Immunohistochemistry-MAB6000-img0003.jpg)
![Flow Cytometry: Cyclin B1 Antibody (2061A) - Azide Free [MAB6000] - An intracellular stain was performed on HeLa cells with Cyclin B1 Antibody [2061A] MAB6000F (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 10 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to FITC.](http://images.novusbio.com/fullsize/Cyclin-B1-Antibody-2061A-Azide-Free-Flow-Cytometry-MAB6000-img0004.jpg)
![Flow Cytometry: Cyclin B1 Antibody (2061A) - Azide Free [MAB6000] - K562 human cell line was stained with Rabbit Anti-Human Cyclin B1 Monoclonal Antibody (Catalog # MAB6000, filled histogram) or isotype control antibody (open histogram), followed by Phycoerythrin-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog # F0110). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005).](http://images.novusbio.com/fullsize/Cyclin-B1-Antibody-2061A-Azide-Free-Flow-Cytometry-MAB6000-img0001.jpg)
![Western Blot: TRAF-1 Antibody [NB100-56170] - Analysis of TRAF-1 in normal human tissues using this antibody. TRAF-1 is observed at 50-50 kDa. Additional bands of lower molecular weight were seen in some cases, and may represent TRAF-1 degradation fragments.](http://images.novusbio.com/fullsize/TRAF-1-Antibody-Western-Blot-NB100-56170-img0009.jpg "Western Blot: TRAF-1 Antibody [NB100-56170] - Analysis of TRAF-1 in normal human tissues using this antibody. TRAF-1 is observed at 50-50 kDa. Additional bands of lower molecular weight were seen in some cases, and may represent TRAF-1 degradation fragments.")
![Immunohistochemistry-Paraffin: TRAF-1 Antibody [NB100-56170] - Formalin-fixed, paraffin-embedded human tissue sections stained for TRAF-1 expression using NB100-56170 at 1:2000. Hematoxylin-eosin counterstain. A, A1: Formalin-fixed, paraffin-embedded human lymphoma tissue section stained for TRAF-1 expression using NB100-56170 at 1:2000. Hematoxylin-eosin counterstain. A, Hodgkin'sDisease, the Reed-Sternberg cells are positive for TRAF-1 expression. B, lymph node, dendritic-like cells are positive for TRAF-1 expression. A1 and B1 are higher magnifications from A and B, respectively.](http://images.novusbio.com/fullsize/TRAF-1-Antibody-Immunohistochemistry-Paraffin-NB100-56170-img0008.jpg)
![Immunohistochemistry-Paraffin: TRAF-1 Antibody [NB100-56170] - Formalin-fixed, paraffin-embedded human lymphoma tissue section stained for TRAF-1 expression using NB100-56170 at 1:2000. Hematoxylin-eosin counterstain. A1 is a higher magnification of A.](http://images.novusbio.com/fullsize/TRAF-1-Antibody-Immunohistochemistry-Paraffin-NB100-56170-img0006.jpg)
![Western Blot: hHpr1-p84-Thoc1 Antibody [NBP2-16822] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with hHpr-p84-Thoc1 Antibody diluted at 1:2000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/hHpr1-p84-Thoc1-Antibody-Western-Blot-NBP2-16822-img0011.jpg "Western Blot: hHpr1-p84-Thoc1 Antibody [NBP2-16822] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with hHpr-p84-Thoc1 Antibody diluted at 1:2000. HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.")
