| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26658-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26486-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26296-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26624-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| IHC-Prediluted | NBP2-44406 | |||
| Azide and BSA Free | NBP2-34552-0.1mg | |||
![Western Blot: NEK2 Antibody [NBP1-78022] - Western blot analysis is shown using Affinity Purified NEK2 antibody to detect enCanineenous protein present in an unstimulated mouse A-20 whole cell lysate (arrowhead). Comparison to a molecular weight marker indicates a band of ~52 kDa correspond-ing to NEK2 protein. The blot was incubated with a 1:500 dilution of the antibody at room temperature followed by detection using standard techniques.](http://images.novusbio.com/fullsize/NEK2-Antibody-Western-Blot-NBP1-78022-img0005.jpg "Western Blot: NEK2 Antibody [NBP1-78022] - Western blot analysis is shown using Affinity Purified NEK2 antibody to detect enCanineenous protein present in an unstimulated mouse A-20 whole cell lysate (arrowhead). Comparison to a molecular weight marker indicates a band of ~52 kDa correspond-ing to NEK2 protein. The blot was incubated with a 1:500 dilution of the antibody at room temperature followed by detection using standard techniques.")
![Western Blot: NEK2 Antibody [NBP1-78022] - Western Blot of NEK2 antibody. Lane 1: Opal Pre-stained Molecular Weight Marker. Lane 2: Jurkat cell lysate (10ug) spiked with rec. NEK2 protein (50ng). Lane 3: Jurkat cell lysate (10ug) spiked with rec. NEK2 protein (20ng). Lane 4: Jurkat cell lysate (10ug) spiked with rec. NEK2 protein (20ng). Lane 5: Jurkat cell lysate (10ug). Primary Antibody: Anti-NEK2 at 1ug/mL overnight at 2-8C. Secondary Antibody: Goat Anti-Rabbit IgG HRP at 1:70,000 for 30mins at RT. Block: BlockOut Buffer. Expect/Observed MW: ~76kDa rec NEK2.](http://images.novusbio.com/fullsize/NEK2-Antibody-Western-Blot-NBP1-78022-img0004.jpg)
![N/A: NEK2 Antibody [NBP1-78022]](http://images.novusbio.com/fullsize/NEK2-Antibody-N-A-NBP1-78022-img0003.jpg)
![Immunohistochemistry: Chk1 Antibody (2F2) [NBP3-26658] - Image of Chk1 Antibody (2F2) diluted at 1:100 and staining in paraffin-embedded human small intestine 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/nbp3-26658_rabbit-chk1-mab-2f2-26220241510613.jpg "Immunohistochemistry: Chk1 Antibody (2F2) [NBP3-26658] - Image of Chk1 Antibody (2F2) diluted at 1:100 and staining in paraffin-embedded human small intestine 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.")
![Western Blot: Chk1 Antibody (2F2) [NBP3-26658] - Positive Western Blot detected in: K562 whole cell lysate, 293T whole cell lysate, MCF-7 whole cell lysate, HepG2 whole cell lysate. All lanes: Chk1 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 55, 44, 51 kDa Observed band size: 55 kDa](http://images.novusbio.com/fullsize/nbp3-26658_rabbit-chk1-mab-2f2-282202411442640.jpg)
![Immunocytochemistry/Immunofluorescence: Chk1 Antibody (2F2) [NBP3-26658] - Staining of Hela Cells with Chk1 Antibody (2F2) 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/nbp3-26658_rabbit-chk1-mab-2f2-28220241323640.jpg)
![Immunoprecipitation: Aurora B Antibody (4E5) [NBP3-26486] - Immunoprecipitating Aurora B in Hela whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26486 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26486 (2ug) + Hela whole cell lysate (500ug). Lane 3: Hela whole cell lysate (10ug).](http://images.novusbio.com/fullsize/nbp3-26486_rabbit-aurora-b-mab-4e5-26220241322158.jpg "Immunoprecipitation: Aurora B Antibody (4E5) [NBP3-26486] - Immunoprecipitating Aurora B in Hela whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26486 in Hela whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26486 (2ug) + Hela whole cell lysate (500ug). Lane 3: Hela whole cell lysate (10ug).")
