| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26534-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26480-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26612-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26438-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26196-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26428-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26530-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26131-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26133-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-34730-0.1mg | |||
![Western Blot: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Positive Western Blot detected in: Hela whole cell lysate treated by 15mM sodium butyrate for 30min. All lanes: Histone H3.1 [ac Lys56] Antibody at 0.7ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.Predicted band size: 15 KDaObserved band size: 15 KDa](http://images.novusbio.com/fullsize/nbp3-26534_rabbit-histone-h3-1-ac-lys-56-mab-3h2-2822024114095.jpg "Western Blot: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Positive Western Blot detected in: Hela whole cell lysate treated by 15mM sodium butyrate for 30min. All lanes: Histone H3.1 [ac Lys56] Antibody at 0.7ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.Predicted band size: 15 KDaObserved band size: 15 KDa")
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Analysis of Histone H3.1 [ac Lys56] Antibody (3H2) diluted at 1:100 and staining in HepG2 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/nbp3-26534_rabbit-histone-h3-1-ac-lys-56-mab-3h2-282202412475119.jpg)
![Immunocytochemistry/Immunofluorescence: Histone H3.1 [ac Lys56] Antibody (3H2) [NBP3-26534] - Staining of Hela cells(treated by 15mM sodium butyrate for 30min) with Histone H3.1 [ac Lys56] Antibody (3H2) at 1:43, 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/nbp3-26534_rabbit-histone-h3-1-ac-lys-56-mab-3h2-28220241323621.jpg)
![Immunohistochemistry: bcl-x Antibody (5E9) [NBP3-26480] - Image of bcl-x Antibody (5E9) 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/nbp3-26480_rabbit-bcl-x-mab-5e9-2722024845329.jpg "Immunohistochemistry: bcl-x Antibody (5E9) [NBP3-26480] - Image of bcl-x Antibody (5E9) 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.")
![Western Blot: bcl-x Antibody (5E9) [NBP3-26480] - Positive Western Blot detected in: K562 whole cell lysate, Hela whole cell lysate, NIH/3T3 whole cell lysate, Rat Brain whole cell lysate, Mouse Brain whole cell lysate. All lanes: bcl-x Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 27, 19, 26 kDa Observed band size: 30 kDa](http://images.novusbio.com/fullsize/nbp3-26480_rabbit-bcl-x-mab-5e9-28220241144266.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: PTENP1 [p Ser29, p Thr32] Antibody [NBP1-77932] - Analysis of Rabbit Anti-Human IL-1 alpha Antibody. Lane 1: Opal Prestained Molecular Weight Ladder. Lane 2: IL-1 alpha 50ng. Lane 3: MEF WC lysate 10ng. Lane 4: MEF LPS stimulated 10ng. Blocking: BlockOut Buffer. Primary Antibody: Anti-IL-1a. Secondary Antibody: Goat anti-Rabbit HRP.](http://images.novusbio.com/fullsize/PTENP1-[p-Ser29--p-Thr32]-Antibody-Western-Blot-NBP1-77932-img0001.jpg "Western Blot: PTENP1 [p Ser29, p Thr32] Antibody [NBP1-77932] - Analysis of Rabbit Anti-Human IL-1 alpha Antibody. Lane 1: Opal Prestained Molecular Weight Ladder. Lane 2: IL-1 alpha 50ng. Lane 3: MEF WC lysate 10ng. Lane 4: MEF LPS stimulated 10ng. Blocking: BlockOut Buffer. Primary Antibody: Anti-IL-1a. Secondary Antibody: Goat anti-Rabbit HRP.")
![Immunoprecipitation: SHIP Antibody (9G11) [NBP3-26196] - Immunoprecipitating SHIP in Raji whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26196 in Raji whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26196 (2ug) + Raji whole cell lysate(500ug). Lane 3: Raji whole cell lysate (10ug).](http://images.novusbio.com/fullsize/nbp3-26196_rabbit-ship-mab-9g11-26220241322154.jpg "Immunoprecipitation: SHIP Antibody (9G11) [NBP3-26196] - Immunoprecipitating SHIP in Raji whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26196 in Raji whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26196 (2ug) + Raji whole cell lysate(500ug). Lane 3: Raji whole cell lysate (10ug).")
