| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-43348-0.5mg | |||
| BSA Free | NBP1-43348-0.05mg | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-22596-50ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-88079-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP1-88753-25ul | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| Azide and BSA Free | NBP2-70172 | |||
| Formulation | Catalog # | Availability | Price | |
|---|---|---|---|---|
| BSA Free | NBP3-38124-20ul | |||
![Flow Cytometry: VE-Cadherin Antibody (BV13) [NBP1-43348] - Analysis using the Biotin conjugate of NBP1-43348. Staining of bEnd.3 cell line with 0.5 micrograms of Rat IgG1 k Isotype Control Biotin (blue histogram) or 0.125 micrograms of Anti-Mouse CD144 (VE-Cadherin) Biotin purple histogram) followed by Streptavidin PE. Total viable cells were used for analysis.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-BV13-Flow-Cytometry-NBP1-43348-img0003.jpg "Flow Cytometry: VE-Cadherin Antibody (BV13) [NBP1-43348] - Analysis using the Biotin conjugate of NBP1-43348. Staining of bEnd.3 cell line with 0.5 micrograms of Rat IgG1 k Isotype Control Biotin (blue histogram) or 0.125 micrograms of Anti-Mouse CD144 (VE-Cadherin) Biotin purple histogram) followed by Streptavidin PE. Total viable cells were used for analysis.")
![Flow Cytometry: VE-Cadherin Antibody (BV13) [NBP1-43348] - Staining of bEnd.3 cell line with 0.5 ug of Rat IgG1 K Isotype Control Purified (open histogram) or 0.5 ug of AntiMouse CD144 (VE-Cadherin) Purified (filled histogram) followed by F(ab')2 Anti-Rat IgG PE. Total viable cells were used for analysis.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-BV13-Flow-Cytometry-NBP1-43348-img0001.jpg)
![Western Blot: RNASET2 Antibody [NBP2-81890] - Analysis of RNASET2 in SW480 cell lysate with RNASET2 antibody at 1 ug/ml in (A) the absence and (B) the presence of blocking peptide.](http://images.novusbio.com/fullsize/RNASET2-Antibody-Western-Blot-NBP2-81890-img0001.jpg "Western Blot: RNASET2 Antibody [NBP2-81890] - Analysis of RNASET2 in SW480 cell lysate with RNASET2 antibody at 1 ug/ml in (A) the absence and (B) the presence of blocking peptide.")
![Immunohistochemistry: RNASET2 Antibody - BSA Free [NBP2-81890] - Immunocytochemistry of RNASET2 in SW480 cells with RNASET2 antibody at 2.5 u/ml.](http://images.novusbio.com/fullsize/nbp2-81890_rabbit-polyclonal-rnaset2-antibody-2711202420115521.jpg)
![Immunocytochemistry/ Immunofluorescence: RNASET2 Antibody - BSA Free [NBP2-81890] - Immunofluorescence of RNASET2 in SW480 cells with RNASET2 antibody at 5 ug/ml.](http://images.novusbio.com/fullsize/nbp2-81890_rabbit-polyclonal-rnaset2-antibody-2711202419293824.jpg)
![Western Blot: CLIC4 Antibody (JE65-09) [NBP3-32192] - Western blot analysis of CLIC4 on different lysates with Rabbit anti-CLIC4 antibody (NBP3-32192) at 1/1,000 dilution. Lane 1: HeLa cell lysate (20 ug/Lane) Lane 2: JAR cell lysate (20 ug/Lane) Lane 3: HepG2 cell lysate (20 ug/Lane) Lane 4: RAW264.7 cell lysate (20 ug/Lane) Lane 5: Neuro-2a cell lysate (20 ug/Lane) Lane 6: C6 cell lysate (20 ug/Lane) Lane 7: Human kidney tissue lysate (40 ug/Lane) Lane 8: Rat kidney tissue lysate (40 ug/Lane) Predicted band size: 29 kDa Observed band size: 29 kDa Exposure time: 24 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 (NBP3-32192) at 1/1,000 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/nbp3-32192_rabbit-clic4-mab-je65-09-278202416285255.jpg "Western Blot: CLIC4 Antibody (JE65-09) [NBP3-32192] - Western blot analysis of CLIC4 on different lysates with Rabbit anti-CLIC4 antibody (NBP3-32192) at 1/1,000 dilution. Lane 1: HeLa cell lysate (20 ug/Lane) Lane 2: JAR cell lysate (20 ug/Lane) Lane 3: HepG2 cell lysate (20 ug/Lane) Lane 4: RAW264.7 cell lysate (20 ug/Lane) Lane 5: Neuro-2a cell lysate (20 ug/Lane) Lane 6: C6 cell lysate (20 ug/Lane) Lane 7: Human kidney tissue lysate (40 ug/Lane) Lane 8: Rat kidney tissue lysate (40 ug/Lane) Predicted band size: 29 kDa Observed band size: 29 kDa Exposure time: 24 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 (NBP3-32192) at 1/1,000 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.")