![Immunohistochemistry-Paraffin: hHpr1-p84-Thoc1 Antibody [NBP2-16822] - Immunohistochemical analysis of paraffin-embedded NCIN87 xenograft, using antibody at 1:500 dilution.](http://images.novusbio.com/fullsize/hHpr1-p84-Thoc1-Antibody-Immunohistochemistry-Paraffin-NBP2-16822-img0002.jpg)
![Western Blot: hHpr1-p84-Thoc1 Antibody [NBP2-16822] - Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Nuclear Matrix Protein p84 antibody [C1C3] 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/hHpr1-p84-Thoc1-Antibody-Western-Blot-NBP2-16822-img0004.jpg)
![Immunoprecipitation: hHpr1-p84-Thoc1 Antibody [NBP2-16822] - HepG2 whole cell lysate/extract A : 30 ug whole cell lysate/extract of p84 protein expressing HepG2 cells B : Control with 3 ug of pre-immune rabbit IgG C : Immunoprecipitation of p84 by 3 ug of Nuclear Matrix Protein p84 antibody [C1C3] 7.5% SDS-PAGE The immunoprecipitated p84 protein was detected by Nuclear Matrix Protein p84 antibody [C1C3] diluted at 1 : 1000. EasyBlot anti-rabbit IgG (HRP) was used as a secondary reagent.](http://images.novusbio.com/fullsize/hHpr1-p84-Thoc1-Antibody-Immunoprecipitation-NBP2-16822-img0006.jpg)
![Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Nuclear Matrix Protein p84 antibody [C1C3] (NBP2-16822) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-16822_rabbit-polyclonal-hhpr1-p84-thoc1-antibody-western-blot-2611202518274610.jpg)
![Nuclear Matrix Protein p84 antibody [C1C3] detects Nuclear Matrix Protein p84 protein at cytoplasm and nucleus by immunofluorescent analysis.Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: Nuclear Matrix Protein p84 protein stained by Nuclear Matrix Protein p84 antibody [C1C3] (NBP2-16822) diluted at 1:500.Blue: Hoechst 33342 staining.](http://images.novusbio.com/fullsize/nbp2-16822_rabbit-polyclonal-hhpr1-p84-thoc1-antibody-immunocytochemistry-immunofluorescence-261120251848236.jpg)
![Western Blot: IKK gamma Antibody (46B844) [NB100-56532] - Analysis using NEMO (IKKgamma) antibody. Lysate from human Jurkat cells probed with NEMO antibody at 2 ug/ml. The goat anti-mouse IgG1 HRP secondary and PicoTect ECL substrate solution were used for this test.](http://images.novusbio.com/fullsize/IKK-gamma-Antibody-46B844-Western-Blot-NB100-56532-img0007.jpg "Western Blot: IKK gamma Antibody (46B844) [NB100-56532] - Analysis using NEMO (IKKgamma) antibody. Lysate from human Jurkat cells probed with NEMO antibody at 2 ug/ml. The goat anti-mouse IgG1 HRP secondary and PicoTect ECL substrate solution were used for this test.")
![Flow Cytometry: IKK gamma Antibody (46B844) [NB100-56532] - Human Jurkat cells were probed using 0.1 ug of NEMO antibody (red) and 0.1 ug of isotype control (green), with shaded histogram representing cells alone and an anti-mouse IgG-FITC secondary antibody.](http://images.novusbio.com/fullsize/IKK-gamma-Antibody-46B844-Flow-Cytometry-NB100-56532-img0005.jpg)
![Immunohistochemistry-Paraffin: TRAF-2 Antibody [NB100-56172] - Analysis of TRAF-2 in formalin-fixed, paraffin-embedded normal human thymus sections using NB100-56172 at 1:2000. A-C, successively higher magnifications. Hematoxylin-eosin counterstain.](http://images.novusbio.com/fullsize/TRAF-2-Antibody-Immunohistochemistry-Paraffin-NB100-56172-img0006.jpg "Immunohistochemistry-Paraffin: TRAF-2 Antibody [NB100-56172] - Analysis of TRAF-2 in formalin-fixed, paraffin-embedded normal human thymus sections using NB100-56172 at 1:2000. A-C, successively higher magnifications. Hematoxylin-eosin counterstain.")
![Immunohistochemistry: TRAF-2 Antibody [NB100-56172] - Analysis of TRAF2 in formalin-fixed, paraffin-embedded normal human bone marrow section using NB100-56172 at 1:2000. Hematoxylin-eosin counterstain.](http://images.novusbio.com/fullsize/TRAF-2-Antibody-Immunohistochemistry-NB100-56172-img0005.jpg)
![Western Blot: SRC1 Antibody (1135/H4) [NB200-310] - Mouse tissue (50 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with SRC1 antibody [1135] diluted at 1:2000.](http://images.novusbio.com/fullsize/SRC1-Antibody-1135-H4-Western-Blot-NB200-310-img0003.jpg "Western Blot: SRC1 Antibody (1135/H4) [NB200-310] - Mouse tissue (50 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with SRC1 antibody [1135] diluted at 1:2000.")
