| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-98729-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-12668-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-90037-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89884-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-89368-100ul | |||
![Western Blot: ZEB1 Antibody (JE57-64) [NBP3-33111] - Western blot analysis of ZEB1 on different lysates with Rabbit anti-ZEB1 antibody (NBP3-33111) at 1/500 dilution. Lane 1: Hela cell lysate Lane 2: HUVEC cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 124 kDa Observed band size: 200 kDa Exposure time: 3 minutes; 6% 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 (NBP3-33111) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-33111_rabbit-zeb1-mab-je57-64-288202414191510.jpg "Western Blot: ZEB1 Antibody (JE57-64) [NBP3-33111] - Western blot analysis of ZEB1 on different lysates with Rabbit anti-ZEB1 antibody (NBP3-33111) at 1/500 dilution. Lane 1: Hela cell lysate Lane 2: HUVEC cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 124 kDa Observed band size: 200 kDa Exposure time: 3 minutes; 6% 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 (NBP3-33111) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: ZEB1 Antibody (JE57-64) [NBP3-33111] - Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue with Rabbit anti-ZEB1 antibody (NBP3-33111) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (NBP3-33111) at 1/200 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/nbp3-33111_rabbit-zeb1-mab-je57-64-29820241492615.jpg)
![Immunohistochemistry-Paraffin: IRF6 Antibody [NBP2-98729] - Staining of mouse IRF6 in mouse small intestine with rabbit polyclonal antibody (1:1000).](http://images.novusbio.com/fullsize/IRF6-Antibody-Immunohistochemistry-Paraffin-NBP2-98729-img0002.jpg "Immunohistochemistry-Paraffin: IRF6 Antibody [NBP2-98729] - Staining of mouse IRF6 in mouse small intestine with rabbit polyclonal antibody (1:1000).")
![Immunocytochemistry/Immunofluorescence: IRF6 Antibody [NBP2-98729] - Immunofluorescence staining of IRF6 in COS7 cells. Cells were fixed with 4% PFA, permeabilzed with 0.3% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-98729 antibody (1:1000) at 4C overnight. Then cells were stained with the Alexa Fluor(R)488-conjugated Goat Anti-rabbit IgG Secondary antibody (green).Positive staining was localized to cytoplasm and nucleus.](http://images.novusbio.com/fullsize/nbp2-98729_rabbit-polyclonal-irf6-antibody-235202521451760.png)
![Immunohistochemistry: CAMP/LL37/FALL39/Cathelicidin Antibody (PSH01-73) [NBP3-32194] - Immunofluorescence analysis of paraffin-embedded human spleen tissue labeling CAMP/LL37/FALL39/Cathelicidin with Rabbit anti-CAMP/LL37/FALL39/Cathelicidin antibody (NBP3-32194) at 1/200 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32194, 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/nbp3-32194_rabbit-camp-ll37-fall39-cathelicidin-mab-psh01-73-298202414115419.jpg "Immunohistochemistry: CAMP/LL37/FALL39/Cathelicidin Antibody (PSH01-73) [NBP3-32194] - Immunofluorescence analysis of paraffin-embedded human spleen tissue labeling CAMP/LL37/FALL39/Cathelicidin with Rabbit anti-CAMP/LL37/FALL39/Cathelicidin antibody (NBP3-32194) at 1/200 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32194, 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: CAMP/LL37/FALL39/Cathelicidin Antibody (PSH01-73) [NBP3-32194] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-CAMP/LL37/FALL39/Cathelicidin antibody (NBP3-32194) 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 (NBP3-32194) 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/nbp3-32194_rabbit-camp-ll37-fall39-cathelicidin-mab-psh01-73-298202414304194.jpg)
![Western Blot: IFIT3 Antibody [NBP3-12668] - Lane A: HeLa Whole Cell LysateLane B: A549 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:56 kDaObserved band size:58 kDa](http://images.novusbio.com/fullsize/IFIT3-Antibody-Western-Blot-NBP3-12668-img0001.jpg "Western Blot: IFIT3 Antibody [NBP3-12668] - Lane A: HeLa Whole Cell LysateLane B: A549 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:56 kDaObserved band size:58 kDa")
