| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-03432-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-37985-20ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99648-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54478-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21773-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-21784-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-22302-50ul | |||
![Western Blot: Bub1 Antibody [NBP3-03432] - Analysis of extracts from normal (control) and BUB1 knockout (KO) HeLa cells, using Bub1 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.](http://images.novusbio.com/fullsize/Bub1-Antibody-Western-Blot-NBP3-03432-img0001.jpg "<b>Genetic Strategies Validation. </b>Western Blot: Bub1 Antibody [NBP3-03432] - Analysis of extracts from normal (control) and BUB1 knockout (KO) HeLa cells, using Bub1 antibody at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.")
![Western Blot: PLK4 Antibody [NBP3-37985] - Western blot analysis of various lysates using PLK4 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 15s.](http://images.novusbio.com/fullsize/nbp3-37985_rabbit-plk4-pab-101220241134335.jpg "Western Blot: PLK4 Antibody [NBP3-37985] - Western blot analysis of various lysates using PLK4 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 15s.")
![Immunohistochemistry-Paraffin: PRC1 Antibody [NBP2-99648] - Immunochemical staining of human PRC1 in human brain with rabbit polyclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/PRC1-Antibody-Immunohistochemistry-Paraffin-NBP2-99648-img0002.jpg "Immunohistochemistry-Paraffin: PRC1 Antibody [NBP2-99648] - Immunochemical staining of human PRC1 in human brain with rabbit polyclonal antibody at 1:200 dilution, formalin-fixed paraffin embedded sections.")
![Immunocytochemistry/Immunofluorescence: PRC1 Antibody [NBP2-99648] - Immunofluorescence staining of PRC1 in U251MG cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-99648 antibody (dilution ratio 1:200) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus and Cytoplasm and cell membrane.](http://images.novusbio.com/fullsize/nbp2-99648_rabbit-polyclonal-prc1-antibody-23520251628112.png)
![Western Blot: BubR1 Antibody (7H4) [NBP3-15207] - Positive WB detected in: K562 whole cell lysate, U-251 whole cell lysate. All lanes: BubR1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 120, 106, 122 KDa. Observed band size: 125 KDa.](http://images.novusbio.com/fullsize/BubR1-Antibody-7H4-Western-Blot-NBP3-15207-img0002.jpg "Western Blot: BubR1 Antibody (7H4) [NBP3-15207] - Positive WB detected in: K562 whole cell lysate, U-251 whole cell lysate. All lanes: BubR1 antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 120, 106, 122 KDa. Observed band size: 125 KDa.")
![Flow Cytometry: BubR1 Antibody (7H4) [NBP3-15207] - Overlay histogram showing Hela cells stained with BubR1 antibody (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 followedby the antibody (1ug/1*106cells) 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*106cells) used under the same conditions. Acquisition of >10,000 events was performed.](http://images.novusbio.com/fullsize/BubR1-Antibody-7H4-Flow-Cytometry-NBP3-15207-img0001.jpg)
![Western Blot: Aurora B Antibody (AURKB/1521) [NBP2-53267] - Western Blot Analysis (A) Recombinant Protein (B) Human Liver Lysate Using Aurora B Monoclonal Antibody (AURKB/1521).](http://images.novusbio.com/fullsize/Aurora-B-Antibody-AURKB-1521-Western-Blot-NBP2-53267-img0001.jpg "Western Blot: Aurora B Antibody (AURKB/1521) [NBP2-53267] - Western Blot Analysis (A) Recombinant Protein (B) Human Liver Lysate Using Aurora B Monoclonal Antibody (AURKB/1521).")
![Western Blot: NDC80 Antibody (SR2187) [NBP3-21773] - Western blot analysis using NBP3-21773 in Jurkat cell lysate.](http://images.novusbio.com/fullsize/nbp3-21773_rabbit-ndc80-mab-sr2187-57202315521811.jpg "Western Blot: NDC80 Antibody (SR2187) [NBP3-21773] - Western blot analysis using NBP3-21773 in Jurkat cell lysate.")
![Western Blot: RASSF1 Antibody (SR1658) [NBP3-21784] - Western blot analysis using NBP3-21784 in HeLa cell lysate.](http://images.novusbio.com/fullsize/nbp3-21784_rabbit-rassf1-mab-sr1658-5720231558485.jpg "Western Blot: RASSF1 Antibody (SR1658) [NBP3-21784] - Western blot analysis using NBP3-21784 in HeLa cell lysate.")
