| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47822-0.1mg | |||
| IHC-Prediluted | NBP2-48467 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-47811-0.1mg | |||
| IHC-Prediluted | NBP2-48037 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26404-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26526-50ul | |||
![Immunohistochemistry-Paraffin: CD59 Antibody (MACIF/1193) [NBP2-44702] - Human Tongue stained with CD59 Monoclonal Antibody (MACIF/1193)](http://images.novusbio.com/fullsize/CD59-Antibody-MACIF-1193-Immunohistochemistry-Paraffin-NBP2-44702-img0001.jpg "Immunohistochemistry-Paraffin: CD59 Antibody (MACIF/1193) [NBP2-44702] - Human Tongue stained with CD59 Monoclonal Antibody (MACIF/1193)")
![Immunohistochemistry-Paraffin: Cdc20 Antibody (CDC20/1102) [NBP2-44407] - Human Tonsil stained with CDC20 Monoclonal Antibody (CDC20/1102)](http://images.novusbio.com/fullsize/Cdc20-Antibody-CDC20-1102-Immunohistochemistry-Paraffin-NBP2-44407-img0002.jpg "Immunohistochemistry-Paraffin: Cdc20 Antibody (CDC20/1102) [NBP2-44407] - Human Tonsil stained with CDC20 Monoclonal Antibody (CDC20/1102)")
![Immunohistochemistry-Paraffin: Cdc20 Antibody (CDC20/1102) [NBP2-44407] - Human Gastric Carcinoma stained with CDC20 Monoclonal Antibody (CDC20/1102)](http://images.novusbio.com/fullsize/Cdc20-Antibody-CDC20-1102-Immunohistochemistry-Paraffin-NBP2-44407-img0001.jpg)
![Western Blot: c-Myc [p Ser62] Antibody (2A10) [NBP3-26404] - Positive Western Blot detected in Hela whole cell lysate. All lanes: c-Myc [p Ser62] Antibody at 1.4ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 57 KDa Observed band size: 57 KDa](http://images.novusbio.com/fullsize/nbp3-26404_rabbit-c-myc-p-ser-62-mab-2a10-282202411363014.jpg "Western Blot: c-Myc [p Ser62] Antibody (2A10) [NBP3-26404] - Positive Western Blot detected in Hela whole cell lysate. All lanes: c-Myc [p Ser62] Antibody at 1.4ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 57 KDa Observed band size: 57 KDa")
![Immunocytochemistry/Immunofluorescence: c-Myc [p Ser62] Antibody (2A10) [NBP3-26404] - Staining of Hela cells with c-Myc [p Ser62] Antibody (2A10) 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/nbp3-26404_rabbit-c-myc-p-ser-62-mab-2a10-282202412475135.jpg)
![Western Blot: MRPL15 Antibody [NBP2-19399] - HeLa whole cell and membrane extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with MRPL15 antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/MRPL15-Antibody-Western-Blot-NBP2-19399-img0004.jpg "Western Blot: MRPL15 Antibody [NBP2-19399] - HeLa whole cell and membrane extracts (30 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with MRPL15 antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")
![Western Blot: MRPL15 Antibody [NBP2-19399] - Various tissue extracts (50 ug) were separated by 12% SDS-PAGE, and the membrane was blotted with MRPL15 antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/MRPL15-Antibody-Western-Blot-NBP2-19399-img0002.jpg)
![Western Blot: eIF4A1 Antibody (7C3) [NBP3-15220] - Positive WB detected in: K562 whole cell lysate, 293 whole cell lysate, RAW264.7 whole cell lysate. All lanes: eIF4A1 Antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 40, 47 KDa. Observed band size: 50 KDa.](http://images.novusbio.com/fullsize/eIF4A1-Antibody-7C3-Western-Blot-NBP3-15220-img0002.jpg "Western Blot: eIF4A1 Antibody (7C3) [NBP3-15220] - Positive WB detected in: K562 whole cell lysate, 293 whole cell lysate, RAW264.7 whole cell lysate. All lanes: eIF4A1 Antibody at 1:1000. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 40, 47 KDa. Observed band size: 50 KDa.")