![Immunoprecipitation: IFIT3 Antibody [NBP3-12668] - Lane A:0.5 mg A549 Whole Cell Lysate4 uL anti-IFIT3 rabbit polyclonal antibody and 60 ug of Immunomagnetic beads Protein A/G.Primary antibody:Anti-IFIT3 rabbit polyclonal antibody,at 1:100 dilution Secondary antibody:Clean-Blot IP Detection Reagent (HRP) at 1:1000dilutionDeveloped using the ECL technique.Performed under reducing conditions.Predicted band size: 56 kDaObserved band size :58 kDa](http://images.novusbio.com/fullsize/IFIT3-Antibody-Immunoprecipitation-NBP3-12668-img0002.jpg)
![Western Blot: IFIT3 Antibody - BSA Free [NBP3-12668] - NBP3-12668 at 1:500 dilution Lane A: HeLa Whole Cell Lysate Lane B: A549 Whole Cell Lysate Lysates/proteins at 30 ug per lane. Secondary Goat Anti-Rabbit IgG (H+L)/HRP at 1/10000 dilution. Developed using the ECL technique. Performed under reducing conditions. Predicted band size:56 kDa Observed band size:58 kDa](http://images.novusbio.com/fullsize/nbp3-12668_rabbit-polyclonal-ifit3-antibody-235202511444453.png)
![Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human breast cancer with rabbit monoclonal antibody (1:300).](http://images.novusbio.com/fullsize/CD117-c-kit-Antibody-351-Immunohistochemistry-Paraffin-NBP2-90037-img0003.jpg "Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human breast cancer with rabbit monoclonal antibody (1:300).")
![Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human melanoma with rabbit monoclonal antibody (1:300).](http://images.novusbio.com/fullsize/CD117-c-kit-Antibody-351-Immunohistochemistry-Paraffin-NBP2-90037-img0001.jpg)
![Immunohistochemistry-Paraffin: CD117/c-kit Antibody (351) [NBP2-90037] - Staining of human c-KIT in human skin with rabbit monoclonal antibody (1:300).](http://images.novusbio.com/fullsize/CD117-c-kit-Antibody-351-Immunohistochemistry-Paraffin-NBP2-90037-img0002.jpg)
![Immunohistochemistry: CAMP/LL37/FALL39/Cathelicidin Antibody (PSH01-72) [NBP3-32193] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-CAMP/LL37/FALL39/Cathelicidin antibody (NBP3-32193) at 1/2,000 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 (NBP3-32193) 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/nbp3-32193_rabbit-camp-ll37-fall39-cathelicidin-mab-psh01-72-298202413585519.jpg "Immunohistochemistry: CAMP/LL37/FALL39/Cathelicidin Antibody (PSH01-72) [NBP3-32193] - Immunohistochemical analysis of paraffin-embedded human spleen tissue with Rabbit anti-CAMP/LL37/FALL39/Cathelicidin antibody (NBP3-32193) at 1/2,000 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 (NBP3-32193) 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.")
![Immunohistochemistry: CAMP/LL37/FALL39/Cathelicidin Antibody (PSH01-72) [NBP3-32193] - Immunofluorescence analysis of paraffin-embedded human spleen tissue labeling CAMP/LL37/FALL39/Cathelicidin with Rabbit anti-CAMP/LL37/FALL39/Cathelicidin antibody (NBP3-32193) at 1/50 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32193, green) at 1/50 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/nbp3-32193_rabbit-camp-ll37-fall39-cathelicidin-mab-psh01-72-29820241420956.jpg)
![Western Blot: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Western blot analysis of Clusterin/APOJ on different lysates with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: A431 cell lysate Lane 4: PANC-1 cell lysate Lane 5: MCF7 cell lysate Lane 6: T-47D cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 52 kDa Observed band size: 35-80 kDa Exposure time: 1 minute 50 seconds; ECL; 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 (NBP3-32196) 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/nbp3-32196_rabbit-clusterin-apoj-mab-psh04-33-27820241521244.jpg "Western Blot: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Western blot analysis of Clusterin/APOJ on different lysates with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/2,000 dilution. Lane 1: HeLa cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: A431 cell lysate Lane 4: PANC-1 cell lysate Lane 5: MCF7 cell lysate Lane 6: T-47D cell lysate Lysates/proteins at 20 ug/Lane. Predicted band size: 52 kDa Observed band size: 35-80 kDa Exposure time: 1 minute 50 seconds; ECL; 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 (NBP3-32196) 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: Clusterin/APOJ Antibody (PSH04-33) [NBP3-32196] - Immunohistochemical analysis of paraffin-embedded human lung cancer tissue with Rabbit anti-Clusterin/APOJ antibody (NBP3-32196) at 1/8,000 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 (NBP3-32196) at 1/8,000 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/nbp3-32196_rabbit-clusterin-apoj-mab-psh04-33-29820241492623.jpg)
