| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90081-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99774-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-00079-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98832-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98838-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98881-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98775-50ul | |||
![Western Blot: eIF4G1 [p Ser1108] Antibody (PS01-08) [NBP3-32764] - Western blot analysis of eIF4G1 on different lysates with Rabbit anti-eIF4G1 antibody (NBP3-32764) at 1/1,000 dilution.<br/><br/> Lane 1: A431 cell lysate<br/> Lane 2: SK-Br-3 cell lysate<br/> Lane 3: MCF-7 cell lysate<br/><br/> Lysates/proteins at 10 ug/Lane.<br/><br/> Predicted band size: 175 kDa<br/> Observed band size: 250 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 6% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32764) 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 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32764_rabbit-eif4g1-p-ser1108-mab-ps01-08-288202412442973.jpg "Western Blot: eIF4G1 [p Ser1108] Antibody (PS01-08) [NBP3-32764] - Western blot analysis of eIF4G1 on different lysates with Rabbit anti-eIF4G1 antibody (NBP3-32764) at 1/1,000 dilution.<br/><br/> Lane 1: A431 cell lysate<br/> Lane 2: SK-Br-3 cell lysate<br/> Lane 3: MCF-7 cell lysate<br/><br/> Lysates/proteins at 10 ug/Lane.<br/><br/> Predicted band size: 175 kDa<br/> Observed band size: 250 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 6% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32764) 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 1:300,000 dilution was used for 1 hour at room temperature.")
![Immunocytochemistry/ Immunofluorescence: eIF4G1 [p Ser1108] Antibody (PS01-08) [NBP3-32764] - Immunocytochemistry analysis of A431 cells labeling eIF4G1 with Rabbit anti-eIF4G1 antibody (NBP3-32764) at 1/50 dilution.<br/><br/> Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-eIF4G1 antibody (NBP3-32764) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.](http://images.novusbio.com/fullsize/nbp3-32764_rabbit-eif4g1-p-ser1108-mab-ps01-08-29202410484829.jpg)
![Western blot analysis on different lysates with NBP3-32764 at 1/1,000 dilution. Lane 1: HEK-293 (Human embryonic kidney cell) cell lysate Lysates/proteins at 20 µg/Lane. Exposure time: 1 minutes Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: NBP3-32764, 1/1,000 in 5% NFDM/TBST, overnight at 4 ℃ Secondary antibody: Goat Anti-Rabbit IgG [HRP] Secondary Antibody, 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 175.5 kDa Observed band size: 250 kDa](http://images.novusbio.com/fullsize/nbp3-32764_-western-blot-639204594553515792.jpg)
![Western Blot: PNK Antibody (JE64-85) [NBP3-32836] - Western blot analysis of PNK on different lysates with Rabbit anti-PNK antibody (NBP3-32836) at 1/500 dilution.<br/><br/> Lane 1: HepG2 cell lysate<br/> Lane 2: 293 cell lysate<br/> Lane 3: PC-3 cell lysate<br/> Lane 4: Jurkat cell lysate<br/><br/> Lysates/proteins at 10 ug/Lane.<br/><br/> Predicted band size: 57 kDa<br/> Observed band size: 60 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 10% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32836) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32836_rabbit-pnk-mab-je64-85-288202412442925.jpg "Western Blot: PNK Antibody (JE64-85) [NBP3-32836] - Western blot analysis of PNK on different lysates with Rabbit anti-PNK antibody (NBP3-32836) at 1/500 dilution.<br/><br/> Lane 1: HepG2 cell lysate<br/> Lane 2: 293 cell lysate<br/> Lane 3: PC-3 cell lysate<br/> Lane 4: Jurkat cell lysate<br/><br/> Lysates/proteins at 10 ug/Lane.<br/><br/> Predicted band size: 57 kDa<br/> Observed band size: 60 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 10% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32836) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: PNK Antibody (JE64-85) [NBP3-32836] - Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue with Rabbit anti-PNK antibody (NBP3-32836) at 1/100 dilution.<br/><br/> The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32836) at 1/100 dilution for 1 hour 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/nbp3-32836_rabbit-pnk-mab-je64-85-298202413585524.jpg)
![Western blot analysis on different lysates with NBP3-32836 at 1/5,000 dilution. Lane 1: HepG2 (Human liver cancer cell) cell lysate Lane 2: Jurkat (Human T-lymphoblastic cells) cell lysate Lane 3: A549 (Human lung adenocarcinoma cell) cell lysate Lane4: Hela (Human cervical adenocarcinoma cell) cell lysate Lysates/proteins at 20 µg/Lane. Exposure time: 3 minutes Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: NBP3-32836, 1/5,000 in primary antibody dilution buffer, overnight at 4 ℃ Secondary antibody: Goat Anti-Rabbit IgG [HRP] Secondary Antibody, 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 57.1 kDa Observed band size: 60 kDa](http://images.novusbio.com/fullsize/nbp3-32836_-western-blot-639204594548227888.jpg)
![Immunohistochemistry-Paraffin: HSF1 Antibody (009) [NBP2-90081] - Staining of human HSF1 in human tonsil with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/HSF1-Antibody-009-Immunohistochemistry-Paraffin-NBP2-90081-img0003.jpg "Immunohistochemistry-Paraffin: HSF1 Antibody (009) [NBP2-90081] - Staining of human HSF1 in human tonsil with rabbit monoclonal antibody (1:200).")
