| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-99765-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89286-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52668-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20159-0.025mg | |||
| Conjugate | Catalog # | Availability | Size | Price |
|---|---|---|---|---|
| CoraFluor 1 | NBP2-52704CL1 | |||
| Janelia Fluor 525 | NBP2-52704JF525 | |||
| Janelia Fluor 669 | NBP2-52704JF669 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52704-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81049-0.025mg | |||
![Western Blot: Chymase/CMA1/Mast Cell Chymase Antibody (2O4P8) [NBP3-15389] - Analysis of extracts of various cell lines, using Chymase/CMA1/Mast Cell Chymase (CMA1) Rabbit mAb (NBP3-15389) 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. Detection: ECL Basic Kit. Exposure time: 10s.](http://images.novusbio.com/fullsize/Chymase-CMA1-Mast-Cell-Chymase-Antibody-2O4P8-Western-Blot-NBP3-15389-img0002.jpg "Western Blot: Chymase/CMA1/Mast Cell Chymase Antibody (2O4P8) [NBP3-15389] - Analysis of extracts of various cell lines, using Chymase/CMA1/Mast Cell Chymase (CMA1) Rabbit mAb (NBP3-15389) 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. Detection: ECL Basic Kit. Exposure time: 10s.")
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (2O4P8) [NBP3-15389] - Human appendix using Chymase/CMA1/Mast Cell Chymase (CMA1) Rabbit mAb (NBP3-15389) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/Chymase-CMA1-Mast-Cell-Chymase-Antibody-2O4P8-Immunohistochemistry-Paraffin-NBP3-15389-img0001.jpg)
![Immunohistochemistry: Chymase/CMA1/Mast Cell Chymase Antibody (CC1) [NB100-693] - Staining of a human tonsil cross section](http://images.novusbio.com/fullsize/Chymase-CMA1-Mast-Cell-Chymase-Antibody-CC1-Immunohistochemistry-NB100-693-img0004.jpg "Immunohistochemistry: Chymase/CMA1/Mast Cell Chymase Antibody (CC1) [NB100-693] - Staining of a human tonsil cross section")
![Immunohistochemistry-Paraffin: Chymase/CMA1/Mast Cell Chymase Antibody (CC1) [NB100-693] - Formalin fixed paraffin embedded human tonsil stained with Mast Cell Chymase antibody.](http://images.novusbio.com/fullsize/Chymase-CMA1-Mast-Cell-Chymase-Antibody-CC1-Immunohistochemistry-Paraffin-NB100-693-img0002.jpg)
![Western Blot: CD35 Antibody (A4G1-R) [NBP3-32150] - Western blot analysis of CD35 on different lysates with Mouse anti-CD35 antibody (NBP3-32150) at 1/2,000 dilution. Lane 1: TF-1 cell lysate Lane 2: Human kidney tissue lysate Lane 3: K-562 cell lysate (negative) Lysates/proteins at 20 ug/Lane. Predicted band size: 224 kDa Observed band size: 280 kDa Exposure time: 3 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. The primary antibody (NBP3-32150) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32150_mouse-cd35-mab-a4g1-r-278202416285277.jpg "Western Blot: CD35 Antibody (A4G1-R) [NBP3-32150] - Western blot analysis of CD35 on different lysates with Mouse anti-CD35 antibody (NBP3-32150) at 1/2,000 dilution. Lane 1: TF-1 cell lysate Lane 2: Human kidney tissue lysate Lane 3: K-562 cell lysate (negative) Lysates/proteins at 20 ug/Lane. Predicted band size: 224 kDa Observed band size: 280 kDa Exposure time: 3 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. The primary antibody (NBP3-32150) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CD35 Antibody (A4G1-R) [NBP3-32150] - Immunofluorescence analysis of paraffin-embedded human tonsil tissue labeling CD35 with Mouse anti-CD35 antibody (NBP3-32150) at 1/200 dilution. 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32150, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32150_mouse-cd35-mab-a4g1-r-298202413585556.jpg)
![Immunohistochemistry: CD35 Antibody (A4G1-R) [NBP3-32150] - Immunohistochemical analysis of paraffin-embedded human hodgkin lymphoma tissue with Mouse anti-CD35 antibody (NBP3-32150) at 1/500 dilution. 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 (NBP3-32150) at 1/500 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/nbp3-32150_mouse-cd35-mab-a4g1-r-298202413585599.jpg)
![Western Blot: CD97 Antibody [NBP2-99765] - Anti-CD97 rabbit polyclonal antibody at 1:500 dilution. Lane A: HL-60 Membrane Lysate. Lane B: K562 Membrane 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: 92 kDa. Observed band size: 70 kDa](http://images.novusbio.com/fullsize/CD97-Antibody-Western-Blot-NBP2-99765-img0005.jpg "Western Blot: CD97 Antibody [NBP2-99765] - Anti-CD97 rabbit polyclonal antibody at 1:500 dilution. Lane A: HL-60 Membrane Lysate. Lane B: K562 Membrane 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: 92 kDa. Observed band size: 70 kDa")
