| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89364-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-27126-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-08997-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12074-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-75189-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12080-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52662-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52668-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50284-0.025ml | |||
![Flow Cytometry: CD40 Ligand/TNFSF5 Antibody (MR-1) [NBP1-47234] - Surface staining of activated murine splenocytes (PHA + PMA + ionomycin for 6 hours) using anti-CD154 (MR-1) FITC.](http://images.novusbio.com/fullsize/CD40-Ligand-TNFSF5-Antibody-MR-1-Flow-Cytometry-NBP1-47234-img0001.jpg "Flow Cytometry: CD40 Ligand/TNFSF5 Antibody (MR-1) [NBP1-47234] - Surface staining of activated murine splenocytes (PHA + PMA + ionomycin for 6 hours) using anti-CD154 (MR-1) FITC.")
![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: 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)
![Western Blot: Fc gamma RIIB/CD32b Antibody (110) [NBP2-89364] - Lane A: Daudi Whole Cell Lysate Lane B: THP1 Whole Cell LysateLysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:34 kDa Observed band size:38 kDa](http://images.novusbio.com/fullsize/Fc-gamma-RIIB-CD32b-Antibody-110-Western-Blot-NBP2-89364-img0002.jpg "Western Blot: Fc gamma RIIB/CD32b Antibody (110) [NBP2-89364] - Lane A: Daudi Whole Cell Lysate Lane B: THP1 Whole Cell LysateLysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:34 kDa Observed band size:38 kDa")
![Immunohistochemistry-Paraffin: Fc gamma RIIB/CD32b Antibody (110) [NBP2-89364] - Staining of human lymphonode showing membrane staining of B cells and some other mononuclear cell (1:10000).](http://images.novusbio.com/fullsize/Fc-gamma-RIIB-CD32b-Antibody-110-Immunohistochemistry-Paraffin-NBP2-89364-img0001.jpg)
![Western Blot: BAFFR/TNFRSF13C Antibody (5A9B10) [NBP3-27126] - Analysis using BAFFR/TNFRSF13C mAb against HEK293 (1) and BAFFR/TNFRSF13C (AA: extra 1-78)-hIgGFc transfected HEK293 (2) cell lysate.](http://images.novusbio.com/fullsize/nbp3-27126_mouse-baffr-tnfrsf13c-mab-5a9b10-bsa-free-1042024917029.jpg%3Fv=1666702823 "Western Blot: BAFFR/TNFRSF13C Antibody (5A9B10) [NBP3-27126] - Analysis using BAFFR/TNFRSF13C mAb against HEK293 (1) and BAFFR/TNFRSF13C (AA: extra 1-78)-hIgGFc transfected HEK293 (2) cell lysate.")
![Western Blot: BAFFR/TNFRSF13C Antibody (5A9B10) [NBP3-27126] - Analysis using BAFFR/TNFRSF13C mAb against human BAFFR/TNFRSF13C (AA: extra 1-78) recombinant protein. (Expected MW is 34 kDa)](http://images.novusbio.com/fullsize/nbp3-27126_mouse-baffr-tnfrsf13c-mab-5a9b10-bsa-free-10420249181944.jpg%3Fv=1666702823)
![ELISA: BAFFR/TNFRSF13C Antibody (5A9B10) [NBP3-27126] - Black line: Control Antigen (100 ng); Purple line: Antigen (10 ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng)](http://images.novusbio.com/fullsize/nbp3-27126_mouse-baffr-tnfrsf13c-mab-5a9b10-bsa-free-1042024920234.jpg%3Fv=1666702823)
![Flow Cytometry: BAFFR/TNFRSF13C Antibody (5A9B10) [NBP3-27126] - Analysis of Raji cells using BAFFR/TNFRSF13C mouse mAb (green) and negative control (red).](http://images.novusbio.com/fullsize/nbp3-27126_mouse-baffr-tnfrsf13c-mab-5a9b10-bsa-free-10420249181918.jpg%3Fv=1666702823)
![Immunocytochemistry/Immunofluorescence: Fc gamma RII/CD32 Antibody (AT130-5) - Chimeric [NBP3-08997] - Immunofluorescence analysis of paraformaldehyde fixed mouse (Mus musculus) splenocytes on Shi-fix(TM) coverslips, permeabilized with 0.15% Triton stained with the chimeric rabbit version of AT130-5 (NBP3-08997) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (1 ug/ml), showing membrane staining in a subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-08997, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/Fc-gamma-RII-CD32-Antibody-AT130-5-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-08997-img0001.jpg "Immunocytochemistry/Immunofluorescence: Fc gamma RII/CD32 Antibody (AT130-5) - Chimeric [NBP3-08997] - Immunofluorescence analysis of paraformaldehyde fixed mouse (Mus musculus) splenocytes on Shi-fix(TM) coverslips, permeabilized with 0.15% Triton stained with the chimeric rabbit version of AT130-5 (NBP3-08997) at 10 ug/ml for 1h followed by Alexa Fluor(R) 488 secondary antibody (1 ug/ml), showing membrane staining in a subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-08997, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor(R) 488 secondary antibody.")
