| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-13777-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54450-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26459-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-54317-100ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26697-50ul | |||
![Immunohistochemistry-Paraffin: Plasmolipin Antibody [NBP2-13777] - Staining in human cerebral cortex and lymph node tissues using anti-PLLP antibody. Corresponding PLLP RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/Plasmolipin-Antibody-Immunohistochemistry-Paraffin-NBP2-13777-img0005.jpg "<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: Plasmolipin Antibody [NBP2-13777] - Staining in human cerebral cortex and lymph node tissues using anti-PLLP antibody. Corresponding PLLP RNA-seq data are presented for the same tissues.")
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: Plasmolipin Antibody [NBP2-13777] - Staining of human lymph node shows low expression as expected.](http://images.novusbio.com/fullsize/Plasmolipin-Antibody-Immunohistochemistry-Paraffin-NBP2-13777-img0004.jpg)
![Immunohistochemistry-Paraffin: Plasmolipin Antibody [NBP2-13777] - Staining of human cerebral cortex shows high expression.](http://images.novusbio.com/fullsize/Plasmolipin-Antibody-Immunohistochemistry-Paraffin-NBP2-13777-img0003.jpg)
![Western Blot: Slit2 Antibody [NB600-881] - Analysis of a band at 165 kDa (lane 1) corresponding to SLIT-2 present in a chicken spinal cord whole cell lysate (arrowhead). Approximately 30 ug of lysate was separated on a 4-20% Tris-Glycine gel by SDS-PAGE and transferred onto nitrocellulose. After blocking the membrane was probed with the primary antibody diluted to 1:1,350. Reaction occurred overnight at 4 C followed by washes and reaction with a 1:10,000 dilution of IRDye800 conjugated Gt-a-Rabbit IgG [H&L] MX for 45 min at room temperature (800 nm channel, green).](http://images.novusbio.com/fullsize/Slit2-Antibody-Western-Blot-NB600-881-img0009.jpg "Western Blot: Slit2 Antibody [NB600-881] - Analysis of a band at 165 kDa (lane 1) corresponding to SLIT-2 present in a chicken spinal cord whole cell lysate (arrowhead). Approximately 30 ug of lysate was separated on a 4-20% Tris-Glycine gel by SDS-PAGE and transferred onto nitrocellulose. After blocking the membrane was probed with the primary antibody diluted to 1:1,350. Reaction occurred overnight at 4 C followed by washes and reaction with a 1:10,000 dilution of IRDye800 conjugated Gt-a-Rabbit IgG [H&L] MX for 45 min at room temperature (800 nm channel, green).")
![Immunohistochemistry: Slit2 Antibody [NB600-881] - Analysis of human breast carcinoma Tissue: Human prostate Fixation: FFPE buffered formalin 10% conc Ag Retrieval: Heat, Citrate pH 6.2. Pressure Cooker, EDTA pH 9.5 Pressure Cooker Primary antibody: 2ug/ml 1.5 hour @ room T Secondary Ab: MACH 1 HRP POLYMER 1:50 45” RT](http://images.novusbio.com/fullsize/Slit2-Antibody-Immunohistochemistry-NB600-881-img0005.jpg)
![Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Uterus stained with ASRGL1 Monoclonal Antibody (CRASH/1289).](http://images.novusbio.com/fullsize/ASRGL1-Antibody-CRASH-1289-Immunohistochemistry-Paraffin-NBP2-47648-img0003.jpg "Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Uterus stained with ASRGL1 Monoclonal Antibody (CRASH/1289).")
![Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Fallopian Tube stained with ASRGL1 Monoclonal Antibody (CRASH/1289).](http://images.novusbio.com/fullsize/ASRGL1-Antibody-CRASH-1289-Immunohistochemistry-Paraffin-NBP2-47648-img0001.jpg)
![Immunohistochemistry-Paraffin: ASRGL1 Antibody (CRASH/1289) [NBP2-47648] - Formalin-fixed, paraffin-embedded human Endometrium stained with ASRGL1 Monoclonal Antibody (CRASH/1289).](http://images.novusbio.com/fullsize/ASRGL1-Antibody-CRASH-1289-Immunohistochemistry-Paraffin-NBP2-47648-img0002.jpg)
![Western Blot: NPRB/NPR2 Antibody (19C7) [NBP3-26459] - Positive Western Blot detected in: HEPG2 whole cell lysate, MCF7 whole cell lysate. All lanes: NPRB/NPR2 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 117 kDa Observed band size: 117 kDa](http://images.novusbio.com/fullsize/nbp3-26459_rabbit-nprb-npr2-mab-19c7-28220241141361.jpg "Western Blot: NPRB/NPR2 Antibody (19C7) [NBP3-26459] - Positive Western Blot detected in: HEPG2 whole cell lysate, MCF7 whole cell lysate. All lanes: NPRB/NPR2 Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 117 kDa Observed band size: 117 kDa")
![Immunocytochemistry/Immunofluorescence: NPRB/NPR2 Antibody (19C7) [NBP3-26459] - Staining of Hela with NPRB/NPR2 Antibody (19C7) at 1:25, 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 501-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26459_rabbit-nprb-npr2-mab-19c7-28220241323613.jpg)
![Flow Cytometry: NPRB/NPR2 Antibody (19C7) [NBP3-26459] - Overlay Peak curve showing Hela cells stained with NPRB/NPR2 Antibody (19C7) (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/nbp3-26459_rabbit-nprb-npr2-mab-19c7-282202414183651.jpg)
![Immunohistochemistry-Paraffin: TSHR Antibody (SPM222) [NBP2-53224] - Formalin-fixed, paraffin-embedded human Thyroid Carcinoma stained with TSHRB Monoclonal Antibody (SPM222).](http://images.novusbio.com/fullsize/TSHR-Antibody-SPM222-Immunohistochemistry-Paraffin-NBP2-53224-img0001.jpg "Immunohistochemistry-Paraffin: TSHR Antibody (SPM222) [NBP2-53224] - Formalin-fixed, paraffin-embedded human Thyroid Carcinoma stained with TSHRB Monoclonal Antibody (SPM222).")
![Western Blot: Caspase-9 Antibody (2D5) [NBP3-26697] - Positive Western Blot detected in: HL-60 whole cell lysate, LO2 whole cell lysate. All lanes: Caspase-9 Antibody at 1.8ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 47, 31, 18, 37 KDa Observed band size: 47 KDa](http://images.novusbio.com/fullsize/nbp3-26697_rabbit-caspase-9-mab-2d5-28220241140940.jpg "Western Blot: Caspase-9 Antibody (2D5) [NBP3-26697] - Positive Western Blot detected in: HL-60 whole cell lysate, LO2 whole cell lysate. All lanes: Caspase-9 Antibody at 1.8ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 47, 31, 18, 37 KDa Observed band size: 47 KDa")
![Immunocytochemistry/Immunofluorescence: Caspase-9 Antibody (2D5) [NBP3-26697] - Staining of HepG2 cells with Caspase-9 Antibody (2D5) at 1:60, 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/nbp3-26697_rabbit-caspase-9-mab-2d5-28220241323614.jpg)
![Flow Cytometry: Caspase-9 Antibody (2D5) [NBP3-26697] - Overlay histogram showing K562 cells stained with Caspase-9 Antibody (2D5) (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/nbp3-26697_rabbit-caspase-9-mab-2d5-282202414183649.jpg)