![Immunohistochemistry-Paraffin: HSF1 Antibody (009) [NBP2-90081] - Staining of human HSF1 in human placenta with rabbit monoclonal antibody (1:200).](http://images.novusbio.com/fullsize/HSF1-Antibody-009-Immunohistochemistry-Paraffin-NBP2-90081-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: HSF1 Antibody (009) [NBP2-90081] - Staining of Human HSF1 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-90081 antibody (1:60) at 4? overnight. Then cells were stained with the Alexa Fluor 549-conjugated Goat Anti-rabbit IgG secondary antibody (red).](http://images.novusbio.com/fullsize/nbp2-90081_rabbit-monoclonal-hsf1-antibody-009-235202514492390.png)
![Immunohistochemistry-Paraffin: MANF Antibody [NBP2-99774] - Immunochemical staining of human MANF in human brain with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/MANF-Antibody-Immunohistochemistry-Paraffin-NBP2-99774-img0002.jpg "Immunohistochemistry-Paraffin: MANF Antibody [NBP2-99774] - Immunochemical staining of human MANF in human brain with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: MANF Antibody [NBP2-99774] - Immunochemical staining of human MANF in human brain with NBP2-99774 at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/nbp2-99774_rabbit-polyclonal-manf-antibody-2352025162817.png)
![Immunocytochemistry/Immunofluorescence: MANF Antibody [NBP2-99774] - Immunofluorescence staining of MANF in U2OS cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-99774 antibody (dilution ratio 1:500) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG Secondary antibody (green) and counterstained with DAPI (blue).Positive staining was localized to Cytoplasm.](http://images.novusbio.com/fullsize/nbp2-99774_rabbit-polyclonal-manf-antibody-2352025213516.png)
![Immunohistochemistry: KIF2C Antibody (PSH01-51) [NBP3-32575] - Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-KIF2C antibody (NBP3-32575) at 1/200 dilution.<br/><br/> The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32575) at 1/200 dilution for 1 hour 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/nbp3-32575_rabbit-kif2c-mab-psh01-51-29820241433361.jpg "Immunohistochemistry: KIF2C Antibody (PSH01-51) [NBP3-32575] - Immunohistochemical analysis of paraffin-embedded human testis tissue with Rabbit anti-KIF2C antibody (NBP3-32575) at 1/200 dilution.<br/><br/> The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32575) at 1/200 dilution for 1 hour 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.")
![Western blot analysis on different lysates with NBP3-32575 at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: HepG2 cell lysate Lane 3: K-562 cell lysate Lane 4: Jurkat cell lysate Lane 5: 293T cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 81 kDa Observed band size: 81 kDa Exposure time: 5 minutes; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. NBP3-32575 at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG [HRP] Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32575_-western-blot-639204595244011280.jpg)
![Western Blot: Menin Antibody (JE30-97) [NBP3-32588] - Western blot analysis of Menin on different lysates with Rabbit anti-Menin antibody (NBP3-32588) at 1/500 dilution.<br/><br/> Lane 1: 293 cell lysate<br/> Lane 2: PC-3M cell lysate<br/> Lane 3: Jurkat cell lysate<br/><br/> Lysates/proteins at 10 ug/Lane.<br/><br/> Predicted band size: 68 kDa<br/> Observed band size: 68 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 8% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32588) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32588_rabbit-menin-mab-je30-97-27820241631650.png "Western Blot: Menin Antibody (JE30-97) [NBP3-32588] - Western blot analysis of Menin on different lysates with Rabbit anti-Menin antibody (NBP3-32588) at 1/500 dilution.<br/><br/> Lane 1: 293 cell lysate<br/> Lane 2: PC-3M cell lysate<br/> Lane 3: Jurkat cell lysate<br/><br/> Lysates/proteins at 10 ug/Lane.<br/><br/> Predicted band size: 68 kDa<br/> Observed band size: 68 kDa<br/><br/> Exposure time: 2 minutes;<br/><br/> 8% SDS-PAGE gel.<br/><br/> Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32588) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: Menin Antibody (JE30-97) [NBP3-32588] - Immunohistochemical analysis of paraffin-embedded human lung cancer tissue with Rabbit anti-Menin antibody (NBP3-32588) at 1/200 dilution.<br/><br/> The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32588) at 1/200 dilution for 1 hour 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/nbp3-32588_rabbit-menin-mab-je30-97-298202413585580.jpg)