![Western Blot: CITED4 Antibody (HT13-2D6.3) [NB110-41572] - Detection of human CITED4 in 20ug of transfected whole cell Hep3B lysate using NB110-415752. Photo courtesy of Dr. DeCaprio, DFCI.](http://images.novusbio.com/fullsize/CITED4-Antibody-HT13-2D6-3-Western-Blot-NB110-41572-img0003.jpg "Western Blot: CITED4 Antibody (HT13-2D6.3) [NB110-41572] - Detection of human CITED4 in 20ug of transfected whole cell Hep3B lysate using NB110-415752. Photo courtesy of Dr. DeCaprio, DFCI.")
![Immunohistochemistry-Paraffin: CITED4 Antibody (HT13-2D6.3) [NB110-41572] - CITED4 was detected in immersion fixed paraffin-embedded sections of human heart using Mouse Anti-Human CITED4 (HT13-2D6.3) Monoclonal Antibody (Catalog # NB110-41572) at 1:300 for 1 hour at room temperature followed by incubation with the Anti-Mouse IgG VisUCyte™ HRP Polymer Antibody (Catalog # VC001). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to the cytoplasm in cardiomyocytes.](http://images.novusbio.com/fullsize/CITED4-Antibody-HT13-2D6-3-Immunohistochemistry-Paraffin-NB110-41572-img0009.jpg)
![Flow Cytometry: CITED4 Antibody (HT13-2D6.3) [NB110-41572] - Intracellular flow cytometric staining of 1 x 10^6 CHO (A) and HEK-293 (B) cells using CITED4 antibody (dark blue). Isotype control shown in orange. An antibody concentration of 1 ug/1x10^6 cells was used.](http://images.novusbio.com/fullsize/CITED4-Antibody-HT13-2D6-3-Flow-Cytometry-NB110-41572-img0008.jpg)
![Immunohistochemistry: Alpha Dystroglycan Antibody (2238) [NBP1-49634] - Endothelial B-catenin GOF does not affect astrocytic endfoot polarization of a-dystroglycan (a-Dag) and Kir4.1 within the subfornical organ (SFO). Striatal BBB-vessel showing a polarized distribution of a-Dag and Kir4.1 in AC endfeet. Lumen is stained by Podxl (asterisk) (A). Coronal overview of the subfornical organ (SFO) (B); rectangular inset demarcates area for higher magnification in (C). Dashed lines outline SFO vessels. Scale bar show 2 um (A), 50 um (B), 10 um (C). Image collected and cropped by CiteAb from the following publication (elifesciences.org/articles/43818), licensed under a CC-BY license.](http://images.novusbio.com/fullsize/Alpha-Dystroglycan-Antibody-2238-Immunohistochemistry-NBP1-49634-img0002.jpg "Immunohistochemistry: Alpha Dystroglycan Antibody (2238) [NBP1-49634] - Endothelial B-catenin GOF does not affect astrocytic endfoot polarization of a-dystroglycan (a-Dag) and Kir4.1 within the subfornical organ (SFO). Striatal BBB-vessel showing a polarized distribution of a-Dag and Kir4.1 in AC endfeet. Lumen is stained by Podxl (asterisk) (A). Coronal overview of the subfornical organ (SFO) (B); rectangular inset demarcates area for higher magnification in (C). Dashed lines outline SFO vessels. Scale bar show 2 um (A), 50 um (B), 10 um (C). Image collected and cropped by CiteAb from the following publication (elifesciences.org/articles/43818), licensed under a CC-BY license.")
