| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89658-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-81055-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90470-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-52647-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11435 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11588 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-24279 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-21022 | |||
![Western Blot: CD38 Antibody (003) [NBP2-89658] - Lane A: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary antibody goat anti-Rabbit IgG H&L (DyLight 800) at 1:10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:34 kDa Observed band size:50 kDa.](http://images.novusbio.com/fullsize/CD38-Antibody-003-Western-Blot-NBP2-89658-img0001.jpg "Western Blot: CD38 Antibody (003) [NBP2-89658] - Lane A: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary antibody goat anti-Rabbit IgG H&L (DyLight 800) at 1:10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:34 kDa Observed band size:50 kDa.")
![Immunoprecipitation: CD38 Antibody (003) [NBP2-89658] - Lane A:0.5 mg Jurkat Whole Cell Lysate 4 uL anti-CD38 rabbit monoclonal antibody and 60 ug of Immunomagnetic beads Protein A/G. Primary antibody: Anti-CD38 rabbit monoclonal antibody at 1:100 dilution. Secondary antibody: Goat Anti-Rabbit IgG (H+L)/HRP at 1:10000 dilution Developed using the ECL technique. Performed under reducing conditions. Predicted band size: 45 kDa Observed band size: 45 kDa.](http://images.novusbio.com/fullsize/CD38-Antibody-003-Immunoprecipitation-NBP2-89658-img0002.jpg)
![Immunocytochemistry/Immunofluorescence: CD38 Antibody (AT13/5) [NBP2-81055] - Immunofluorescence staining of fixed Daudi cells with anti-CD38 antibody AT13/5 [NBP2-81055]. Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of AT13/5 [NBP2-81055] at 10 ug/mL for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/mL), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81055, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.](http://images.novusbio.com/fullsize/CD38-Antibody-AT13-5-Immunocytochemistry-Immunofluorescence-NBP2-81055-img0002.jpg "Immunocytochemistry/Immunofluorescence: CD38 Antibody (AT13/5) [NBP2-81055] - Immunofluorescence staining of fixed Daudi cells with anti-CD38 antibody AT13/5 [NBP2-81055]. Immunofluorescence analysis of paraformaldehyde fixed Daudi cells on Shi-fix coverslips, permeabilized with 0.15% Triton and stained with the chimeric rabbit IgG version of AT13/5 [NBP2-81055] at 10 ug/mL for 1h followed by Alexa Fluor 488 secondary antibody (1 ug/mL), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP2-81055, DAPI, merged channels and an isotype control. The isotype control was stained with an anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.")
![Western Blot: CD38 Antibody (AT13/5) [NBP2-81055] - Western Blot using anti-CD38 antibody (AT13/5) [NBP2-81055]. Human spleen lysate samples (35 ug protein in RIPA buffer) were resolved on a 10% SDS PAGE gel and blots probed with the chimeric rabbit version of AT13/5 [NBP2-81055] at 1 ug/mL before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence. The expected running size for CD38 is 34.3 kDa, but this protein is glycosylated at several residues. NBP2-81055 successfully detected CD38 in human spleen lysate.](http://images.novusbio.com/fullsize/CD38-Antibody-AT13-5-Western-Blot-NBP2-81055-img0001.jpg)
![Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse kidney with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.](http://images.novusbio.com/fullsize/CD38-Antibody-32-Immunohistochemistry-Paraffin-NBP2-90470-img0002.jpg "Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse kidney with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.")
![Immunohistochemistry-Paraffin: CD38 Antibody (32) [NBP2-90470] - Staining of mouse CD38 in mouse heart with rabbit monoclonal antibody (1:500, formalin-fixed paraffin embedded sections). Positive staining was localized to endotheliocyte.](http://images.novusbio.com/fullsize/CD38-Antibody-32-Immunohistochemistry-Paraffin-NBP2-90470-img0001.jpg)
![Flow Cytometry: CD38 Antibody (HB7) - Chimeric [NBP2-52647] - CD38 Antibody (HB7) [NBP2-52647] - Flow Cytometry using anti-CD38 antibody HB7. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HB7 (NBP2-52647, 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/CD38-Antibody-HB7-Chimeric-Flow-Cytometry-NBP2-52647-img0001.jpg "Flow Cytometry: CD38 Antibody (HB7) - Chimeric [NBP2-52647] - CD38 Antibody (HB7) [NBP2-52647] - Flow Cytometry using anti-CD38 antibody HB7. Human lymphocytes were stained with an isotype control (panel A) or the rabbit-chimeric version of HB7 (NBP2-52647, 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.")