![Western Blot: FKBP38 Antibody (SR1916) [NBP3-22302] - Western blot analysis using NBP3-22302 in Jurkat cell lysate.](http://images.novusbio.com/fullsize/nbp3-22302_rabbit-fkbp38-mab-sr1916-57202315521831.jpg "Western Blot: FKBP38 Antibody (SR1916) [NBP3-22302] - Western blot analysis using NBP3-22302 in Jurkat cell lysate.")
![Western Blot: NUP98 Antibody (S01-6F4) [NBP3-15070] - Western blot detection of NUP98 in Hela, A549, HL-60 cell lysates using NUP98 Rabbit mAb (1:1000 diluted). Predicted band size: 198kDa. Observed band size: 98kDa.](http://images.novusbio.com/fullsize/NUP98-Antibody-S01-6F4-Western-Blot-NBP3-15070-img0001.jpg "Western Blot: NUP98 Antibody (S01-6F4) [NBP3-15070] - Western blot detection of NUP98 in Hela, A549, HL-60 cell lysates using NUP98 Rabbit mAb (1:1000 diluted). Predicted band size: 198kDa. Observed band size: 98kDa.")
![Western Blot: TPX2 Antibody (S05-1B5) [NBP3-19921] - Western blot detection of TPX2 in Hela, A549, HL-60 cell lysates using NBP3-19921 (1:1000 diluted). Predicted band size: 86kDa. Observed band size: 100kDa.](http://images.novusbio.com/fullsize/TPX2-Antibody-S05-1B5-Western-Blot-NBP3-19921-img0001.jpg "Western Blot: TPX2 Antibody (S05-1B5) [NBP3-19921] - Western blot detection of TPX2 in Hela, A549, HL-60 cell lysates using NBP3-19921 (1:1000 diluted). Predicted band size: 86kDa. Observed band size: 100kDa.")
![Western Blot: PLK1 [p Thr210] Antibody [NB100-61108] - Rat synaptic membrane showing specific immunolabeling of the ~66 k PLK protein phosphorylated at Thr210 (control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambda-Ptase). The blot is identical to the control except that it was incubated in lambda-Ptase (1200 units for 30 min) before being exposed to the phospho-Thr210 PLK antibody. The immunolabeling is completely eliminated by treatment with lambda-Ptase.](http://images.novusbio.com/fullsize/PLK1-[p-Thr210]-Antibody-Western-Blot-NB100-61108-img0001.jpg "Western Blot: PLK1 [p Thr210] Antibody [NB100-61108] - Rat synaptic membrane showing specific immunolabeling of the ~66 k PLK protein phosphorylated at Thr210 (control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambda-Ptase). The blot is identical to the control except that it was incubated in lambda-Ptase (1200 units for 30 min) before being exposed to the phospho-Thr210 PLK antibody. The immunolabeling is completely eliminated by treatment with lambda-Ptase.")
![Flow Cytometry: UbcH10/UBE2C Antibody (SAIC-41C-6) - BSA Free [NBP3-43536] - Paraformaldehyde fixed MCF7 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43536 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-43536_rabbit-ubch10-ube2c-mab-saic-41c-6-azide-and-bsa-free-74202522113047.png "Flow Cytometry: UbcH10/UBE2C Antibody (SAIC-41C-6) - BSA Free [NBP3-43536] - Paraformaldehyde fixed MCF7 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-43536 (blue line) at a dilution of 1:100 for 1h at RT. After washing, the bound antibody was detected using a goat anti-rabbit IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.")
![Immunocytochemistry /Immunofluorescence: UbcH10/UBE2C Antibody (SAIC-41C-6) - BSA Free [NBP3-43536] - Immunofluorescence analysis of paraformaldehyde fixed Caco-2 cells permeabilized with 0.15% Triton stained with NBP3-43536 (1:100 dilution) for 1h followed by Alexa Fluor 488 secondary antibody (1:1000 dilution), showing nuclear staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-43536, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43536_rabbit-ubch10-ube2c-mab-saic-41c-6-azide-and-bsa-free-74202522141217.png)