| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-75904SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-50434-0.025ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11982-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-11995-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12000-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35227-10ug | |||
| Carrier-Free | NBP2-35227-1mg | |||
| Carrier-Free | NBP2-35227-500ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-20156-0.025mg | |||
![Flow Cytometry: Rat Monoclonal Integrin alpha 5/CD49e Antibody (5H10-27 (MFR5)) [NBP3-09130] - Separation of murine bone marrow cells stained using anti-mouse CD49e (5H10-27(MFR5)) purified antibody (concentration in sample 0.56 ug/ml, DAR APC) from murine bone marrow cells unstained by primary antibody (DAR APC, black-dashed) in flow cytometry analysis (surface staining).](http://images.novusbio.com/fullsize/antibody/nbp3-09130_rat-monoclonal-integrin-alpha-5-cd49e-antibody-5h10-27-mfr5-flow-cytometry-12122024143343..jpg "Flow Cytometry: Rat Monoclonal Integrin alpha 5/CD49e Antibody (5H10-27 (MFR5)) [NBP3-09130] - Separation of murine bone marrow cells stained using anti-mouse CD49e (5H10-27(MFR5)) purified antibody (concentration in sample 0.56 ug/ml, DAR APC) from murine bone marrow cells unstained by primary antibody (DAR APC, black-dashed) in flow cytometry analysis (surface staining).")
![Western Blot: CD11b Antibody (PSH03-96) [NBP3-32121] - Western blot analysis of CD11b on different lysates with Rabbit anti-CD11b antibody (NBP3-32121) at 1/2,000 dilution. Lane 1: TF-1 cell lysate (10 ug/Lane) Lane 2: THP-1 cell lysate (15 ug/Lane) Lane 3: U-937 cell lysate (30 ug/Lane) Lane 4: Jurkat cell lysate (negative) (10 ug/Lane) Lane 5: RAW264.7 cell lysate (5 ug/Lane) Lane 6: J774A.1 cell lysate (5 ug/Lane) Predicted band size: 127 kDa Observed band size: 170 kDa Exposure time: 59 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 (NBP3-32121) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32121_rabbit-cd11b-mab-psh03-96-278202415295518.jpg "Western Blot: CD11b Antibody (PSH03-96) [NBP3-32121] - Western blot analysis of CD11b on different lysates with Rabbit anti-CD11b antibody (NBP3-32121) at 1/2,000 dilution. Lane 1: TF-1 cell lysate (10 ug/Lane) Lane 2: THP-1 cell lysate (15 ug/Lane) Lane 3: U-937 cell lysate (30 ug/Lane) Lane 4: Jurkat cell lysate (negative) (10 ug/Lane) Lane 5: RAW264.7 cell lysate (5 ug/Lane) Lane 6: J774A.1 cell lysate (5 ug/Lane) Predicted band size: 127 kDa Observed band size: 170 kDa Exposure time: 59 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 (NBP3-32121) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: CD11b Antibody (PSH03-96) [NBP3-32121] - Immunohistochemical analysis of paraffin-embedded human cervical cancer tissue with Rabbit anti-CD11b antibody (NBP3-32121) at 1/5,000 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 (NBP3-32121) at 1/5,000 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/nbp3-32121_rabbit-cd11b-mab-psh03-96-29820241435252.jpg)
![Immunohistochemistry-Paraffin: CCR8 Antibody [NB100-709] - Section of mouse spleen.](http://images.novusbio.com/fullsize/CCR8-Antibody-Immunohistochemistry-Paraffin-NB100-709-img0002.jpg "Immunohistochemistry-Paraffin: CCR8 Antibody [NB100-709] - Section of mouse spleen.")
![Immunocytochemistry/Immunofluorescence: WASF2 Antibody [NBP3-23200] - Immunocytochemical labeling of WASF2 in rat PC12 cells differentiated with NGF. The cells were labeled with rabbit polyclonal WASF2 (Central) antibody, then detected using appropriate secondary antibody conjugated to Cy3. The antibody was used in the absence (left) or presence (right) of blocking peptide.](http://images.novusbio.com/fullsize/nbp3-23200_rabbit-wasf2-pab-19920231856969.jpg "Immunocytochemistry/Immunofluorescence: WASF2 Antibody [NBP3-23200] - Immunocytochemical labeling of WASF2 in rat PC12 cells differentiated with NGF. The cells were labeled with rabbit polyclonal WASF2 (Central) antibody, then detected using appropriate secondary antibody conjugated to Cy3. The antibody was used in the absence (left) or presence (right) of blocking peptide.")
