| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NB300-169SS | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-11826-0.025mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-06485-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP3-05805-50ul | |||
![Western Blot: Parkin Antibody [NB600-1540] - Western blot of HEK293t cell lysate expressing FLAG-tagged recombinant human Parkin detected using NB600-1540 at various dilutions (1:2,000, B-1:5,000, C-1:10,000). ECL exposure 1min. FLAG-tagged Parkin courtesy of Dr P.A. Robinson, University of Leeds, UK).](http://images.novusbio.com/fullsize/p_17998_1.jpg "Western Blot: Parkin Antibody [NB600-1540] - Western blot of HEK293t cell lysate expressing FLAG-tagged recombinant human Parkin detected using NB600-1540 at various dilutions (1:2,000, B-1:5,000, C-1:10,000). ECL exposure 1min. FLAG-tagged Parkin courtesy of Dr P.A. Robinson, University of Leeds, UK).")
![Western Blot: Pallidin Antibody (15G2) [NB120-13261] - Analysis of Syntaxin 13 (15G2), mAb : Lane 1: MW Marker, Lane 2: Rat Brain Lysate Lane 3: Mouse Brain Lysate, Lane 4: CHO-K1 Cell Lysate (Heat Shocked)](http://images.novusbio.com/fullsize/Pallidin-Antibody-15G2-Western-Blot-NB120-13261-img0002.jpg "Western Blot: Pallidin Antibody (15G2) [NB120-13261] - Analysis of Syntaxin 13 (15G2), mAb : Lane 1: MW Marker, Lane 2: Rat Brain Lysate Lane 3: Mouse Brain Lysate, Lane 4: CHO-K1 Cell Lysate (Heat Shocked)")
![Immunohistochemistry-Paraffin: Pallidin Antibody (15G2) [NB120-13261] - Analysis of human placenta tissue stained with Syntaxin 13, mAb (15G2) at 20 ug/ml.](http://images.novusbio.com/fullsize/Pallidin-Antibody-15G2-Immunohistochemistry-Paraffin-NB120-13261-img0001.jpg)
![Western Blot: NPFFR2 Antibody [NB300-169] - Analysis of human NPFF2 in brain lysate using this antibody at a dilution of 1:500](http://images.novusbio.com/fullsize/NPFFR2-Antibody-Western-Blot-NB300-169-img0001.jpg "Western Blot: NPFFR2 Antibody [NB300-169] - Analysis of human NPFF2 in brain lysate using this antibody at a dilution of 1:500")
![Immunohistochemistry-Paraffin: NrCAM Antibody (MM0495-8E25) [NBP2-11826] - 10% Buffer formalin fixed and parffine embedded human placetal tissue section (4um) is subjected IHC staining using NBP2-11826. Tissue section was pretreated in citric buffer (pH 6.0) with microwave for antige retrieval before IHC is applied.](http://images.novusbio.com/fullsize/NrCAM-Antibody-MM0495-8E25-Immunohistochemistry-Paraffin-NBP2-11826-img0001.jpg "<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: NrCAM Antibody (MM0495-8E25) [NBP2-11826] - 10% Buffer formalin fixed and parffine embedded human placetal tissue section (4um) is subjected IHC staining using NBP2-11826. Tissue section was pretreated in citric buffer (pH 6.0) with microwave for antige retrieval before IHC is applied.")
![Immunohistochemistry: NK2R Antibody [NBP3-14421] - Immunohistochemistry of breast carcinoma](http://images.novusbio.com/fullsize/NK2R-Antibody-Immunohistochemistry-NBP3-14421-img0004.jpg "Immunohistochemistry: NK2R Antibody [NBP3-14421] - Immunohistochemistry of breast carcinoma")
![Immunohistochemistry-Paraffin: NK2R Antibody [NBP3-14421] - Immunohistochemistry of formalin-fixed, paraffin-embedded human breast carcinoma after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/NK2R-Antibody-Immunohistochemistry-Paraffin-NBP3-14421-img0001.jpg)
![Immunohistochemistry-Paraffin: NK2R Antibody [NBP3-14421] - Immunohistochemistry of formalin-fixed, paraffin-embedded human small intestine, muscularis propria, after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/NK2R-Antibody-Immunohistochemistry-Paraffin-NBP3-14421-img0002.jpg)
![Immunohistochemistry-Paraffin: NK2R Antibody [NBP3-14421] - Immunohistochemistry of formalin-fixed, paraffin-embedded human colon after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/NK2R-Antibody-Immunohistochemistry-Paraffin-NBP3-14421-img0003.jpg)
![Immunohistochemistry: NK2R Antibody [NBP3-14421] - Immunohistochemistry of ovary carcinoma](http://images.novusbio.com/fullsize/NK2R Antibody-Immunohistochemistry-NBP3-14421-img0005.jpg)
![ELISA: Human Myelin Protein Zero ELISA Kit (Colorimetric) [NBP3-40278] - Standard Curve Reference](http://images.novusbio.com/fullsize/nbp3-40278_human-myelin-protein-zero-elisa-kit-colorimetric-2110202415343964.png "ELISA: Human Myelin Protein Zero ELISA Kit (Colorimetric) [NBP3-40278] - Standard Curve Reference")
![Immunohistochemistry-Paraffin: 5-HT2B Antibody [NLS1187] - Brain, Amygdala neurons](http://images.novusbio.com/fullsize/5-HT2B-Antibody-Immunohistochemistry-Paraffin-NLS1187-img0008.jpg "Immunohistochemistry-Paraffin: 5-HT2B Antibody [NLS1187] - Brain, Amygdala neurons")
![Immunohistochemistry-Paraffin: 5-HT2B Antibody [NLS1187] - Analysis of anti-5HT2B Receptor antibody with human brain, neurons and glia.](http://images.novusbio.com/fullsize/5-HT2B-Antibody-Immunohistochemistry-Paraffin-NLS1187-img0003.jpg)
