| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Carrier-Free | NBP2-35234-10ug | |||
| Carrier-Free | NBP2-35234-500ug | |||
| Carrier-Free | NBP2-35234-1000ug | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-09045-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26509-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26159-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26432-50ul | |||
![Western Blot: Actin (Muscle Specific) Antibody (3G8C7A6) - Chimeric - BSA Free [NBP3-43563] - HEK293 (A) (1µg/ml), HeLa (B) (0.1µg/ml) cells lysate, and human skeletal muscle (C) (0.01µg/ml) tissue lysate (35µg protein in RIPA buffer) were resolved on an SDS-PAGE gel, and blots were probed with NBP3-43563 at the mentioned respective concentrations before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and protein was detected by chemiluminescence.](http://images.novusbio.com/fullsize/nbp3-48433_rb-dccov-nucleoprotein-pab-hku23-368f-azide-bsa-free-western-blot-2220260311814.png "Western Blot: Actin (Muscle Specific) Antibody (3G8C7A6) - Chimeric - BSA Free [NBP3-43563] - HEK293 (A) (1µg/ml), HeLa (B) (0.1µg/ml) cells lysate, and human skeletal muscle (C) (0.01µg/ml) tissue lysate (35µg protein in RIPA buffer) were resolved on an SDS-PAGE gel, and blots were probed with NBP3-43563 at the mentioned respective concentrations before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and protein was detected by chemiluminescence.")
![Flow Cytometry: Actin (Muscle Specific) Antibody (3G8C7A6) - Chimeric - BSA Free [NBP3-43563] - Paraformaldehyde fixed HeLa cells permeabilized with 0.5% Triton were stained with the anti-unknown specificity antibody (isotype control, black line) or NBP3-43563 (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 the cells were analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/nbp3-43563_rb-actin-muscle-specific-mab-3g8c7a6-chimeric-azide-bsa-free-flow-cytometry-2220260355517.png)
![Immunocytochemistry/ Immunofluorescence: Actin (Muscle Specific) Antibody (3G8C7A6) - Chimeric - BSA Free [NBP3-43563] - Immunofluorescence analysis of paraformaldehyde fixed HeLa cells, permeabilized with 0.15% Triton, on coverslips stained with NBP3-43563 (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, NBP3-43563, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody followed by staining with Alexa Fluor® 488 secondary antibody.](http://images.novusbio.com/fullsize/nbp3-43563_rb-actin-muscle-specific-mab-3g8c7a6-chimeric-azide-bsa-free-immunocytochemistry-immunofluorescence-2220260355519.png)
![SDS-Page: Porcine CXCL8/IL-8 Protein [NBP2-35234]](http://images.novusbio.com/fullsize/Porcine-CXCL8-IL-8-Protein-SDS-Page-NBP2-35234-img0001.jpg "SDS-Page: Porcine CXCL8/IL-8 Protein [NBP2-35234]")
![Immunocytochemistry/Immunofluorescence: TWEAK/TNFSF12 Antibody (MTW-1) - Chimeric [NBP3-09045] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes immobilized on Shi-fix(TM) cover-slips and stained with the chimeric rabbit IgG version of MTW-1 (NBP3-09045) at 10 ug/ml followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining in subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-09045, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody followed by Alexa Fluor(R) 488 secondary antibody.](http://images.novusbio.com/fullsize/TWEAK-TNFSF12-Antibody-MTW-1-Chimeric-Immunocytochemistry-Immunofluorescence-NBP3-09045-img0001.jpg "Immunocytochemistry/Immunofluorescence: TWEAK/TNFSF12 Antibody (MTW-1) - Chimeric [NBP3-09045] - Immunofluorescence analysis of paraformaldehyde fixed mouse splenocytes immobilized on Shi-fix(TM) cover-slips and stained with the chimeric rabbit IgG version of MTW-1 (NBP3-09045) at 10 ug/ml followed by Alexa Fluor(R) 488 secondary antibody (2 ug/ml), showing membrane staining in subset of cells. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom NBP3-09045, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody followed by Alexa Fluor(R) 488 secondary antibody.")