![Immunohistochemistry: Aurora B Antibody (4E5) [NBP3-26486] - Image of Aurora B Antibody (4E5) 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/nbp3-26486_rabbit-aurora-b-mab-4e5-262202415253321.jpg)
![Immunohistochemistry: Aurora B Antibody (4E5) [NBP3-26486] - Image of Aurora B Antibody (4E5) 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/nbp3-26486_rabbit-aurora-b-mab-4e5-2722024827492.jpg)
![Western Blot: Aurora B Antibody (4E5) [NBP3-26486] - Positive Western Blot detected in: Hela whole cell lysate, Jurkat whole cell lysate, 293 whole cell lysate, MCF-7 whole cell lysate, U251 whole cell lysate, A549 whole cell lysate, HepG2 whole cell lysate. All lanes: Aurora B Antibody at 1: 2000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 40, 36, 17, 35 kDa Observed band size: 40 kDa](http://images.novusbio.com/fullsize/nbp3-26486_rabbit-aurora-b-mab-4e5-282202411442635.jpg)
![Western Blot: MCM3 Antibody [NB100-249] - Samples: Whole cell lysate (50 ug) from HeLa and 293T cells prepared using NETN lysis buffer. Antibody: Affinity purified goat anti-MCM3 antibody used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/MCM3-Antibody-Western-Blot-NB100-249-img0059.jpg "<b>Biological Strategies Validation. </b>Western Blot: MCM3 Antibody [NB100-249] - Samples: Whole cell lysate (50 ug) from HeLa and 293T cells prepared using NETN lysis buffer. Antibody: Affinity purified goat anti-MCM3 antibody used for WB at 0.1 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry: MCM3 Antibody [NB100-249] - Sample: FFPE section of human colon carcinoma. Antibody: Affinity purified goat anti-MCM3 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB](http://images.novusbio.com/fullsize/MCM3-Antibody-Immunohistochemistry-NB100-249-img0061.jpg)
![Western Blot: MCM3 Antibody [NB100-249] - Whole cell lysate (60 ug) from HeLa cells. Antibody used at 0.25 ug/ml.](http://images.novusbio.com/fullsize/MCM3-Antibody-Western-Blot-NB100-249-img0002.jpg)
![Immunoprecipitation: SUMO1 Antibody (5G3) [NBP3-26296] - Immunoprecipitating SUMO1 in 293T whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26296 in 293T whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26296 (3ug) + 293T whole cell lysate (500ug). Lane 3: 293T whole cell lysate (20ug).](http://images.novusbio.com/fullsize/nbp3-26296_rabbit-sumo1-mab-5g3-262202413221515.jpg "Immunoprecipitation: SUMO1 Antibody (5G3) [NBP3-26296] - Immunoprecipitating SUMO1 in 293T whole cell lysate. Lane 1: Rabbit control IgG instead of NBP3-26296 in 293T whole cell lysate. For western blotting, a HRP-conjugated Protein G antibody was used as the secondary antibody (1/2000). Lane 2: NBP3-26296 (3ug) + 293T whole cell lysate (500ug). Lane 3: 293T whole cell lysate (20ug).")
![Immunohistochemistry: SUMO1 Antibody (5G3) [NBP3-26296] - Image of SUMO1 Antibody (5G3) diluted at 1:92.5 and staining in paraffin-embedded human adrenal gland 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26296_rabbit-sumo1-mab-5g3-262202415475623.jpg)
![Immunohistochemistry: SUMO1 Antibody (5G3) [NBP3-26296] - Image of SUMO1 Antibody (5G3) diluted at 1:92.5 and staining in paraffin-embedded human adrenal gland 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 biotinylated secondary antibody and visualized using an HRP conjugated SP system.](http://images.novusbio.com/fullsize/nbp3-26296_rabbit-sumo1-mab-5g3-26220241525334.jpg)
![Flow Cytometry: SUMO1 Antibody (5G3) [NBP3-26296] - Overlay histogram showing Hela cells stained with SUMO1 Antibody (5G3) (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4C. Control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/nbp3-26296_rabbit-sumo1-mab-5g3-282202414312781.jpg)
![Western Blot: integrin beta 4 binding protein Antibody [NBP1-52640] - Affinity purified rabbit anti-eIF6 antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 6 mcg/mg lysate. eIF6 was also immunoprecipitated by rabbit anti-eIF6 antibody NBP1-52641, which recognizes a downstream epitope.](http://images.novusbio.com/fullsize/integrin-beta-4-binding-protein-Antibody-Western-Blot-NBP1-52640-img0001.jpg "<b>Independent Antibodies Validation. </b>Western Blot: integrin beta 4 binding protein Antibody [NBP1-52640] - Affinity purified rabbit anti-eIF6 antibody used for WB at 0.1 mcg/ml (A) and 1 mcg/ml (B) and used for IP at 6 mcg/mg lysate. eIF6 was also immunoprecipitated by rabbit anti-eIF6 antibody NBP1-52641, which recognizes a downstream epitope.")