![Immunocytochemistry/ Immunofluorescence: Alpha Dystroglycan Antibody (2238) [NBP1-49634] - Endothelial beta -catenin GOF does not affect astrocytic endfoot polarization of alpha -dystroglycan ( alpha -Dag) & Kir4.1 within the subfornical organ (SFO).Striatal BBB-vessel showing a polarized distribution of alpha -Dag & Kir4.1 in AC endfeet. Lumen is stained by Podxl (asterisk) (A). Coronal overview of the subfornical organ (SFO) (B); rectangular inset demarcates area for higher magnification in (C). Dashed lines outline SFO vessels. Scale bar show 2 µm (A), 50 µm (B), 10 µm (C). Image collected & cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/30932814), licensed under a CC-BY license. Not internally tested by Novus Biologicals.](http://images.novusbio.com/fullsize/nbp1-49634_mouse-monoclonal-alpha-dystroglycan-antibody-2238-31020241535688.jpg)
![Western Blot: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Western blot analysis of VEGFR1/Flt-1 on mouse lung lysates using NBP3-11864 at 1/1,000 dilution.](http://images.novusbio.com/fullsize/VEGFR1-Flt-1-Antibody-SY09-09-Western-Blot-NBP3-11864-img0001.jpg "Western Blot: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Western blot analysis of VEGFR1/Flt-1 on mouse lung lysates using NBP3-11864 at 1/1,000 dilution.")
![Immunocytochemistry/Immunofluorescence: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - ICC staining VEGFR1/Flt-1 in SHG-44 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/VEGFR1-Flt-1-Antibody-SY09-09-Immunocytochemistry-Immunofluorescence-NBP3-11864-img0006.jpg)
![Immunohistochemistry-Paraffin: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Immunohistochemical analysis of paraffin-embedded mouse brain tissue using NBP3-11864. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/VEGFR1-Flt-1-Antibody-SY09-09-Immunohistochemistry-Paraffin-NBP3-11864-img0003.jpg)
![Flow Cytometry: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Flow cytometric analysis of A431 cells with NBP3-11864 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/VEGFR1-Flt-1-Antibody-SY09-09-Flow-Cytometry-NBP3-11864-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Immunocytochemistry staining VEGFR1/Flt-1 in N2A cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/VEGFR1-Flt-1-Antibody-SY09-09-Immunocytochemistry-Immunofluorescence-NBP3-11864-img0004.jpg)
![Immunocytochemistry/Immunofluorescence: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Immunocytochemistry staining VEGFR1/Flt-1 in RH-35 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.](http://images.novusbio.com/fullsize/VEGFR1-Flt-1-Antibody-SY09-09-Immunocytochemistry-Immunofluorescence-NBP3-11864-img0005.jpg)
![Immunohistochemistry-Paraffin: VEGFR1/Flt-1 Antibody (SY09-09) [NBP3-11864] - Immunohistochemical analysis of paraffin-embedded mouse placenta tissue using NBP3-11864. Counter stained with hematoxylin.](http://images.novusbio.com/fullsize/VEGFR1-Flt-1-Antibody-SY09-09-Immunohistochemistry-Paraffin-NBP3-11864-img0002.jpg)
![Western Blot: eIF4G1 [p Ser1231] Antibody [NBP1-04965] - Kinetics of eIF4G1 (s1232) phosphorylation in response to PKC/Ras/Erk activation by Sapintoxin D. Photo courtesy of a product review by the Gromeier Lab at Duke University.](http://images.novusbio.com/fullsize/eIF4G1-[p-Ser1231]-Antibody-Western-Blot-NBP1-04965-img0002.jpg "Western Blot: eIF4G1 [p Ser1231] Antibody [NBP1-04965] - Kinetics of eIF4G1 (s1232) phosphorylation in response to PKC/Ras/Erk activation by Sapintoxin D. Photo courtesy of a product review by the Gromeier Lab at Duke University.")
![<b>Biological Strategies Validation. </b>Western Blot: eIF4G1 [p Ser1231] Antibody [NBP1-04965] - HT29 cells untreated or treated with Anisomycin.](http://images.novusbio.com/fullsize/eIF4G1-[p-Ser1231]-Antibody-Western-Blot-NBP1-04965-img0003.jpg)
![Immunohistochemistry-Paraffin: eIF4G1 [p Ser1231] Antibody [NBP1-04965] - Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue using NBP1-04965 incubated with blocking peptide(right).](http://images.novusbio.com/fullsize/nbp1-04965_rabbit-polyclonal-eif4g1-p-ser1232-antibody-103202523464542.jpg)