| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26131-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26133-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26514-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26300-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26152-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26612-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26438-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26394-50ul | |||
![Western Blot: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. All lanes: Histone H3.1 [Monomethyl Arg17] Antibody at 1.55ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26131_rabbit-histone-h3-1-monomethyl-arg-17-mab-3e10-282202411472138.jpg "Western Blot: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Positive Western Blot detected in Hela whole cell lysate. HepG2 whole cell lysate. SH-SY5Y whole cell lysate. All lanes: Histone H3.1 [Monomethyl Arg17] Antibody at 1.55ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Staining of Hela cells withHistone H3.1 [Monomethyl Arg17] Antibody (3E10) at 1:96, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26131_rabbit-histone-h3-1-monomethyl-arg-17-mab-3e10-28220241312210.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Arg17] Antibody (3E10) [NBP3-26131] - Analysis of Histone H3.1 [Monomethyl Arg17] Antibody (3E10) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26131_rabbit-histone-h3-1-monomethyl-arg-17-mab-3e10-282202412475141.jpg)
![Western Blot: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Positive Western Blot detected in HepG2 whole cell lysate. SH-SY5Y whole cell lysate. Rat brain tissue. All lanes: Histone H3.1 [Monomethyl Lys36] Antibody at 0.6ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26133_rabbit-histone-h3-1-monomethyl-lys-36-mab-1f4-28220241148583.jpg "Western Blot: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Positive Western Blot detected in HepG2 whole cell lysate. SH-SY5Y whole cell lysate. Rat brain tissue. All lanes: Histone H3.1 [Monomethyl Lys36] Antibody at 0.6ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 15 KDa Observed band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Staining of Hela cells with Histone H3.1 [Monomethyl Lys36] Antibody (1F4) at 1:37.5, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26133_rabbit-histone-h3-1-monomethyl-lys-36-mab-1f4-282202412475136.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [Monomethyl Lys36] Antibody (1F4) [NBP3-26133] - Analysis of Histone H3.1 [Monomethyl Lys36] Antibody (1F4) diluted at 1:100 and staining in Hela cells. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26133_rabbit-histone-h3-1-monomethyl-lys-36-mab-1f4-282202412493646.jpg)
![Immunohistochemistry: AKT1/2/3 Antibody (16E10) [NBP3-26514] - Image of AKT1/2/3 Antibody (16E10) diluted at 1:50 and staining in paraffin-embedded human brain tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.54% DAB.](http://images.novusbio.com/fullsize/nbp3-26514_rabbit-akt1-2-3-mab-16e10-2722024847194.jpg "Immunohistochemistry: AKT1/2/3 Antibody (16E10) [NBP3-26514] - Image of AKT1/2/3 Antibody (16E10) diluted at 1:50 and staining in paraffin-embedded human brain tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.54% DAB.")
![Western Blot: AKT1/2/3 Antibody (16E10) [NBP3-26514] - Positive Western Blot detected in: SH-SY5Y whole cell lysate. All lanes: AKT1/2/3 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 56 kDa Observed band size: 56 kDa](http://images.novusbio.com/fullsize/nbp3-26514_rabbit-akt1-2-3-mab-16e10-282202411442636.jpg)
![Flow Cytometry: AKT1/2/3 Antibody (16E10) [NBP3-26514] - Overlay Peak curve showing Jurkat cells stained with AKT1/2/3 Antibody (16E10) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26514_rabbit-akt1-2-3-mab-16e10-28220241418367.jpg)
![Immunohistochemistry: STAT4 Antibody (26G2) [NBP3-26300] - Image of STAT4 Antibody (26G2) diluted at 1:100 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26300_rabbit-stat4-mab-26g2-262202415355717.jpg "Immunohistochemistry: STAT4 Antibody (26G2) [NBP3-26300] - Image of STAT4 Antibody (26G2) diluted at 1:100 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: STAT4 Antibody (26G2) [NBP3-26300] - Image of STAT4 Antibody (26G2) diluted at 1:100 and staining in paraffin-embedded human testis tissue performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26300_rabbit-stat4-mab-26g2-27220248504614.jpg)
![Immunocytochemistry/Immunofluorescence: STAT4 Antibody (26G2) [NBP3-26300] - Staining of HepG2 cell with STAT4 Antibody (26G2) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 515-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26300_rabbit-stat4-mab-26g2-282202412475120.jpg)
![Immunoprecipitation: MEK1 Antibody (3F10) [NBP3-26152] - Immunoprecipitating MEK1 in Hela whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26152 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26152 (2ug) + Hela whole cell lysate (500ug). Lane 3: Hela whole cell lysate (10ug).](http://images.novusbio.com/fullsize/nbp3-26152_rabbit-mek1-mab-3f10-2622024132373.jpg "Immunoprecipitation: MEK1 Antibody (3F10) [NBP3-26152] - Immunoprecipitating MEK1 in Hela whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26152 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26152 (2ug) + Hela whole cell lysate (500ug). Lane 3: Hela whole cell lysate (10ug).")