![<b>Independent Antibodies Validation. </b>Immunohistochemistry: integrin beta 4 binding protein Antibody [NBP1-52640] - Samples: FFPE serial sections of mouse renal cell carcinoma. Antibody: Affinity purified rabbit anti- eIF6 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB. Counterstain: Hematoxylin (blue).](http://images.novusbio.com/fullsize/integrin-beta-4-binding-protein-Antibody-Immunohistochemistry-NBP1-52640-img0003.jpg)
![Immunohistochemistry: integrin beta 4 binding protein Antibody [NBP1-52640] - Samples: FFPE serial sections of human ovarian carcinoma. Antibody: Affinity purified rabbit anti- eIF6 used at a dilution of 1:1,000 (1ug/ml). Detection: DAB. Counterstain: Hematoxylin (blue).](http://images.novusbio.com/fullsize/integrin-beta-4-binding-protein-Antibody-Immunohistochemistry-NBP1-52640-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: UbcH3/Cdc34 Antibody [NBP1-32153] - HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: CDC34 protein stained by CDC34 antibody [N1C3] diluted at 1:200. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [B-5-1-2] diluted at 1:10000. Blue: Hoechst 33342 staining.](http://images.novusbio.com/fullsize/UbcH3-Cdc34-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32153-img0007.jpg "Immunocytochemistry/Immunofluorescence: UbcH3/Cdc34 Antibody [NBP1-32153] - HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: CDC34 protein stained by CDC34 antibody [N1C3] diluted at 1:200. Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [B-5-1-2] diluted at 1:10000. Blue: Hoechst 33342 staining.")
![Immunocytochemistry/Immunofluorescence: UbcH3/Cdc34 Antibody [NBP1-32153] - Paraformaldehyde-fixed A549, using antibody at 1:200 dilution.](http://images.novusbio.com/fullsize/UbcH3-Cdc34-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-32153-img0004.jpg)
![UbcH3/Cdc34 Antibody [NBP1-32153] -Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with CDC34 antibody [N1C3] 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/nbp1-32153_rabbit-polyclonal-ube2r1-cdc34-antibody-western-blot-152023124356..jpg)
![Western Blot: Enolase 1 Antibody (2217) [NBP2-43702] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with ENO1 antibody diluted at 1:10000. HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Enolase-1-Antibody-2217-Western-Blot-NBP2-43702-img0004.jpg "Western Blot: Enolase 1 Antibody (2217) [NBP2-43702] - Various whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with ENO1 antibody diluted at 1:10000. HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.")
![Western Blot: Enolase 1 Antibody (2217) [NBP2-43702] - Analysis of A. 30 ug A549 whole cell lysate/extract B. 30 ug H1299 whole cell lysate/extract C. 30 ug HCT116 whole cell lysate/extract 10 % SDS-PAGE ENO1 antibody [2217] dilution: 1:10000.](http://images.novusbio.com/fullsize/Enolase-1-Antibody-2217-Western-Blot-NBP2-43702-img0001.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: Enolase 1 Antibody (2217) [NBP2-43702] - Non-transfected (-) and transfected (+) 293T whole cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with ENO1 antibody [2217].](http://images.novusbio.com/fullsize/Enolase-1-Antibody-2217-Western-Blot-NBP2-43702-img0002.jpg)
![Western Blot: Enolase 1 Antibody (2217) [NBP2-43702] - Rat tissue extract (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with ENO1 antibody diluted at 1:10000. HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Enolase-1-Antibody-2217-Western-Blot-NBP2-43702-img0003.jpg)
![Immunohistochemistry: DEK Antibody (20D2) [NBP3-26624] - Image of DEK Antibody (20D2) diluted at 1:50 and staining in paraffin-embedded human gastric 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 polymer IgG labeled by HRP and visualized using 0.67% DAB.](http://images.novusbio.com/fullsize/nbp3-26624_rabbit-dek-mab-20d2-26220241535572.jpg "Immunohistochemistry: DEK Antibody (20D2) [NBP3-26624] - Image of DEK Antibody (20D2) diluted at 1:50 and staining in paraffin-embedded human gastric 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 polymer IgG labeled by HRP and visualized using 0.67% DAB.")