![Western blot analysis on different lysates with NBP3-32588 at 1/1,000 dilution. Lane 1: HeLa (Human cervical adenocarcinoma cell) cell lysate Lane 2: NIH/3T3 (Mouse fibroblast) cell lysate Lane 3: PC-12 (Rat pheochromocytoma cell (undifferentiated)) cell lysate Lane 4: Rat testis tissue lysate Lysates/proteins at 20 µg/Lane. Exposure time: 3 minutes Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: NBP3-32588, 1/1,000 in 5% NFDM/TBST, overnight at 4 ℃ Secondary antibody: Goat Anti-Rabbit IgG [HRP] Secondary Antibody, 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 68 kDa Observed band size: 68 kDa](http://images.novusbio.com/fullsize/nbp3-32588_-western-blot-639204594554558475.jpg)
![Western Blot: p53R2 Antibody [NBP3-00079] - Anti-p53R2 rabbit polyclonal antibody at 1:500 dilution. Lane A: 293T Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 41 kDa. Observed band size: 50 kDa (We are unsure as to the identity of these extra bands).](http://images.novusbio.com/fullsize/p53R2-Antibody-Western-Blot-NBP3-00079-img0002.jpg "Western Blot: p53R2 Antibody [NBP3-00079] - Anti-p53R2 rabbit polyclonal antibody at 1:500 dilution. Lane A: 293T Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 41 kDa. Observed band size: 50 kDa (We are unsure as to the identity of these extra bands).")
![Immunohistochemistry-Paraffin: p53R2 Antibody [NBP3-00079] - Immunochemical staining of human RRM2B in human prostatic carcinomal with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/p53R2-Antibody-Immunohistochemistry-Paraffin-NBP3-00079-img0003.jpg)
![Immunohistochemistry-Paraffin: p53R2 Antibody [NBP3-00079] - Immunochemical staining of human p53R2 in human tonsil with rabbit polyclonal antibody (1:1000, formalin-fixed paraffin embedded sections). The left panel: tissue incubated with primary antibody; The right panel: tissue incubated with the mixture of primary antibody and antigen (recombinant protein).](http://images.novusbio.com/fullsize/p53R2-Antibody-Immunohistochemistry-Paraffin-NBP3-00079-img0004.jpg)
![Immunohistochemistry-Paraffin: TTK Antibody [NBP2-98832] - Staining of human TTK in human lung cancer with rabbit polyclonal antibody (1:1000).](http://images.novusbio.com/fullsize/TTK-Antibody-Immunohistochemistry-Paraffin-NBP2-98832-img0002.jpg "Immunohistochemistry-Paraffin: TTK Antibody [NBP2-98832] - Staining of human TTK in human lung cancer with rabbit polyclonal antibody (1:1000).")
![Immunohistochemistry-Paraffin: TTK Antibody [NBP2-98832] - Staining of human RPS27 in human lung cancer with NBP2-98832 (1:1000).](http://images.novusbio.com/fullsize/nbp2-98832_rabbit-polyclonal-ttk-antibody-235202511444413.png)
![Immunocytochemistry/Immunofluorescence: TTK Antibody [NBP2-98832] - Immunofluorescence staining of TTK in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98832 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-98832_rabbit-polyclonal-ttk-antibody-23520252135167.png)
![Immunohistochemistry-Paraffin: UNG Antibody [NBP2-98838] - Immunochemical staining of human UNG in human testis with rabbit polyclonal antibody (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/UNG-Antibody-Immunohistochemistry-Paraffin-NBP2-98838-img0003.jpg "Immunohistochemistry-Paraffin: UNG Antibody [NBP2-98838] - Immunochemical staining of human UNG in human testis with rabbit polyclonal antibody (1:2000, formalin-fixed paraffin embedded sections).")