![Immunohistochemistry: MEK1 Antibody (3F10) [NBP3-26152] - Image of MEK1 Antibody (3F10) diluted at 1:100 and staining in paraffin-embedded human colon cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26152_rabbit-mek1-mab-3f10-27220248573314.jpg)
![Western Blot: MEK1 Antibody (3F10) [NBP3-26152] - Positive Western Blot detected in: Hela whole cell lysate, 293 whole cell lysate, A549 whole cell lysate, U87 whole cell lysate. All lanes: MEK1 Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 44, 41 kDa Observed band size: 44 kDa](http://images.novusbio.com/fullsize/nbp3-26152_rabbit-mek1-mab-3f10-2822024114090.jpg)
![Western Blot: STAT5a [p Tyr694] Antibody [NBP1-77851] - shows detection of phosphorylated Stat5 (indicated by arrowhead at ~91 kDa) in NK92 cells after 30 min treatment with 1Ku of IL-2 (lane 2). No reactivity is seen for non-phosphorylated Stat5 in untreated cells (lane 1). The membrane was probed with the primary antibody at a 1:1,000 dilution, overnight at 4C.](http://images.novusbio.com/fullsize/STAT5a-[p-Tyr694]-Antibody-Western-Blot-NBP1-77851-img0002.jpg "Western Blot: STAT5a [p Tyr694] Antibody [NBP1-77851] - shows detection of phosphorylated Stat5 (indicated by arrowhead at ~91 kDa) in NK92 cells after 30 min treatment with 1Ku of IL-2 (lane 2). No reactivity is seen for non-phosphorylated Stat5 in untreated cells (lane 1). The membrane was probed with the primary antibody at a 1:1,000 dilution, overnight at 4C.")
![Immunohistochemistry: STAT5a [p Tyr694] Antibody [NBP1-77851] - Used at 20g/ml to detect signal in a variety of tissues including multi-human, multi-brain and multi-cancer slides. This image shows moderate positive staining of distal convoluted tubules and collecting ducts of human kidney at 40X. Tissue was formalin-fixed and paraffin embedded. The image shows localization of the antibody as the precipitated red signal, with a hematoxylin purple nuclear counterstain.](http://images.novusbio.com/fullsize/STAT5a-[p-Tyr694]-Antibody-Immunohistochemistry-NBP1-77851-img0003.jpg)
![Flow Cytometry: ZAP70 [p Tyr319] Antibody [NBP1-18896] - Flow cytometric analysis of phospho-Zap70 (Y319). Jurkat cells were treated with H2O2 for 3 minutes. Cells were fixed in 1.5% PFA, permeabilized in 90%, and 1 X 10e6 cells stained with 1.0 mcg/ml Phospho Zap70 (Y319) antibody in a 150 mcl volume. Isotype anti-KLH control (black) in H2O2 treated cells, anti-phospho Zap70 (Y319) in untreated cells (red), antiphospho Zap70 (Y319) in H2O2 treated (blue).](http://images.novusbio.com/fullsize/ZAP70-[p-Tyr319]-Antibody-Flow-Cytometry-NBP1-18896-img0001.jpg "Flow Cytometry: ZAP70 [p Tyr319] Antibody [NBP1-18896] - Flow cytometric analysis of phospho-Zap70 (Y319). Jurkat cells were treated with H2O2 for 3 minutes. Cells were fixed in 1.5% PFA, permeabilized in 90%, and 1 X 10e6 cells stained with 1.0 mcg/ml Phospho Zap70 (Y319) antibody in a 150 mcl volume. Isotype anti-KLH control (black) in H2O2 treated cells, anti-phospho Zap70 (Y319) in untreated cells (red), antiphospho Zap70 (Y319) in H2O2 treated (blue).")
![Immunoprecipitation: ZAP70 [p Tyr319] Antibody [NBP1-18896] - Whole cell lysate from Jurkat cells that had been treated with hydrogen peroxide. ZAP70 antibodies NBP1-18896, NBP1-1889, and NBP1-18898 used for IP at 3 mcg/mg lysate.](http://images.novusbio.com/fullsize/ZAP70-[p-Tyr319]-Antibody-Immunoprecipitation-NBP1-18896-img0004.jpg)
![Immunoprecipitation: ZAP70 [p Tyr319] Antibody [NBP1-18896] - Jurkat WC Lysate treated with hydrogen peroxide (+) or mock treated (-). NB100-97826 was used to IP ZAP70. The IPs were either treated with phosphatase (+) or mock (-) treated.](http://images.novusbio.com/fullsize/ZAP70-[p-Tyr319]-Antibody-Immunoprecipitation-NBP1-18896-img0005.jpg)
![Immunohistochemistry: CRMP2 Antibody (20D8) [NBP3-26612] - Image of CRMP2 Antibody (20D8) diluted at 1:50 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.35% DAB.](http://images.novusbio.com/fullsize/nbp3-26612_rabbit-crmp2-mab-20d8-262202414471542.jpg "Immunohistochemistry: CRMP2 Antibody (20D8) [NBP3-26612] - Image of CRMP2 Antibody (20D8) diluted at 1:50 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.35% DAB.")