![Immunohistochemistry-Paraffin: 5-HT2B Antibody [NLS1187] - Anti-HTR1B / 5-HT2B Receptor antibody IHC of human Brain, Glioblastoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/5-HT2B-Antibody-Immunohistochemistry-Paraffin-NLS1187-img0005.jpg)
![Immunohistochemistry-Paraffin: 5-HT2B Antibody [NLS1187] - Human Lung, Small Cell Carcinoma. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.](http://images.novusbio.com/fullsize/5-HT2B-Antibody-Immunohistochemistry-Paraffin-NLS1187-img0006.jpg)
![Immunohistochemistry-Paraffin: 5-HT2B Antibody [NLS1187] - Brain, Substantia Nigra](http://images.novusbio.com/fullsize/5-HT2B-Antibody-Immunohistochemistry-Paraffin-NLS1187-img0007.jpg)
![Western Blot: CaMKV Antibody [NBP3-06485] - Lane A: HepG2 Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:54 kDaObserved band size:54 kDa](http://images.novusbio.com/fullsize/CaMKV-Antibody-Western-Blot-NBP3-06485-img0001.jpg "Western Blot: CaMKV Antibody [NBP3-06485] - Lane A: HepG2 Whole Cell LysateLysates/proteins at 30 ug per lane.SecondaryGoat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution.Developed using the ECL technique.Performed under reducing conditions.Predicted band size:54 kDaObserved band size:54 kDa")
![Immunoprecipitation: CaMKV Antibody [NBP3-06485] - Lane A:0.5 mg HepG2 Whole Cell Lysate1 uL anti-CAMKV rabbit polyclonal antibody and 60 ug of Immunomagnetic beads Protein A/G.Primary antibody:Anti-CAMKV rabbit polyclonal antibody,at 1:500 dilution Secondary antibody:Clean-Blot IP Detection Reagent (HRP) at 1:1000dilutionDeveloped using the ECL technique.Performed under reducing conditions.Predicted band size: 54 kDaObserved band size :54 kDa](http://images.novusbio.com/fullsize/CaMKV-Antibody-Immunoprecipitation-NBP3-06485-img0003.jpg)
![Immunocytochemistry/Immunofluorescence: CaMKV Antibody [NBP3-06485] - Staining of CAMKV in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.1% Triton X-100 in PBS,blocked with 10% serum, and incubated with NBP3-06485 antibody (dilution ratio 1:1000) at 4? overnight. Then cells were stained with the Alexa Fluor488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to Nucleus and Cytoplasm.](http://images.novusbio.com/fullsize/nbp3-06485_rabbit-polyclonal-camkv-antibody-2352025213514.png)
![Flow Cytometry: Park7/DJ-1 Antibody (007) [NBP3-05805] - Flow cytometric analysis of Human Park7/DJ-1 expression on HeLa cells. The cells were treated, stained with NBP3-05805, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-235202521451748.png "Flow Cytometry: Park7/DJ-1 Antibody (007) [NBP3-05805] - Flow cytometric analysis of Human Park7/DJ-1 expression on HeLa cells. The cells were treated, stained with NBP3-05805, then a FITC-conjugated second step antibody. The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![Immunocytochemistry/ Immunofluorescence: Park7/DJ-1 Antibody (007) [NBP3-05805] - Immunofluorescence staining of Human Park7/DJ-1 in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP3-05805 (1:60) at 37 1 hour. Then cells were stained with the Alexa Fluor 594-conjugated Goat Anti-rabbit IgG secondary antibody (red) and counterstained with DAPI (blue). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-23520251628125.png)
![Western Blot: Park7/DJ-1 Antibody (007) [NBP3-05805] - NBP3-05805 at 1:1000 dilution Lane A: Hela Whole Cell Lysate Lane B: Jurkat Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG H&L (Dylight800) at 1/10000 dilution. Developed using the Odyssey technique. Performed under reducing conditions. Predicted band size:20 kDa Observed band size:24 kDa](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-23520252135168.png)
![Immunoprecipitation: Park7/DJ-1 Antibody (007) [NBP3-05805] - PARK7 was immunoprecipitated using: Lane A:0.5 mg Jurkat Whole Cell Lysate Lane B:0.5 mg Hela Whole Cell Lysate Lane C:0.5 mg 293T Whole Cell Lysate 2 uL NBP3-05805 and 15 ul of 50 % Protein G agarose. Primary antibody: NBP3-05805, at 1:1000 dilution. Secondary antibody: Dylight 800-labeled antibody to rabbit IgG (H+L), at 1:5000 dilution. Developed using the odssey technique. Performed under reducing conditions. Predicted band size: 20 kDa Observed band size: 20 kDa](http://images.novusbio.com/fullsize/nbp3-05805_rabbit-monoclonal-park7-dj-1-antibody-007-235202514331514.png)
![Immunohistochemistry: Enolase 2/Neuron-specific Enolase Antibody (NSE-P2) [NBP3-30895] - Left and Center: Immunohistochemical staining of normal pancreas tissue (left) and small bowel tumor tissue (center) using NSE antibody (X2070M and NBP3-30895).Right: Western blot analysis using NSE antibodies (X2070M and NBP3-30895) on alpha and gamma enolase standards.](http://images.novusbio.com/fullsize/nbp3-30895_mouse-enolase-2-neuron-specific-enolase-mab-nse-p2-811202420594228.jpg "Immunohistochemistry: Enolase 2/Neuron-specific Enolase Antibody (NSE-P2) [NBP3-30895] - Left and Center: Immunohistochemical staining of normal pancreas tissue (left) and small bowel tumor tissue (center) using NSE antibody (X2070M and NBP3-30895).Right: Western blot analysis using NSE antibodies (X2070M and NBP3-30895) on alpha and gamma enolase standards.")