![Western Blot: SHP-2/PTPN11 Antibody (M163) [NBP3-23400] - Western blot analysis of adult mouse brain. The blot was probed with anti-SHP2 (N-terminal) antibody at 1:250 (lane 1), 1:500 (lane 2), 1:1000 (lane 3), and 1:2000 (lane 4).](http://images.novusbio.com/fullsize/nbp3-23400_mouse-shp-2-ptpn11-mab-m163-19920231410139.jpg "Western Blot: SHP-2/PTPN11 Antibody (M163) [NBP3-23400] - Western blot analysis of adult mouse brain. The blot was probed with anti-SHP2 (N-terminal) antibody at 1:250 (lane 1), 1:500 (lane 2), 1:1000 (lane 3), and 1:2000 (lane 4).")
![Western Blot: ER alpha/NR3A1 Antibody (ER505) - Azide and BSA Free [NBP2-33106] - Western blot analysis of Estrogen Receptor in MCF-7 lysate using Estrogen Receptor Ab (ER505).](http://images.novusbio.com/fullsize/ER-alpha-NR3A1-Antibody-ER505-Azide-and-BSA-Free-Western-Blot-NBP2-33106-img0003.jpg "Western Blot: ER alpha/NR3A1 Antibody (ER505) - Azide and BSA Free [NBP2-33106] - Western blot analysis of Estrogen Receptor in MCF-7 lysate using Estrogen Receptor Ab (ER505).")
![Immunohistochemistry: Angiopoietin-2 Antibody (1F10) [NBP3-26509] - Image of Angiopoietin-2 Antibody (1F10) diluted at 1:100 and staining in paraffin-embedded human liver cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26509_rabbit-angiopoietin-2-mab-1f10-262202414471528.jpg "Immunohistochemistry: Angiopoietin-2 Antibody (1F10) [NBP3-26509] - Image of Angiopoietin-2 Antibody (1F10) diluted at 1:100 and staining in paraffin-embedded human liver cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: Angiopoietin-2 Antibody (1F10) [NBP3-26509] - Image of Angiopoietin-2 Antibody (1F10) diluted at 1:100 and staining in paraffin-embedded human liver cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26509_rabbit-angiopoietin-2-mab-1f10-262202414471537.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).](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)
![Immunohistochemistry: PLGF Antibody (1B6) [NBP3-26432] - Image of PLGF Antibody (1B6) diluted at 1:100 and staining in paraffin-embedded human colon cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26432_rabbit-plgf-mab-1b6-262202414471590.jpg "Immunohistochemistry: PLGF Antibody (1B6) [NBP3-26432] - Image of PLGF Antibody (1B6) diluted at 1:100 and staining in paraffin-embedded human colon cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.")
![Immunohistochemistry: PLGF Antibody (1B6) [NBP3-26432] - Image of PLGF Antibody (1B6) diluted at 1:100 and staining in paraffin-embedded human colon cancer performed. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.](http://images.novusbio.com/fullsize/nbp3-26432_rabbit-plgf-mab-1b6-26220241422528.jpg)
![Immunohistochemistry-Paraffin: TGF-beta 3 Antibody (C15) [NBP3-41629] - DAB staining on IHC-P; Sample: Human Cerebrum Tissue; Primary Ab: 30ug/ml NBP3-41629; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody](http://images.novusbio.com/fullsize/nbp3-41629_mouse-tgf-beta-3-mab-c15-612202421331632.jpg "Immunohistochemistry-Paraffin: TGF-beta 3 Antibody (C15) [NBP3-41629] - DAB staining on IHC-P; Sample: Human Cerebrum Tissue; Primary Ab: 30ug/ml NBP3-41629; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody")
![Western Blot: TGFBI Antibody [NBP2-20613] - Sample (30 ug of whole cell lysate) A: Hela 7. 5% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/TGFBI-Antibody-Western-Blot-NBP2-20613-img0001.jpg "Western Blot: TGFBI Antibody [NBP2-20613] - Sample (30 ug of whole cell lysate) A: Hela 7. 5% SDS PAGE gel, diluted at 1:1000.")