![Immunocytochemistry/Immunofluorescence: CRMP2 Antibody (20D8) [NBP3-26612] - Staining of SH-SY5Y with CRMP2 Antibody (20D8) at 1:25, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 506-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26612_rabbit-crmp2-mab-20d8-282202412493633.jpg)
![Flow Cytometry: CRMP2 Antibody (20D8) [NBP3-26612] - Overlay Peak curve showing SH-SY5Y cells stained with CRMP2 Antibody (20D8) (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% Triton X-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 45min at 4C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4C. Control antibody (green line) was rabbit IgG (1ug/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26612_rabbit-crmp2-mab-20d8-282202414183684.jpg)
![Immunohistochemistry: PARP Antibody (7C11) [NBP3-26438] - Image of PARP Antibody (7C11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26438_rabbit-parp-mab-7c11-262202415355711.jpg "Immunohistochemistry: PARP Antibody (7C11) [NBP3-26438] - Image of PARP Antibody (7C11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: PARP Antibody (7C11) [NBP3-26438] - Image of PARP Antibody (7C11) diluted at 1:100 and staining in paraffin-embedded human breast cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26438_rabbit-parp-mab-7c11-272202485637.jpg)
![Western Blot: PARP Antibody (7C11) [NBP3-26438] - Positive Western Blot detected in: K562 whole cell lysate. All lanes: PARP Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 114 kDa Observed band size: 114 kDa](http://images.novusbio.com/fullsize/nbp3-26438_rabbit-parp-mab-7c11-282202411472110.jpg)
![Western Blot: PLA2G4A Antibody (C19) [NBP3-41481] - Sample: Recombinant PLA2G4A, Human.](http://images.novusbio.com/fullsize/nbp3-41481_mouse-pla2g4a-mab-c19-612202421331651.jpg "Western Blot: PLA2G4A Antibody (C19) [NBP3-41481] - Sample: Recombinant PLA2G4A, Human.")
![Western Blot: PLA2G4A Antibody (C19) [NBP3-41481] - Sample: Human Lung lysate Primary Ab: 1ug/ml NBP3-41481; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41481_mouse-pla2g4a-mab-c19-612202420484711.jpg)
![Western Blot: PLA2G4A Antibody (C19) [NBP3-41481] - Sample: Hela cell lysate Primary Ab: 1ug/ml NBP3-41481; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41481_mouse-pla2g4a-mab-c19-612202420484716.jpg)
![Immunoprecipitation: RSK1 [p Thr359, p Ser363] Antibody (1B6) [NBP3-26394] - Immunoprecipitating RSK1 [p Thr359, p Ser363] in Hela whole cell lysate. Lane 1: Rabbit control IgG (1ug) instead of NBP3-26394 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26394 (3ug) + Hela whole cell lysate (1mg). Lane 3: Hela whole cell lysate (20ug).](http://images.novusbio.com/fullsize/nbp3-26394_rabbit-rsk1-p-thr-359-p-ser-363-mab-1b6-262202413221523.jpg "Immunoprecipitation: RSK1 [p Thr359, p Ser363] Antibody (1B6) [NBP3-26394] - Immunoprecipitating RSK1 [p Thr359, p Ser363] in Hela whole cell lysate. Lane 1: Rabbit control IgG (1ug) instead of NBP3-26394 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26394 (3ug) + Hela whole cell lysate (1mg). Lane 3: Hela whole cell lysate (20ug).")
![Western Blot: RSK1 [p Thr359, p Ser363] Antibody (1B6) [NBP3-26394] - Positive Western Blot detected in HepG2 whole cell lysate (treated with EGF or not). All lanes: RSK1 [p Thr359, p Ser363] Antibody at 0.69ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 90 KDa Observed band size: 90 KDa](http://images.novusbio.com/fullsize/nbp3-26394_rabbit-rsk1-p-thr-359-p-ser-363-mab-1b6-28220241141366.jpg)
![Immunocytochemistry/Immunofluorescence: RSK1 [p Thr359, p Ser363] Antibody (1B6) [NBP3-26394] - Staining of Hela cells with RSK1 [p Thr359, p Ser363] Antibody (1B6) at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26394_rabbit-rsk1-p-thr-359-p-ser-363-mab-1b6-2822024131220.jpg)