![Immunocytochemistry/Immunofluorescence: CD97 Antibody [NBP2-99765] - Immunofluorescence staining of CD97 in HeLa cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with rabbit anti-human CD97 polyclonal 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 cell membrane.](http://images.novusbio.com/fullsize/CD97-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-99765-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CD97 Antibody [NBP2-99765] - Immunofluorescence staining of CD97 in HeLa cells. Cells were fixed with 4% PFA, blocked with 10% serum, and incubated with NBP2-99765 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 cell membrane.](http://images.novusbio.com/fullsize/nbp2-99765_rabbit-polyclonal-cd97-antibody-235202511545614.png)
![Immunocytochemistry/Immunofluorescence: pIgR Antibody (007) [NBP2-89286] - Staining of PIGR in HepG2 cells. Cells were fixed with 4% PFA,blocked with 10% serum, and incubated with rabbit anti-Y PIGR monoclonal antibody (dilution ratio 1:60) 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/pIgR-Antibody-007-Immunocytochemistry-Immunofluorescence-NBP2-89286-img0003.jpg "Immunocytochemistry/Immunofluorescence: pIgR Antibody (007) [NBP2-89286] - Staining of PIGR in HepG2 cells. Cells were fixed with 4% PFA,blocked with 10% serum, and incubated with rabbit anti-Y PIGR monoclonal antibody (dilution ratio 1:60) 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.")
![Immunohistochemistry-Paraffin: pIgR Antibody (007) [NBP2-89286] - Staining of human PIGR in human liver (cirrhosis) with rabbit monoclonal antibody (1:60). Positive staining was localized to hepatocyte.](http://images.novusbio.com/fullsize/pIgR-Antibody-007-Immunohistochemistry-Paraffin-NBP2-89286-img0002.jpg)
![Immunohistochemistry-Paraffin: pIgR Antibody (007) [NBP2-89286] - Staining of human PIGR in human breast carcinoma with rabbit monoclonal antibody (1:60).](http://images.novusbio.com/fullsize/pIgR-Antibody-007-Immunohistochemistry-Paraffin-NBP2-89286-img0001.jpg)
![Western Blot: CD35 Antibody (A4F3-R) [NBP3-32149] - Western blot analysis of CD35 on different lysates with Mouse anti-CD35 antibody (NBP3-32149) at 1/2,000 dilution. Lane 1: TF-1 cell lysate Lane 2: Human kidney tissue lysate Lane 3: K-562 cell lysate (negative) Lysates/proteins at 20 ug/Lane. Predicted band size: 224 kDa Observed band size: 280 kDa Exposure time: 1 minute 14 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32149) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32149_mouse-cd35-mab-a4f3-r-278202415242650.jpg "Western Blot: CD35 Antibody (A4F3-R) [NBP3-32149] - Western blot analysis of CD35 on different lysates with Mouse anti-CD35 antibody (NBP3-32149) at 1/2,000 dilution. Lane 1: TF-1 cell lysate Lane 2: Human kidney tissue lysate Lane 3: K-562 cell lysate (negative) Lysates/proteins at 20 ug/Lane. Predicted band size: 224 kDa Observed band size: 280 kDa Exposure time: 1 minute 14 seconds; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32149) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CD35 Antibody (A4F3-R) [NBP3-32149] - Immunohistochemical analysis of paraffin-embedded human Hodgkin lymphoma tissue with Mouse anti-CD35 antibody (NBP3-32149) at 1/1,000 dilution. 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 (NBP3-32149) at 1/1,000 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/nbp3-32149_mouse-cd35-mab-a4f3-r-29820241435270.jpg)
![Immunohistochemistry: CD35 Antibody (A4F3-R) [NBP3-32149] - Immunofluorescence analysis of paraffin-embedded human tonsil tissue labeling CD35 with Mouse anti-CD35 antibody (NBP3-32149) at 1/200 dilution. 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32149, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Mouse IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32149_mouse-cd35-mab-a4f3-r-29820241420950.jpg)
![Immunocytochemistry/Immunofluorescence: CD46 Antibody (M037) [NBP3-23191] - Immunocytochemical labeling of CD46 in aldehyde fixed human NCIH1915 lung carcinoma cells. The cells were labeled with mouse monoclonal anti-CD46 (NBP3-23191). The antibody was detected using goat anti-mouse Ig:DyLight(R) 594.](http://images.novusbio.com/fullsize/nbp3-23191_mouse-cd46-mab-m037-19920231759445.jpg "Immunocytochemistry/Immunofluorescence: CD46 Antibody (M037) [NBP3-23191] - Immunocytochemical labeling of CD46 in aldehyde fixed human NCIH1915 lung carcinoma cells. The cells were labeled with mouse monoclonal anti-CD46 (NBP3-23191). The antibody was detected using goat anti-mouse Ig:DyLight(R) 594.")