![Immunohistochemistry: SHIP Antibody (9G11) [NBP3-26196] - Image of SHIP Antibody (9G11) diluted at 1:100 and staining in paraffin-embedded human tonsil 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 IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26196_rabbit-ship-mab-9g11-272202485633.jpg)
![Western Blot: SHIP Antibody (9G11) [NBP3-26196] - Positive Western Blot detected in: Raji whole cell lysate, K562 whole cell lysate. All lanes: SHIP Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 134, 110 kDa Observed band size: 145 kDa](http://images.novusbio.com/fullsize/nbp3-26196_rabbit-ship-mab-9g11-282202411472145.jpg)
![Immunoprecipitation: CDK2 [p Tyr15] Antibody (2C4) [NBP3-26428] - Immunoprecipitating CDK2 [p Tyr15] in Hela whole cell lysate treated with Pervanadate.Lane 1: Rabbit control IgG (1ug)instead of NBP3-26428 in Hela whole cell lysate treated with Pervanadate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000).Lane 2: NBP3-26428 (3ug) + Hela whole cell lysate treated with Pervanadate (1mg).Lane 3: Hela whole cell lysate treated with Pervanadate (20ug).](http://images.novusbio.com/fullsize/nbp3-26428_rabbit-cdk2-p-tyr-15-mab-2c4-262202413221513.jpg "Immunoprecipitation: CDK2 [p Tyr15] Antibody (2C4) [NBP3-26428] - Immunoprecipitating CDK2 [p Tyr15] in Hela whole cell lysate treated with Pervanadate.Lane 1: Rabbit control IgG (1ug)instead of NBP3-26428 in Hela whole cell lysate treated with Pervanadate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000).Lane 2: NBP3-26428 (3ug) + Hela whole cell lysate treated with Pervanadate (1mg).Lane 3: Hela whole cell lysate treated with Pervanadate (20ug).")
![Western Blot: CDK2 [p Tyr15] Antibody (2C4) [NBP3-26428] - Positive Western Blot detected in: Hela whole cell lysate, 293 whole cell lysate (treated with Pervanadate or not). All lanes: CDK2 [p Tyr15] Antibody at 0.8ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution.Predicted band size: 34 KDaObserved band size: 34 KDa](http://images.novusbio.com/fullsize/nbp3-26428_rabbit-cdk2-p-tyr-15-mab-2c4-28220241140949.jpg)
![Immunocytochemistry/Immunofluorescence: CDK2 [p Tyr15] Antibody (2C4) [NBP3-26428] - Analysis of CDK2 [p Tyr15] Antibody (2C4) diluted at 1:80 and staining in Hela cells (treated with Pervanadate). The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and 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/nbp3-26428_rabbit-cdk2-p-tyr-15-mab-2c4-28220241312220.jpg)
![Western Blot: ATP Citrate Lyase Antibody (3A5) [NBP3-26530] - Positive Western Blot detected in: L02 whole cell lysate, K562 whole cell lysate, Hela whole cell lysate, Raji whole cell lysate, A549 whole cell lysate. All lanes: ATP Citrate Lyase Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 121, 120, 92 kDa Observed band size: 120 kDa](http://images.novusbio.com/fullsize/nbp3-26530_rabbit-atp-citrate-lyase-mab-3a5-282202411485810.jpg "Western Blot: ATP Citrate Lyase Antibody (3A5) [NBP3-26530] - Positive Western Blot detected in: L02 whole cell lysate, K562 whole cell lysate, Hela whole cell lysate, Raji whole cell lysate, A549 whole cell lysate. All lanes: ATP Citrate Lyase Antibody at 1: 1500 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 121, 120, 92 kDa Observed band size: 120 kDa")
![Immunocytochemistry/Immunofluorescence: ATP Citrate Lyase Antibody (3A5) [NBP3-26530] - Staining of HepG2 Cells with ATP Citrate Lyase Antibody (3A5) at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% Triton X-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26530_rabbit-atp-citrate-lyase-mab-3a5-28220241312231.jpg)
![Flow Cytometry: ATP Citrate Lyase Antibody (3A5) [NBP3-26530] - Overlay histogram showing Hela cells stained with ATP Citrate Lyase Antibody (3A5) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10^6 cells) for 1 h at 4C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min 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/nbp3-26530_rabbit-atp-citrate-lyase-mab-3a5-282202414183647.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](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-Paraffin: Phospho-Tyrosine Antibody (PY793) [NBP2-45213] - Human Breast Carcinoma stained with Phosphotyrosine Monoclonal Antibody (PY793).](http://images.novusbio.com/fullsize/Phospho-Tyrosine-Antibody-PY793-Immunohistochemistry-Paraffin-NBP2-45213-img0001.jpg "Immunohistochemistry-Paraffin: Phospho-Tyrosine Antibody (PY793) [NBP2-45213] - Human Breast Carcinoma stained with Phosphotyrosine Monoclonal Antibody (PY793).")