![Western Blot: CD37 Antibody (IPO-24 (ZC37-24)) - Chimeric [NBP3-12074] - Daudi cell lysate(A), human spleen(B), and tonsil(C) tissue lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of IPO-24 (ZC37-24) (NBP3-12074) at 2 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.](http://images.novusbio.com/fullsize/CD37-Antibody-IPO-24-ZC37-24-Chimeric-Western-Blot-NBP3-12074-img0001.jpg "Western Blot: CD37 Antibody (IPO-24 (ZC37-24)) - Chimeric [NBP3-12074] - Daudi cell lysate(A), human spleen(B), and tonsil(C) tissue lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of IPO-24 (ZC37-24) (NBP3-12074) at 2 ug/ml before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.")
![Immunocytochemistry/Immunofluorescence: CD37 Antibody (IPO-24 (ZC37-24)) - Chimeric [NBP3-12074] - Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of IPO-24 (ZC37-24) (NBP3-12074) 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 NBP3-12074, 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/CD37-Antibody-IPO-24-ZC37-24-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12074-img0002.jpg)
![Flow Cytometry: Siglec-2/CD22 Antibody (hL22 (Epratuzumab)) - Chimeric [NBP2-75189] - Flow-cytometry using anti-CD22 antibody Epratuzumab. Rhesus monkey lymphocytes were stained with an isotype control (NBP2-52636, panel A) or the rabbit-chimeric version of Epratuzumab (NBP2-75189, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Siglec-2-CD22-Antibody-hL22-Epratuzumab-Chimeric-Flow-Cytometry-NBP2-75189-img0003.jpg "Flow Cytometry: Siglec-2/CD22 Antibody (hL22 (Epratuzumab)) - Chimeric [NBP2-75189] - Flow-cytometry using anti-CD22 antibody Epratuzumab. Rhesus monkey lymphocytes were stained with an isotype control (NBP2-52636, panel A) or the rabbit-chimeric version of Epratuzumab (NBP2-75189, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.")
![Flow Cytometry: Siglec-2/CD22 Antibody (hL22 (Epratuzumab)) - Chimeric [NBP2-75189] - Flow-cytometry using anti-CD22 antibody Epratuzumab. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of Eptratuzumab (NBP2-75189, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Siglec-2-CD22-Antibody-hL22-Epratuzumab-Chimeric-Flow-Cytometry-NBP2-75189-img0001.jpg)
![Flow Cytometry: Siglec-2/CD22 Antibody (hL22 (Epratuzumab)) - Chimeric [NBP2-75189] - Flow-cytometry using anti-CD22 antibody Epratuzumab. Cynomolgus monkey lymphocytes were stained with an isotype control (NBP2-52636, panel A) or the rabbit-chimeric version of Epratuzumab (NBP2-75189, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/Siglec-2-CD22-Antibody-hL22-Epratuzumab-Chimeric-Flow-Cytometry-NBP2-75189-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CD81 Antibody (1.3.3.22) - Chimeric [NBP3-12080] - Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of 1.3.3.22 (NBP3-12080) 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 NBP3-12080, 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/CD81-Antibody-1-3-3-22-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12080-img0001.jpg "Immunocytochemistry/Immunofluorescence: CD81 Antibody (1.3.3.22) - Chimeric [NBP3-12080] - Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of 1.3.3.22 (NBP3-12080) 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 NBP3-12080, 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.")
![Flow Cytometry: CD81 Antibody (1.3.3.22) - Chimeric - Azide and BSA Free [NBP3-12080] - Paraformaldehyde fixed Daudi cells were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-12080 (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/nbp3-12080_rabbit-monoclonal-cd81-antibody-1-3-3-22-chimeric-74202522141241.png)
![Flow Cytometry: CD19 Antibody (HD37) - Chimeric [NBP2-52662] - Flow-cytometry using anti-CD19 antibody HD37. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HD37 (NBP2-52662, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/CD19-Antibody-HD37-Chimeric-Flow-Cytometry-NBP2-52662-img0001.jpg "Flow Cytometry: CD19 Antibody (HD37) - Chimeric [NBP2-52662] - Flow-cytometry using anti-CD19 antibody HD37. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HD37 (NBP2-52662, panel B) at a concentration of 1 ug/ml for 30 mins at RT. After washing, bound antibody was detected using a AF488 conjugated donkey anti-rabbit antibody and cells analysed on a FACSCanto flow-cytometer.")
![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.")
![Western Blot: CD40/TNFRSF5 Antibody (T8P2G4/A6) [NBP2-50284] - Analysis of CD40 in Jurkat cell lysates.](http://images.novusbio.com/fullsize/CD40-TNFRSF5-Antibody-T8P2G4-A6-Western-Blot-NBP2-50284-img0001.jpg "Western Blot: CD40/TNFRSF5 Antibody (T8P2G4/A6) [NBP2-50284] - Analysis of CD40 in Jurkat cell lysates.")
![Immunohistochemistry-Paraffin: CD40/TNFRSF5 Antibody (T8P2G4/A6) [NBP2-50284] - Analysis of CD40 in a hepatocellular carcinoma tissue cross section.](http://images.novusbio.com/fullsize/CD40-TNFRSF5-Antibody-T8P2G4-A6-Immunohistochemistry-Paraffin-NBP2-50284-img0002.jpg)
![Immunohistochemistry: CD40/TNFRSF5 Antibody (T8P2G4/A6) [NBP2-50284] - Analysis of CD40 in a cross section of human breast cancer tissue. Positive cytoplasmic staining is shown.](http://images.novusbio.com/fullsize/CD40-TNFRSF5-Antibody-T8P2G4-A6-Immunohistochemistry-NBP2-50284-img0003.jpg)