![Immunocytochemistry/Immunofluorescence: eIF4A1 Antibody (7C3) [NBP3-15220] - Immunofluorescence staining of Hela Cells with at eIF4A1 antibody 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-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/eIF4A1-Antibody-7C3-Immunocytochemistry-Immunofluorescence-NBP3-15220-img0001.jpg)
![Immunoprecipitation: CRM1 Antibody [NB100-79811] - Detection of CRM1 (Exportin 1) by Immunoprecipitation. Samples: Whole cell lysate (1 mg/IP; 1/4 of reaction loaded/lane) from HeLa cells. Antibodies: Affinity purified rabbit anti-CRM1 antibody BL1956 (Cat. No. NB100-79811) used at 3 mcg/mg lysate for IP.](http://images.novusbio.com/fullsize/CRM1-Antibody-Immunoprecipitation-NB100-79811-img0002.jpg "Immunoprecipitation: CRM1 Antibody [NB100-79811] - Detection of CRM1 (Exportin 1) by Immunoprecipitation. Samples: Whole cell lysate (1 mg/IP; 1/4 of reaction loaded/lane) from HeLa cells. Antibodies: Affinity purified rabbit anti-CRM1 antibody BL1956 (Cat. No. NB100-79811) used at 3 mcg/mg lysate for IP.")
![Western Blot: CKAP2 Antibody [NBP1-21391] - Detection of human CKAP2 by western blot. Samples:Whole cell lysate (15 ug) from HeLa, HEK293T, and Jurkat cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-CKAP2 antibody NBP1-21391 used for WB at 0.1 ug/ml. Detection:Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/CKAP2-Antibody-Western-Blot-NBP1-21391-img0003.jpg "Western Blot: CKAP2 Antibody [NBP1-21391] - Detection of human CKAP2 by western blot. Samples:Whole cell lysate (15 ug) from HeLa, HEK293T, and Jurkat cells prepared using NETN lysis buffer. Antibody: Affinity purified rabbit anti-CKAP2 antibody NBP1-21391 used for WB at 0.1 ug/ml. Detection:Chemiluminescence with an exposure time of 30 seconds.")
![<b>Independent Antibodies Validation. </b>Immunoprecipitation: CKAP2 Antibody [NBP1-21391] - Detection of human CKAP2 by western blot of immunoprecipitates. Samples: Whole cell lysate (1.0 mg per IP reaction; 20% of IP loaded) from HeLa, cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-CKAP2 antibody NBP1-21391 used for IP at 3 ug per reaction. CKAP2 was also immunoprecipitated by rabbit anti-CKAP2 antibody NBP1-21390. For blotting immunoprecipitated CKAP2, NBP1-21391 was used at 0.4 ug/ml. Detection: Chemiluminescence with an exposure time of 30 seconds.](http://images.novusbio.com/fullsize/CKAP2-Antibody-Immunoprecipitation-NBP1-21391-img0004.jpg)
![Immunohistochemistry: Actin Antibody (4C1) [NBP3-26526] - Image of Actin Antibody diluted at 1:50 and staining in paraffin-embedded human skeletal muscle 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.72% DAB.](http://images.novusbio.com/fullsize/nbp3-26526_rabbit-actin-mab-4c1-262202415475615.jpg "Immunohistochemistry: Actin Antibody (4C1) [NBP3-26526] - Image of Actin Antibody diluted at 1:50 and staining in paraffin-embedded human skeletal muscle 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 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.72% DAB.")
![Immunohistochemistry: Actin Antibody (4C1) [NBP3-26526] - Image of Actin Antibody diluted at 1:50 and staining in paraffin-embedded human skeletal muscle 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 polymer IgG labeled by HRP and visualized using 0.72% DAB.](http://images.novusbio.com/fullsize/nbp3-26526_rabbit-actin-mab-4c1-26220241525331.jpg)
![Flow Cytometry: Actin Antibody (4C1) [NBP3-26526] - Overlay Peak curve showing A549 cells stained with Actin Antibody (4C1) (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/nbp3-26526_rabbit-actin-mab-4c1-282202414312747.jpg)
![Wild-type (WT) and MAT2B knockout (KO) 293T cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT2B antibody [N3C3] (NBP2-17230) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/nbp2-17230_rabbit-polyclonal-mat2b-antibody-western-blot-26112025194822.jpg "<b>Genetic Strategies Validation. </b>Wild-type (WT) and MAT2B knockout (KO) 293T cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with MAT2B antibody [N3C3] (NBP2-17230) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")