![Immunohistochemistry: DEK Antibody (20D2) [NBP3-26624] - Image of DEK Antibody (20D2) diluted at 1:50 and staining in paraffin-embedded human gastric 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 0.67% DAB.](http://images.novusbio.com/fullsize/nbp3-26624_rabbit-dek-mab-20d2-27220248453215.jpg)
![Immunocytochemistry/Immunofluorescence: DEK Antibody (20D2) [NBP3-26624] - Staining of Hela with DEK Antibody (20D2) at 1:20, 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 524-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26624_rabbit-dek-mab-20d2-28220241323612.jpg)
![Flow Cytometry: DEK Antibody (20D2) [NBP3-26624] - Overlay Peak curve showing Hela cells stained with DEK Antibody (20D2) (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/nbp3-26624_rabbit-dek-mab-20d2-282202414183679.jpg)
![Western Blot: Chk1 [p Ser317] Antibody [NBP2-37703] - Whole cell lysate (50 ug) from HeLa cells prepared using NETN lysis buffer treated with hydroxyurea (2mM for 24 hours), EPE (100uM for 4 hours), or untreated. Affinity purified rabbit anti-Chk1, Phospho (S317) antibody used for WB at 0.2 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.](http://images.novusbio.com/fullsize/Chk1-[p-Ser317]-Antibody-Western-Blot-NBP2-37703-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: Chk1 [p Ser317] Antibody [NBP2-37703] - Whole cell lysate (50 ug) from HeLa cells prepared using NETN lysis buffer treated with hydroxyurea (2mM for 24 hours), EPE (100uM for 4 hours), or untreated. Affinity purified rabbit anti-Chk1, Phospho (S317) antibody used for WB at 0.2 ug/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry: Chk1 [p Ser317] Antibody [NBP2-37703] - Sample: FFPE section of human breast carcinoma. Antibody: Affinity purified rabbit anti- Chk1, Phospho (S317) used at a dilution of 1:1,000 (1ug/ml). Detection: DAB. Counterstain: IHC Hematoxylin (blue).](http://images.novusbio.com/fullsize/Chk1-[p-Ser317]-Antibody-Immunohistochemistry-NBP2-37703-img0003.jpg)
![Immunohistochemistry-Paraffin: Cdc20 Antibody (AR12) [NBP2-32954] - Formalin-fixed, paraffin-embedded human Tonsil stained with Cdc20 Antibody (AR12).](http://images.novusbio.com/fullsize/Cdc20-Antibody-AR12-Immunohistochemistry-Paraffin-NBP2-32954-img0003.jpg "Immunohistochemistry-Paraffin: Cdc20 Antibody (AR12) [NBP2-32954] - Formalin-fixed, paraffin-embedded human Tonsil stained with Cdc20 Antibody (AR12).")
![Immunohistochemistry-Paraffin: Cdc20 Antibody (AR12) [NBP2-32954] - Formalin-fixed, paraffin-embedded human Gastric Carcinoma stained with Cdc20 Antibody (AR12).](http://images.novusbio.com/fullsize/Cdc20-Antibody-AR12-Immunohistochemistry-Paraffin-NBP2-32954-img0002.jpg)
![Immunohistochemistry: POLR3K Antibody - BSA Free [NBP3-46938] - Immunohistochemistry of paraffin-embedded human gliomas using (POLR3K antibody) at dilution of 1:100](http://images.novusbio.com/fullsize/nbp3-46938_rabbit-polr3k-pab-bsa-free-28420251235640.jpg "Immunohistochemistry: POLR3K Antibody - BSA Free [NBP3-46938] - Immunohistochemistry of paraffin-embedded human gliomas using (POLR3K antibody) at dilution of 1:100")
![Western Blot: POLR3K Antibody - BSA Free [NBP3-46938] - Transfected HEK-293 cells were subjected to SDS PAGE followed by western blot with (POLR3K Antibody) at dilution of 1:1000](http://images.novusbio.com/fullsize/nbp3-46938_rabbit-polr3k-pab-bsa-free-28420251231212.jpg)