![Western Blot: WASF2 Antibody [NBP3-23200] - Western blot of rat PC12 lysate. The blots were probed with anti-WASF2 (Central region) in the presence (lane 2) or absence (lane 1) of WASF2 (Central region) blocking peptide.](http://images.novusbio.com/fullsize/nbp3-23200_rabbit-wasf2-pab-11920231633168.jpg)
![Immunohistochemistry: CEACAM5/CD66e Antibody (Arcitumomab) [NBP2-75904] - Formalin fixed human endometrial cancer slices were were stained with a NBP2-75904 at 5 ug/ml.](http://images.novusbio.com/fullsize/CEACAM5-CD66e-Antibody-Arcitumomab-Immunohistochemistry-NBP2-75904-img0002.jpg "Immunohistochemistry: CEACAM5/CD66e Antibody (Arcitumomab) [NBP2-75904] - Formalin fixed human endometrial cancer slices were were stained with a NBP2-75904 at 5 ug/ml.")
![Immunocytochemistry /Immunofluorescence: CEACAM5/CD66e Antibody (Arcitumomab) - Azide and BSA Free [NBP2-75904] - Formaldehyde-fixed rat pancreas slices were stained with NBP2-75904 at 5 ug/ml and detected with a FITC-conjugated secondary antibody. NBP2-75904 shows cross-reactivity with rat.](http://images.novusbio.com/fullsize/nbp2-75904_human-monoclonal-ceacam5-cd66e-antibody-arcitumomab-74202522141220.png)
![Immunocytochemistry/Immunofluorescence: CCRL2/CRAM-A/B Antibody (BZ2E3) - Chimeric [NBP3-11982] - Immunofluorescence analysis of paraformaldehyde fixed RAW264.7 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of BZ2E3 (NBP3-11982) 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 NBP3-11982, 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/CCRL2-CRAM-A-B-Antibody-BZ2E3-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-11982-img0001.jpg "Immunocytochemistry/Immunofluorescence: CCRL2/CRAM-A/B Antibody (BZ2E3) - Chimeric [NBP3-11982] - Immunofluorescence analysis of paraformaldehyde fixed RAW264.7 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of BZ2E3 (NBP3-11982) 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 NBP3-11982, 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.")
![Western Blot: Plexin A1 Antibody [NBP3-23317] - Western blots showing mouse brain (lanes 1 & 4), and Cos-7 cells untransfected (lanes 2 & 5) or transfected with mouse myc-tagged Plexin A1 (lanes 3 & 6). The blots were probed with either affinity purified anti-Plexin A1 (NBP3-23317); lanes 1-3) or with mouse monoclonal anti-Myc (lanes 4-6).](http://images.novusbio.com/fullsize/nbp3-23317_rabbit-plexin-a1-pab-199202312523643.jpg "Western Blot: Plexin A1 Antibody [NBP3-23317] - Western blots showing mouse brain (lanes 1 & 4), and Cos-7 cells untransfected (lanes 2 & 5) or transfected with mouse myc-tagged Plexin A1 (lanes 3 & 6). The blots were probed with either affinity purified anti-Plexin A1 (NBP3-23317); lanes 1-3) or with mouse monoclonal anti-Myc (lanes 4-6).")