![Immunohistochemistry-Paraffin: UNG Antibody [NBP2-98838] - Immunochemical staining of human UNG in human stomach with rabbit polyclonal antibody (1:2000, formalin-fixed paraffin embedded sections).](http://images.novusbio.com/fullsize/UNG-Antibody-Immunohistochemistry-Paraffin-NBP2-98838-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: UNG Antibody [NBP2-98838] - Immunofluorescence staining of UNG in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98838 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG Secondary antibody (red) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-98838_rabbit-polyclonal-ung-antibody-235202516144337.png)
![Western Blot: p16INK4a/CDKN2A Antibody [NBP2-98881] - Anti-p16INK4a/CDKN2A rabbit polyclonal antibody at 1:500 dilution. Lane A: Hela Whole Cell Lysate. Lane B: 293T Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 17 kDa. Observed band size: 17 kDa](http://images.novusbio.com/fullsize/p16INK4a-CDKN2A-Antibody-Western-Blot-NBP2-98881-img0005.jpg "Western Blot: p16INK4a/CDKN2A Antibody [NBP2-98881] - Anti-p16INK4a/CDKN2A rabbit polyclonal antibody at 1:500 dilution. Lane A: Hela Whole Cell Lysate. Lane B: 293T Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 17 kDa. Observed band size: 17 kDa")
![Immunoprecipitation: p16INK4a/CDKN2A Antibody [NBP2-98881] - p16INK4a/CDKN2A was immunoprecipitated using: Lane A: 0.5 mg Hela Whole Cell Lysate. Lane B: 0.5 mg 293T Whole Cell Lysate 2 ul anti-p16INK4a/CDKN2A rabbit polyclonal antibody and 60 ug of Immunomagnetic beads Protein G. Primary antibody: Anti-p16INK4a/CDKN2A rabbit polyclonal antibody, at 1:200 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 17 kDa. Observed band size: 17 kDa](http://images.novusbio.com/fullsize/p16INK4a-CDKN2A-Antibody-Immunoprecipitation-NBP2-98881-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: p16INK4a/CDKN2A Antibody [NBP2-98881] - Immunofluorescence staining of p16INK4a/CDKN2A in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98881 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG secondary antibody (red). Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-98881_rabbit-polyclonal-p16ink4a-cdkn2a-antibody-235202512205526.png)
![Western Blot: GTF2H3 Antibody [NBP2-87539] - WB Suggested Anti-GTF2H3 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:2500. Positive Control: Jurkat cell lysateGTF2H3 is supported by BioGPS gene expression data to be expressed in Jurkat](http://images.novusbio.com/fullsize/GTF2H3-Antibody-Western-Blot-NBP2-87539-img0003.jpg "Western Blot: GTF2H3 Antibody [NBP2-87539] - WB Suggested Anti-GTF2H3 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:2500. Positive Control: Jurkat cell lysateGTF2H3 is supported by BioGPS gene expression data to be expressed in Jurkat")
![Immunohistochemistry: GTF2H3 Antibody [NBP2-87539] - HumanMuscle](http://images.novusbio.com/fullsize/GTF2H3-Antibody-Immunohistochemistry-NBP2-87539-img0002.jpg)
![Immunohistochemistry-Paraffin: GTF2H3 Antibody [NBP2-87539] - Rabbit Anti-GTF2H3 antibody. Paraffin Embedded Tissue: Human Heart. Cellular Data: cardiac cell. Antibody Concentration: 4.0-8.0 ug/ml. Magnification: 400X](http://images.novusbio.com/fullsize/GTF2H3-Antibody-Immunohistochemistry-Paraffin-NBP2-87539-img0001.jpg)
![Western Blot: ASF1a Antibody [NBP2-98775] - Anti-ASF1a rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 23 kDa. Observed band size: 23 kDa (We are unsure as to the identity of these extra bands).](http://images.novusbio.com/fullsize/ASF1a-Antibody-Western-Blot-NBP2-98775-img0003.jpg "Western Blot: ASF1a Antibody [NBP2-98775] - Anti-ASF1a rabbit polyclonal antibody at 1:500 dilution. Lane A: Jurkat Whole Cell Lysate. Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight 800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 23 kDa. Observed band size: 23 kDa (We are unsure as to the identity of these extra bands).")
![Immunoprecipitation: ASF1a Antibody [NBP2-98775] - ASF1a was immunoprecipitated using: Lane A: 0.5 mg Hela Whole Cell Lysate 2 ul anti-ASF1a rabbit polyclonal antibody and 15 ul of 50 % Protein G agarose. Primary antibody: Anti-ASF1a rabbit polyclonal antibody, at 1:100 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size: 23 kDa. Observed band size: 35 kDa](http://images.novusbio.com/fullsize/ASF1a-Antibody-Immunoprecipitation-NBP2-98775-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: ASF1a Antibody [NBP2-98775] - Immunofluorescence staining of ASF1a in HeLa cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98775 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)594-conjugated Goat Anti-rabbit IgG secondary antibody (red). Positive staining was localized to nucleus.](http://images.novusbio.com/fullsize/nbp2-98775_rabbit-polyclonal-asf1a-antibody-235202521525077.png)