| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-29818-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26301-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26396-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26487-50ul | |||
![Western Blot: PPP2R4 Antibody (H5D12) [NBP2-29818] - This lot detected PP2A, B subunit, B56 delta in HeLa nuclear cell extract when it was tested at 1:2000 in blocking buffer.](http://images.novusbio.com/fullsize/PPP2R4-Antibody-H5D12-Western-Blot-NBP2-29818-img0001.jpg "Western Blot: PPP2R4 Antibody (H5D12) [NBP2-29818] - This lot detected PP2A, B subunit, B56 delta in HeLa nuclear cell extract when it was tested at 1:2000 in blocking buffer.")
![Western Blot: MAPRE1 Antibody (C7) [NBP3-41846] - Sample: Lane1: Hela cell lysate; Lane2: Jurkat cell lysate; Lane3: A431 cell lysate Primary Ab: 3ug/ml NBP3-41846; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41846_mouse-mapre1-mab-c7-612202421175923.jpg "Western Blot: MAPRE1 Antibody (C7) [NBP3-41846] - Sample: Lane1: Hela cell lysate; Lane2: Jurkat cell lysate; Lane3: A431 cell lysate Primary Ab: 3ug/ml NBP3-41846; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: MAPRE1 Antibody (C8) [NBP3-41844] - Sample: Lane1: Hela cell lysate; Lane2: Jurkat cell lysate; Lane3: A431 cell lysate Primary Ab: 3ug/ml NBP3-41844; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41844_mouse-mapre1-mab-c8-612202421262958.jpg "Western Blot: MAPRE1 Antibody (C8) [NBP3-41844] - Sample: Lane1: Hela cell lysate; Lane2: Jurkat cell lysate; Lane3: A431 cell lysate Primary Ab: 3ug/ml NBP3-41844; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![ELISA: Somatostatin R2/SSTR2 Antibody (7A9) [NBP3-26301] - The Binding Activity of Human Somatostatin R2/SSTR2 with Somatostatin R2/SSTR2 Antibody.Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Somatostatin R2/SSTR2 at 10 ug/mL can bind Somatostatin R2/SSTR2 Antibody, the EC50 is 58.13-81.28 ng/mL.](http://images.novusbio.com/fullsize/nbp3-26301_human-somatostatin-r2-sstr2-mab-7a9-26220241227232.jpg "ELISA: Somatostatin R2/SSTR2 Antibody (7A9) [NBP3-26301] - The Binding Activity of Human Somatostatin R2/SSTR2 with Somatostatin R2/SSTR2 Antibody.Activity: Measured by its binding ability in a functional ELISA. Immobilized Human Somatostatin R2/SSTR2 at 10 ug/mL can bind Somatostatin R2/SSTR2 Antibody, the EC50 is 58.13-81.28 ng/mL.")
![Flow Cytometry: Somatostatin R2/SSTR2 Antibody (7A9) [NBP3-26301] - Untransfected CT26 cells (green line) and transfected Human SSTR2 CT26 stable cells (red line) were stained with anti-SSTR2 recombinant antibody (2ug/1*10^6 cells), washed and then followed by APC-conjugated anti-Human IgG Fc antibody and analyzed with flow cytometry.](http://images.novusbio.com/fullsize/nbp3-26301_human-somatostatin-r2-sstr2-mab-7a9-282202414312763.jpg)
![Immunocytochemistry/Immunofluorescence: RPA2 [p Thr21] Antibody (3B2) [NBP3-26396] - Staining of Hela cells with RPA2 [p Thr21] Antibody (3B2) 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/nbp3-26396_rabbit-rpa2-p-thr-21-mab-3b2-282202412493635.jpg "Immunocytochemistry/Immunofluorescence: RPA2 [p Thr21] Antibody (3B2) [NBP3-26396] - Staining of Hela cells with RPA2 [p Thr21] Antibody (3B2) 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).")
![Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1H8) [NBP3-26487] - Staining of Hela Cells with Aurora A Antibody (1H8) 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/nbp3-26487_rabbit-aurora-a-mab-1h8-282202412493636.jpg "Immunocytochemistry/Immunofluorescence: Aurora A Antibody (1H8) [NBP3-26487] - Staining of Hela Cells with Aurora A Antibody (1H8) 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).")
![Immunohistochemistry: Somatostatin R2/SSTR2 Antibody (1C3) [NBP3-15215] - IHC image of Somatostatin R2/SSTR2 antibody diluted at 1:100 and staining in paraffin-embedded human pancreatic tissue. 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 30 minutes 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/Somatostatin-R2-SSTR2-Antibody-1C3-Immunohistochemistry-NBP3-15215-img0001.jpg "Immunohistochemistry: Somatostatin R2/SSTR2 Antibody (1C3) [NBP3-15215] - IHC image of Somatostatin R2/SSTR2 antibody diluted at 1:100 and staining in paraffin-embedded human pancreatic tissue. 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 30 minutes 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.")