![Immunocytochemistry/ Immunofluorescence: CLIC4 Antibody (JE65-09) [NBP3-32192] - Immunocytochemistry analysis of HeLa cells labeling CLIC4 with Rabbit anti-CLIC4 antibody (NBP3-32192) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS 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-CLIC4 antibody (NBP3-32192) at 1/200 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.](http://images.novusbio.com/fullsize/nbp3-32192_rabbit-clic4-mab-je65-09-2920241114835.jpg)
![Flow Cytometry: CLIC4 Antibody (JE65-09) [NBP3-32192] - Flow cytometric analysis of HeLa cells labeling CLIC4. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32192, 1/100) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32192_rabbit-clic4-mab-je65-09-29202416372180.jpg)
![Western Blot: CLIC4 Antibody (SR1481) [NBP3-22596] - Western blot analysis using NBP3-22596 in 293 cell lysate.](http://images.novusbio.com/fullsize/nbp3-22596_rabbit-clic4-mab-sr1481-672023106272.jpg "Western Blot: CLIC4 Antibody (SR1481) [NBP3-22596] - Western blot analysis using NBP3-22596 in 293 cell lysate.")
![Western Blot: RNASET2 Antibody [NBP1-88753] - Analysis in control (vector only transfected HEK293T lysate) and RNASET2 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).](http://images.novusbio.com/fullsize/RNASET2-Antibody-Western-Blot-NBP1-88753-img0006.jpg "Western Blot: RNASET2 Antibody [NBP1-88753] - Analysis in control (vector only transfected HEK293T lysate) and RNASET2 over-expression lysate (Co-expressed with a C-terminal myc-DDK tag (3.1 kDa) in mammalian HEK293T cells).")
![Immunohistochemistry-Paraffin: RNASET2 Antibody [NBP1-88753] - Staining of human corpus, uterine shows strong cytoplasmic positivity in glandular cells.](http://images.novusbio.com/fullsize/RNASET2-Antibody-Immunohistochemistry-Paraffin-NBP1-88753-img0002.jpg)
![Western Blot: RNASET2 Antibody [NBP1-88753] - Analysis in human cell line THP-1.](http://images.novusbio.com/fullsize/RNASET2-Antibody-Western-Blot-NBP1-88753-img0005.jpg)
![Western Blot: Angiopoietin-1 Antibody (8H2) [NBP2-46519] - Human recombinant protein fragment corresponding to amino acids 198-498 of human ANGPT1 (NP_001137) produced in E.coli.](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-8H2-Western-Blot-NBP2-46519-img0002.jpg "Western Blot: Angiopoietin-1 Antibody (8H2) [NBP2-46519] - Human recombinant protein fragment corresponding to amino acids 198-498 of human ANGPT1 (NP_001137) produced in E.coli.")
![Immunohistochemistry: Angiopoietin-1 Antibody (8H2) [NBP2-46519] - Analysis of Carcinoma of Human liver tissue.(Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-8H2-Immunohistochemistry-NBP2-46519-img0001.jpg)
![Western Blot: VE-Cadherin Antibody (16B1) [NBP2-00342] - EDTA-passaged (left) and Trypsin-passaged (right) Human Umbilical Vein Endothelial Cells (HUVEC) were resolved by SDS -PAGE and immunoblotted with 2 ug/mL of Anti-Human CD144 (VE-Cadherin) Purified and revealed with Anti-Rat IgG HRP.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-16B1-Western-Blot-NBP2-00342-img0002.jpg "Western Blot: VE-Cadherin Antibody (16B1) [NBP2-00342] - EDTA-passaged (left) and Trypsin-passaged (right) Human Umbilical Vein Endothelial Cells (HUVEC) were resolved by SDS -PAGE and immunoblotted with 2 ug/mL of Anti-Human CD144 (VE-Cadherin) Purified and revealed with Anti-Rat IgG HRP.")
