| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-93173-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP2-94877-0.02ml | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-06531-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-12008-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26302-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-26521-50ul | |||
![Western Blot: Serine racemase Antibody [NBP2-93173] - Analysis of extracts of various cell lines, using SRR antibody at 1:3000 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/Serine-racemase-Antibody-Western-Blot-NBP2-93173-img0001.jpg "Western Blot: Serine racemase Antibody [NBP2-93173] - Analysis of extracts of various cell lines, using SRR antibody at 1:3000 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.")
![Western Blot: SH3GL3 Antibody [NBP2-94877] - Analysis of extracts of various cell lines, using SH3GL3 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: 1s.](http://images.novusbio.com/fullsize/SH3GL3-Antibody-Western-Blot-NBP2-94877-img0001.jpg "Western Blot: SH3GL3 Antibody [NBP2-94877] - Analysis of extracts of various cell lines, using SH3GL3 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: 1s.")
![Western Blot: NAPA Antibody (7Z6F6) [NBP3-15691] - Western blot analysis of extracts of various cell lines, using NAPA antibody (NBP3-15691) 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: 30s.](http://images.novusbio.com/fullsize/NAPA-Antibody-7Z6F6-Western-Blot-NBP3-15691-img0001.jpg "Western Blot: NAPA Antibody (7Z6F6) [NBP3-15691] - Western blot analysis of extracts of various cell lines, using NAPA antibody (NBP3-15691) 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: 30s.")
![Western Blot: Synaptojanin 1 Antibody (5H1) [NBP1-47559] - Rat Hippocampal Lysate showing specific immunolabeling of the ~145k Synaptojanin protein.](http://images.novusbio.com/fullsize/Synaptojanin-1-Antibody-5H1-Western-Blot-NBP1-47559-img0001.jpg "Western Blot: Synaptojanin 1 Antibody (5H1) [NBP1-47559] - Rat Hippocampal Lysate showing specific immunolabeling of the ~145k Synaptojanin protein.")
![Immunohistochemistry-Paraffin: LMX1b Antibody [NBP3-06531] - Staining of human LMX1B in human testis with rabbit polyclonal antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/LMX1b-Antibody-Immunohistochemistry-Paraffin-NBP3-06531-img0002.jpg "Immunohistochemistry-Paraffin: LMX1b Antibody [NBP3-06531] - Staining of human LMX1B in human testis with rabbit polyclonal antibody at 1:100 dilution.")
![Immunohistochemistry-Paraffin: LMX1b Antibody [NBP3-06531] - Staining of human LMX1B in human brain with rabbit polyclonal antibody at 1:100 dilution.](http://images.novusbio.com/fullsize/LMX1b-Antibody-Immunohistochemistry-Paraffin-NBP3-06531-img0001.jpg)
![Immunocytochemistry /Immunofluorescence: beta-2 Adrenergic R/ADRB2 Antibody (13D6) - Chimeric - Azide and BSA Free [NBP3-12008] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on Shi-fix(TM) coverslips stained with NBP3-12008 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: NBP3-12008, 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/nbp3-12008_rabbit-monoclonal-beta-2-adrenergic-r-adrb2-antibody-13d6-chimeric-7420252211307.png "Immunocytochemistry /Immunofluorescence: beta-2 Adrenergic R/ADRB2 Antibody (13D6) - Chimeric - Azide and BSA Free [NBP3-12008] - Immunofluorescence analysis of paraformaldehyde fixed HepG2 cells on Shi-fix(TM) coverslips stained with NBP3-12008 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: NBP3-12008, 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: eNOS Antibody [NBP3-23180] - Western blot analysis of human umbilical vein endothelial cells treated with calyculin A (100 nM) for 30 min. (lanes 1, 3, 5 & 7) then the blots were treated with lambda phosphatase (lanes 2, 4, 6 & 8). The blots were probed with anti-endothelial nitric oxide synthase (eNOS) (C-terminal region) (lanes 1 & 2), anti-eNOS (Ser-632) (lanes 3 & 4), anti-eNOS (Ser-1177) (lanes 5 & 6) and anti-eNOS (a.a. 1172-1181) (lanes 7 & 8).](http://images.novusbio.com/fullsize/nbp3-23180_rabbit-enos-pab-19920231759442.jpg "Western Blot: eNOS Antibody [NBP3-23180] - Western blot analysis of human umbilical vein endothelial cells treated with calyculin A (100 nM) for 30 min. (lanes 1, 3, 5 & 7) then the blots were treated with lambda phosphatase (lanes 2, 4, 6 & 8). The blots were probed with anti-endothelial nitric oxide synthase (eNOS) (C-terminal region) (lanes 1 & 2), anti-eNOS (Ser-632) (lanes 3 & 4), anti-eNOS (Ser-1177) (lanes 5 & 6) and anti-eNOS (a.a. 1172-1181) (lanes 7 & 8).")
![Western Blot: eNOS [p Ser632] Antibody (M232) [NBP3-23181] - Western blot analysis of human umbilical vein endothelial cells stimulated with Calyculin A and untreated (lanes 1, 3, 5) or treated (lanes 2, 4, 6) with lambda phosphatase. The blots were probed with anti-endothelial Nitric Oxide Synthase (eNOS) monoclonal antibody (lanes 1 & 2), anti-eNOS (Ser-632) phospho-specific antibody (lanes 3 & 4), and anti-eNOS polyclonal antibody (lanes 5 & 6).](http://images.novusbio.com/fullsize/nbp3-23181_mouse-enos-p-ser632-mab-m232-11920231665313.jpg "Western Blot: eNOS [p Ser632] Antibody (M232) [NBP3-23181] - Western blot analysis of human umbilical vein endothelial cells stimulated with Calyculin A and untreated (lanes 1, 3, 5) or treated (lanes 2, 4, 6) with lambda phosphatase. The blots were probed with anti-endothelial Nitric Oxide Synthase (eNOS) monoclonal antibody (lanes 1 & 2), anti-eNOS (Ser-632) phospho-specific antibody (lanes 3 & 4), and anti-eNOS polyclonal antibody (lanes 5 & 6).")
![Western Blot: Serine racemase Antibody (12B2) [NBP3-26302] - Positive Western Blot detected in: A549 whole cell lysate, U87 whole cell lysate. All lanes: Serine racemase Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 37 kDa Observed band size: 37 kDa](http://images.novusbio.com/fullsize/nbp3-26302_rabbit-serine-racemase-mab-12b2-282202411485833.jpg "Western Blot: Serine racemase Antibody (12B2) [NBP3-26302] - Positive Western Blot detected in: A549 whole cell lysate, U87 whole cell lysate. All lanes: Serine racemase Antibody at 1: 1000 Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 37 kDa Observed band size: 37 kDa")
![Flow Cytometry: Serine racemase Antibody (12B2) [NBP3-26302] - Overlay Peak curve showing HepG2 cells stained with Serine racemase Antibody (12B2) (red line) at 1:100. 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/nbp3-26302_rabbit-serine-racemase-mab-12b2-282202414183615.jpg)
![Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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/nbp3-26521_rabbit-beta-2-adrenergic-r-adrb2-mab-4c11-262202415253325.jpg "Immunohistochemistry: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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: beta-2 Adrenergic R/ADRB2 Antibody (4C11) [NBP3-26521] - Image of beta-2 Adrenergic R/ADRB2 Antibody (4C11) diluted at 1:100 and staining in paraffin-embedded human endometrial 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/nbp3-26521_rabbit-beta-2-adrenergic-r-adrb2-mab-4c11-262202415253314.jpg)