| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB100-64770-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP1-22492-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-97038-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12005-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-75192-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26159-50ul | |||
![Flow Cytometry: IL6R Antibody (B-R6) [NB100-64770] - A surface stain was performed on human peripheral blood lymphocytes with IL6R (B-R6) antibody NB100-64770 (blue) and a matched isotype control NBP2-27287 (orange). Cells were incubated in an antibody dilution of 1 ug/mL for 20 minutes at room temperature, followed by mouse F(ab)2 IgG (H+L) APC-conjugated secondary antibody (F0101B, R&D Systems). A co-stain was performed with NBP2-24867AF488.](http://images.novusbio.com/fullsize/IL6R-Antibody-B-R6-Flow-Cytometry-NB100-64770-img0001.jpg "Flow Cytometry: IL6R Antibody (B-R6) [NB100-64770] - A surface stain was performed on human peripheral blood lymphocytes with IL6R (B-R6) antibody NB100-64770 (blue) and a matched isotype control NBP2-27287 (orange). Cells were incubated in an antibody dilution of 1 ug/mL for 20 minutes at room temperature, followed by mouse F(ab)2 IgG (H+L) APC-conjugated secondary antibody (F0101B, R&D Systems). A co-stain was performed with NBP2-24867AF488.")
![Western Blot: PSG-1 Antibody [NBP1-58028] - NCI-H226 cell lysate, concentration 2.5 ug/ml.](http://images.novusbio.com/fullsize/PSG-1-Antibody-Western-Blot-NBP1-58028-img0003.jpg "Western Blot: PSG-1 Antibody [NBP1-58028] - NCI-H226 cell lysate, concentration 2.5 ug/ml.")
![Western Blot: LYVE-1 Antibody (4G7C3) [NBP3-16385] - Western blot analysis of extracts of various cell lines, using LYVE-1 Rabbit mAb (NBP3-16385) 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: 60s.](http://images.novusbio.com/fullsize/LYVE-1-Antibody-4G7C3-Western-Blot-NBP3-16385-img0001.jpg "Western Blot: LYVE-1 Antibody (4G7C3) [NBP3-16385] - Western blot analysis of extracts of various cell lines, using LYVE-1 Rabbit mAb (NBP3-16385) 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: 60s.")
![Immunohistochemistry-Paraffin: PSG1 Antibody [NBP2-97038] - Immunochemical staining of human PSG1 in human placenta with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/PSG1-Antibody-Immunohistochemistry-Paraffin-NBP2-97038-img0002.jpg "Immunohistochemistry-Paraffin: PSG1 Antibody [NBP2-97038] - Immunochemical staining of human PSG1 in human placenta with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.")
![Immunohistochemistry-Paraffin: PSG1 Antibody [NBP2-97038] - Immunochemical staining of human PSG1 in human kidney with rabbit polyclonal antibody at 1:1000 dilution, formalin-fixed paraffin embedded sections.](http://images.novusbio.com/fullsize/PSG1-Antibody-Immunohistochemistry-Paraffin-NBP2-97038-img0001.jpg)
![Immunocytochemistry/Immunofluorescence: CXCR2/IL-8RB Antibody (HC2) - Chimeric [NBP3-12005] - Immunofluorescence analysis of paraformaldehyde fixed human peripheral blood leukocytes on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of HC2 (NBP3-12005) 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 NBP3-12005, 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/CXCR2-IL-8RB-Antibody-HC2-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-12005-img0001.jpg "Immunocytochemistry/Immunofluorescence: CXCR2/IL-8RB Antibody (HC2) - Chimeric [NBP3-12005] - Immunofluorescence analysis of paraformaldehyde fixed human peripheral blood leukocytes on Shi-fix(TM) coverslips stained with the chimeric rabbit IgG version of HC2 (NBP3-12005) 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 NBP3-12005, 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: CXCR2/IL-8RB Antibody (HC2) - Chimeric - Azide and BSA Free [NBP3-12005] - Paraformaldehyde fixed human peripheral blood monocytes were stained with anti-unknown specificity antibody (isotype control, black line) or NBP3-12005 (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/nbp3-12005_rabbit-monoclonal-cxcr2-il-8rb-antibody-hc2-chimeric-74202522113042.png)
![Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) 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 505-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241249369.jpg "Immunocytochemistry/Immunofluorescence: LYVE-1 Antibody (11C11) [NBP3-26159] - Staining of HepG2 with LYVE-1 Antibody (11C11) 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 505-conjugated Goat Anti-Rabbit IgG (H+L).")
![Flow Cytometry: LYVE-1 Antibody (11C11) [NBP3-26159] - Overlay Peak curve showing HepG2 cells stained with LYVE-1 Antibody (11C11) (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/nbp3-26159_rabbit-lyve-1-mab-11c11-28220241418361.jpg)
![Western Blot: TCF-12/HTF4 Antibody [NB100-2338] - Detection of Human TCF12 on HeLa whole cell lysate using NB100-2338. TCF12 was also immunoprecipitated using rabbit anti-TCF12 antibody NB100-2337.](http://images.novusbio.com/fullsize/TCF-12-HTF4-Antibody-Western-Blot-NB100-2338-img0003.jpg "<b>Independent Antibodies Validation. </b>Western Blot: TCF-12/HTF4 Antibody [NB100-2338] - Detection of Human TCF12 on HeLa whole cell lysate using NB100-2338. TCF12 was also immunoprecipitated using rabbit anti-TCF12 antibody NB100-2337.")