![Immunocytochemistry/Immunofluorescence: Plexin A1 Antibody [NBP3-23317] - Immunocytochemical double labeling using anti-Myc mouse monoclonal and anti-Plexin A1 rabbit polyclonal (NBP3-23317) antibodies in Cos-7 cells mock transfected (A,D) or transfected with Myc-tagged mouse Plexin A1 construct (B,E). The specificity of the binding in E was demonstrated by using Plexin A1 peptide in the presence of this anti-Plexin A1 antibody (C,F).](http://images.novusbio.com/fullsize/nbp3-23317_rabbit-plexin-a1-pab-19920231856967.jpg)
![Western Blot: CCR5 [p Ser349] Antibody (E11/19) - Chimeric [NBP3-11995] - Molt4 cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of E11/19 (NBP3-11995) at 0.1 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/CCR5-p-Ser349-Antibody-E11-19-Chimeric-Western-Blot-NBP3-11995-img0001.jpg "Western Blot: CCR5 [p Ser349] Antibody (E11/19) - Chimeric [NBP3-11995] - Molt4 cell lysate (35ug protein in RIPA buffer) was resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of E11/19 (NBP3-11995) at 0.1 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: CCR5 [p Ser349] Antibody (E11/19) - Chimeric [NBP3-11995] - Immunofluorescence analysis of paraformaldehyde fixed U937 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of E11/19 (NBP3-11995) 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 NBP3-11995, 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/CCR5-p-Ser349-Antibody-E11-19-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-11995-img0002.jpg)
![Flow Cytometry: CCR5 [p Ser349] Antibody (E11/19) - Chimeric - Azide and BSA Free [NBP3-11995] - U937 cells were fixed using 2% PFA and stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-11995 (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/nbp3-11995_rabbit-monoclonal-ccr5-p-ser349-antibody-e11-19-chimeric-7420252226528.png)
![Western Blot: CCR5 Antibody (RC-10) - Chimeric [NBP3-12000] - Jurkat (A), Molt4 (B), K562 (C) and Daudi (D) cell lysates (35ug protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of RC-10 (NBP3-12000) at 0.0003 ug/ml, 0.001 ug/ml, 0.003 ug/ml and unknown ug/ml, respectively, 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/CCR5-Antibody-RC-10-Chimeric-Western-Blot-NBP3-12000-img0001.jpg "Western Blot: CCR5 Antibody (RC-10) - Chimeric [NBP3-12000] - Jurkat (A), Molt4 (B), K562 (C) and Daudi (D) cell lysates (35ug protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of RC-10 (NBP3-12000) at 0.0003 ug/ml, 0.001 ug/ml, 0.003 ug/ml and unknown ug/ml, respectively, before detection using an anti-rabbit secondary antibody. A primary incubation of 1h was used and protein was detected by chemiluminescence.")
![Immunocytochemistry/Immunofluorescence: CCR5 Antibody (RC-10) - Chimeric [NBP3-12000] - Immunofluorescence analysis of paraformaldehyde fixed U937 cells on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of RC-10 (NBP3-12000) 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 NBP3-12000, 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/CCR5-Antibody-RC-10-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12000-img0002.jpg)
![Flow Cytometry: CCR5 Antibody (RC-10) - Chimeric - Azide and BSA Free [NBP3-12000] - Paraformaldehyde fixed human peripheral blood monocytes permeabilized with 0.5% Triton were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-12000 (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/nbp3-12000_rabbit-monoclonal-ccr5-antibody-rc-10-chimeric-7420252214129.png)
![SDS-Page: Rat IL-1 alpha/IL-1F1 Protein [NBP2-35227]](http://images.novusbio.com/fullsize/Rat-IL-1-alpha-IL-1F1-Protein-SDS-Page-NBP2-35227-img0001.jpg "SDS-Page: Rat IL-1 alpha/IL-1F1 Protein [NBP2-35227]")
![Immunocytochemistry/Immunofluorescence: NKG2D/CD314 Antibody (6E5A7) - Chimeric - Azide and BSA Free [NBP3-20156] - Immunofluorescence analysis of paraformaldehyde fixed human peripheral blood leukocytes stained with the chimeric rabbit IgG version of 6E5A7 (NBP3-20156) (1:1000 dilution) for 1h followed by Alexa Fluor(R) 488 secondary antibody (1:1500 dilution), showing nuclear staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-20156, DAPI, merged channels and an isotype control. The isotype control was anti-fluorescein antibody (NBP2-52638) followed by staining with Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-20156_rabbit-nkg2d-cd314-mab-6e5a7-chimeric-azide-bsa-free-2742023924240.png "Immunocytochemistry/Immunofluorescence: NKG2D/CD314 Antibody (6E5A7) - Chimeric - Azide and BSA Free [NBP3-20156] - Immunofluorescence analysis of paraformaldehyde fixed human peripheral blood leukocytes stained with the chimeric rabbit IgG version of 6E5A7 (NBP3-20156) (1:1000 dilution) for 1h followed by Alexa Fluor(R) 488 secondary antibody (1:1500 dilution), showing nuclear staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-20156, DAPI, merged channels and an isotype control. The isotype control was anti-fluorescein antibody (NBP2-52638) followed by staining with Alexa Fluor(R) 488 secondary antibody.")
![Western Blot: NKG2D/CD314 Antibody (6E5A7) - Chimeric - Azide and BSA Free [NBP3-20156] - K562(A) (2ug/ml) and human peripheral blood monocytes(B) (2ug/ml) cells lysate (35ug protein in RIPA buffer) were resolved on a SDS PAGE gel and blots were probed with the chimeric rabbit version of 6E5A7 (NBP3-20156) 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/nbp3-20156_rabbit-nkg2d-cd314-mab-6e5a7-chimeric-azide-bsa-free-2742023924251.png)