![Western Blot: IRAK4 Antibody (JE41-77) [NBP3-32482] - Western blot analysis of IRAK4 on different lysates with Rabbit anti-IRAK4 antibody (NBP3-32482) at 1/1,000 dilution. Lane 1: Jurkat cell lysate Lane 2: K-562 cell lysate Lane 3: THP-1 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 52 kDa Observed band size: 52 kDa Exposure time: 22 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 (NBP3-32482) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32482_rabbit-irak4-mab-je41-77-27820241631694.jpg "Western Blot: IRAK4 Antibody (JE41-77) [NBP3-32482] - Western blot analysis of IRAK4 on different lysates with Rabbit anti-IRAK4 antibody (NBP3-32482) at 1/1,000 dilution. Lane 1: Jurkat cell lysate Lane 2: K-562 cell lysate Lane 3: THP-1 cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 52 kDa Observed band size: 52 kDa Exposure time: 22 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 (NBP3-32482) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature.")
![Immunohistochemistry: IRAK4 Antibody (JE41-77) [NBP3-32482] - Immunohistochemical analysis of paraffin-embedded human striated muscle tissue with Rabbit anti-IRAK4 antibody (NBP3-32482) at 1/1,000 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 (NBP3-32482) 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/nbp3-32482_rabbit-irak4-mab-je41-77-298202413585559.jpg)
![Flow Cytometry: Clusterin/APOJ Antibody (013) [NBP2-89884] - Analysis of Human CLU on A549 cells. Cells were treated, stained with purified anti-Human CLU, then a FITC-conjugated second step antibody. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.](http://images.novusbio.com/fullsize/Clusterin-APOJ-Antibody-013-Flow-Cytometry-NBP2-89884-img0002.jpg "<b>Biological Strategies Validation. </b>Flow Cytometry: Clusterin/APOJ Antibody (013) [NBP2-89884] - Analysis of Human CLU on A549 cells. Cells were treated, stained with purified anti-Human CLU, then a FITC-conjugated second step antibody. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells.")
![<b>Biological Strategies Validation. </b>Immunocytochemistry/Immunofluorescence: Clusterin/APOJ Antibody (013) [NBP2-89884] - Staining of Human CLU in Hela cells. Cells were fixed with 4% PFA, permeabilzed with 1% Triton X-100 in PBS, blocked with 10% serum, and incubated with NBP2-89884 antibody (1:60) at 37c 1 hour. Then cells were stained with the Alexa Fluor(R) 488-conjugated Goat Anti-rabbit IgG secondary antibody (green). Positive staining was localized to cytoplasm.](http://images.novusbio.com/fullsize/nbp2-89884_rabbit-monoclonal-clusterin-apoj-antibody-013-235202514371330.png)
![Immunohistochemistry: MHC Class I Antibody (MEM-E/07) [NB500-310] - staining of human spleen (paraffin sections) with anti-HLA-E (clone MEM-E/07).](http://images.novusbio.com/fullsize/MHC-Class-I-Antibody-MEM-E-07-Immunohistochemistry-NB500-310-img0001.jpg "Immunohistochemistry: MHC Class I Antibody (MEM-E/07) [NB500-310] - staining of human spleen (paraffin sections) with anti-HLA-E (clone MEM-E/07).")
![Immunohistochemistry-Paraffin: Proinsulin Antibody (C-PEP-01) [NB500-413] - Staining of human pancreas (paraffin-embedded sections) with anti-human to C-peptide of Proinsulin (C-PEP-01).](http://images.novusbio.com/fullsize/Proinsulin-Antibody-C-PEP-01-Immunohistochemistry-Paraffin-NB500-413-img0001.jpg "Immunohistochemistry-Paraffin: Proinsulin Antibody (C-PEP-01) [NB500-413] - Staining of human pancreas (paraffin-embedded sections) with anti-human to C-peptide of Proinsulin (C-PEP-01).")