![Immunocytochemistry/Immunofluorescence: CD46 Antibody (M037) [NBP3-23191] - Immunocytochemical labeling of CD46 in aldehyde fixed human NCIH1915 lung carcinoma cells. The cells were labeled with mouse monoclonal anti-CD46 (NBP3-23191). The antibody was detected using goat anti-mouse Ig:DyLight(R) 594.](http://images.novusbio.com/fullsize/nbp3-23191_mouse-cd46-mab-m037-19920231240371.jpg)
![Western Blot: CD46 Antibody (M037) [NBP3-23191] - Western blot of native lysates from NCI-H2052 mesothelial cells (lane 1), SK-MES-1 squamous carcinoma (lane 2), MDA-MB-231 breast carcinoma (lane 3), MeWo melanoma (lane 4), A431 skin adenocarcinoma (lane 5), LNCaP prostate cancer cells (lane 6), and MCF7 breast cancer cells (lane 7). The blot was probed with mouse monoclonal anti-CD46 (NBP3-23191) at 1:1000.](http://images.novusbio.com/fullsize/nbp3-23191_mouse-cd46-mab-m037-19920231240375.jpg)
![Immunohistochemistry: CD35 Antibody (8C12) - Chimeric [NBP2-52668] - Immunohistochemical staining of rat stomach using anti-Complement receptor 1 antibody NBP2-52668. Formalin fixed rat stomach slices were were stained with NBP2-52668 at 3 ug/ml.](http://images.novusbio.com/fullsize/CD35-Antibody-8C12-Chimeric-Immunohistochemistry-NBP2-52668-img0001.jpg "Immunohistochemistry: CD35 Antibody (8C12) - Chimeric [NBP2-52668] - Immunohistochemical staining of rat stomach using anti-Complement receptor 1 antibody NBP2-52668. Formalin fixed rat stomach slices were were stained with NBP2-52668 at 3 ug/ml.")
![Flow Cytometry: Fc gamma RIIA/CD32a Antibody (IV.3) - Chimeric - Azide and BSA Free [NBP3-20159] - Paraformaldehyde fixed U937 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or the rabbit IgG version of IV.3 (NBP3-20159, 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(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-20159_rabbit-fc-gamma-riia-cd32a-mab-iv-3-chimeric-azide-bsa-free-2742023924258.png "Flow Cytometry: Fc gamma RIIA/CD32a Antibody (IV.3) - Chimeric - Azide and BSA Free [NBP3-20159] - Paraformaldehyde fixed U937 cells permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or the rabbit IgG version of IV.3 (NBP3-20159, 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(R) 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.")
![Immunocytochemistry/Immunofluorescence: Fc gamma RIIA/CD32a Antibody (IV.3) - Chimeric - Azide and BSA Free [NBP3-20159] - Immunofluorescence analysis of paraformaldehyde fixed U937 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of IV.3 (NBP3-20159) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-20159, DAPI, merged channels and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-20159_rabbit-fc-gamma-riia-cd32a-mab-iv-3-chimeric-azide-bsa-free-2742023924281.png)
![Immunohistochemistry: CD35 Antibody (8C12) [NBP2-81049] - Formalin fixed rat stomach slices were were stained with NBP2-81049 at 3 ug/ml.](http://images.novusbio.com/fullsize/CD35-Antibody-8C12-Immunohistochemistry-NBP2-81049-img0001.jpg "Immunohistochemistry: CD35 Antibody (8C12) [NBP2-81049] - Formalin fixed rat stomach slices were were stained with NBP2-81049 at 3 ug/ml.")
![Immunohistochemistry-Paraffin: ABO, Blood Group A Antigen Antibody (HE-193) - Azide and BSA Free [NBP2-47869] - Human Colon Carcinoma stained with Blood Group Antigen A Monoclonal Antibody (HE-193)](http://images.novusbio.com/fullsize/ABO-Blood-Group-A-Antigen-Antibody-HE-193-Azide-and-BSA-Free-Immunohistochemistry-Paraffin-NBP2-47869-img0001.jpg "Immunohistochemistry-Paraffin: ABO, Blood Group A Antigen Antibody (HE-193) - Azide and BSA Free [NBP2-47869] - Human Colon Carcinoma stained with Blood Group Antigen A Monoclonal Antibody (HE-193)")