![Immunohistochemistry: Plexin B2 Antibody (PSH03-48) [NBP3-32828] - Immunohistochemical analysis of paraffin-embedded human colon cancer tissue with Rabbit anti-Plexin B2 antibody (NBP3-32828) at 1/2,000 dilution.<br/><br/> 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 (NBP3-32828) at 1/2,000 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/nbp3-32828_rabbit-plexin-b2-mab-psh03-48-298202414333638.jpg "Immunohistochemistry: Plexin B2 Antibody (PSH03-48) [NBP3-32828] - Immunohistochemical analysis of paraffin-embedded human colon cancer tissue with Rabbit anti-Plexin B2 antibody (NBP3-32828) at 1/2,000 dilution.<br/><br/> 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 (NBP3-32828) at 1/2,000 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.")
![Immunocytochemistry/ Immunofluorescence: Plexin B2 Antibody (PSH03-48) [NBP3-32828] - Immunocytochemistry analysis of HeLa cells labeling Plexin B2 with Rabbit anti-Plexin B2 antibody (NBP3-32828) at 1/100 dilution.<br/><br/> Cells were fixed in 100% precooled methanol for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-Plexin B2 antibody (NBP3-32828) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.<br/><br/> Beta tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.](http://images.novusbio.com/fullsize/nbp3-32828_rabbit-plexin-b2-mab-psh03-48-2920241192364.jpg)
![Western blot analysis on different lysates with NBP3-32828 at 1/2,000 dilution. Lane 1: LNCaP cell lysate Lane 2: 293T cell lysate Lane 3: HeLa cell lysate Lane 4: U-87 MG cell lysate Lane 5: HepG2 cell lysate Lane 6: K-562 cell lysate Lane 7: Jurkat cell lysate Lane 8: MCF7 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 205 kDa Observed band size: 170/240 kDa Exposure time: 43 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. NBP3-32828 at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ 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/nbp3-32828_-western-blot-639204597147954485.jpg)
![Immunohistochemistry-Frozen: APP Antibody (JE30-54) [NBP3-32034] - Immunofluorescence analysis of frozen mouse cerebral cortex tissue with Rabbit anti-APP antibody (NBP3-32034) at 1/200 dilution.<br/><br/>The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32034, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).](http://images.novusbio.com/fullsize/nbp3-32034_rabbit-app-mab-je30-54-2682024159394.jpg "Immunohistochemistry-Frozen: APP Antibody (JE30-54) [NBP3-32034] - Immunofluorescence analysis of frozen mouse cerebral cortex tissue with Rabbit anti-APP antibody (NBP3-32034) at 1/200 dilution.<br/><br/>The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32034, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).")
![Immunohistochemistry: APP Antibody (JE30-54) [NBP3-32034] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-APP antibody (NBP3-32034) at 1/1,000 dilution.<br/><br/> 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 (NBP3-32034) at 1/1,000 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/nbp3-32034_rabbit-app-mab-je30-54-298202414304185.jpg)
![Western blot analysis on different lysates with NBP3-32034 at 1/5,000 dilution. Lane 1: PC-3 cell lysate Lane 2: K-562 cell lysate (negative) Lane 3: Mouse brain tissue lysate Lane 4: Mouse skeletal muscle tissue lysate (negative) Lane 5: Rat brain tissue lysate Lane 6: Rat skeletal muscle tissue lysate (negative) Lysates/proteins at 20 µg/Lane. Predicted band size: 87 kDa Observed band size: 100 kDa Exposure time: 20 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. NBP3-32034 at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ 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/nbp3-32034_-western-blot-639204590071453637.jpg)