![Flow Cytometry: VE-Cadherin Antibody (16B1) [NBP2-00342] - Analysis using the Biotin conjugate of NBP2-00342. Staining of Human Umbilical Vein Endothelial Cells (HUVEC) with 0.25 ug of Mouse IgG1 kappa Isotype Control Biotin (open histogram) or 0.125 ug of Anti-Human CD144 (VE-Cadherin) Biotin (filled histogram)](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-16B1-Flow-Cytometry-NBP2-00342-img0007.jpg)
![Flow Cytometry: VE-Cadherin Antibody (16B1) [NBP2-00342] - Analysis using the Allophycocyanin conjugate of NBP2-00342. Staining of Human Umbilical Vein Endothelial Cells.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-16B1-Flow-Cytometry-NBP2-00342-img0006.jpg)
![Flow Cytometry: VE-Cadherin Antibody (16B1) [NBP2-00342] - Analysis using the PE conjugate of NBP2-00342.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-16B1-Flow-Cytometry-NBP2-00342-img0008.jpg)
![Western Blot: Angiopoietin-1 Antibody (6C4S7) [NBP3-16269] - Western blot analysis of extracts of various cell lines, using Angiopoietin-1 Rabbit mAb (NBP3-16269) 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 Enhanced Kit. Exposure time: 3min.](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-6C4S7-Western-Blot-NBP3-16269-img0002.jpg "Western Blot: Angiopoietin-1 Antibody (6C4S7) [NBP3-16269] - Western blot analysis of extracts of various cell lines, using Angiopoietin-1 Rabbit mAb (NBP3-16269) 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 Enhanced Kit. Exposure time: 3min.")
![Immunohistochemistry-Paraffin: Angiopoietin-1 Antibody (6C4S7) [NBP3-16269] - Immunohistochemistry of paraffin-embedded human colon using Angiopoietin-1 Rabbit mAb (NBP3-16269) at dilution of 1:100 (40x lens).Perform microwave antigen retrieval with 10 mM PBS buffer pH 7.2 before commencing with IHC staining protocol.](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-6C4S7-Immunohistochemistry-Paraffin-NBP3-16269-img0001.jpg)
![Western Blot: NEDD1 Antibody [NBP3-38124] - Western blot analysis of various lysates using NEDD1 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated 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/nbp3-38124_rabbit-nedd1-pab-1012202411592826.jpg "Western Blot: NEDD1 Antibody [NBP3-38124] - Western blot analysis of various lysates using NEDD1 Rabbit pAb at 1:1000 dilution.Secondary antibody: HRP-conjugated 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.")
![Immunocytochemistry/ Immunofluorescence: NEDD1 Antibody [NBP3-38124] - Immunofluorescence analysis of L929 cells using NEDD1 Rabbit pAb at dilution of 1:100. Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.](http://images.novusbio.com/fullsize/nbp3-38124_rabbit-nedd1-pab-1012202411535851.jpg)
![Western Blot: Angiopoietin-1 Antibody (OTI8H2) - Azide and BSA Free [NBP2-70172] - Human recombinant protein fragment corresponding to amino acids 198-498 of human ANGPT1 (NP_001137) produced in E.coli.](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-OTI8H2-Azide-and-BSA-Free-Western-Blot-NBP2-70172-img0001.jpg "Western Blot: Angiopoietin-1 Antibody (OTI8H2) - Azide and BSA Free [NBP2-70172] - Human recombinant protein fragment corresponding to amino acids 198-498 of human ANGPT1 (NP_001137) produced in E.coli.")
![Immunohistochemistry: Angiopoietin-1 Antibody (OTI8H2) - Azide and BSA Free [NBP2-70172] - Analysis of Carcinoma of Human liver tissue.(Heat-induced epitope retrieval by 1 mM EDTA in 10mM Tris, pH8.5, 120C for 3min)](http://images.novusbio.com/fullsize/Angiopoietin-1-Antibody-OTI8H2-Azide-and-BSA-Free-Immunohistochemistry-NBP2-70172-img0002.jpg)
![Western Blot: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Western blot analysis of VE-Cadherin on different lysates with Rabbit anti-VE-Cadherin antibody (NBP3-33088) at 1/2,000 dilution. Lane 1: EA.hy926-si NT cell lysate Lane 2: EA.hy926-si VE Cadherin cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 88 kDa Observed band size: 140 kDa Exposure time: 1 minute 2 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 (NBP3-33088) 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/nbp3-33088_rabbit-ve-cadherin-mab-psh03-15-288202414191513.jpg "Western Blot: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Western blot analysis of VE-Cadherin on different lysates with Rabbit anti-VE-Cadherin antibody (NBP3-33088) at 1/2,000 dilution. Lane 1: EA.hy926-si NT cell lysate Lane 2: EA.hy926-si VE Cadherin cell lysate Lysates/proteins at 10 ug/Lane. Predicted band size: 88 kDa Observed band size: 140 kDa Exposure time: 1 minute 2 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 (NBP3-33088) 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.")
![Immunocytochemistry/ Immunofluorescence: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Immunocytochemistry analysis of HeLa cells labeling VE-Cadherin with Rabbit anti-VE-Cadherin antibody (NBP3-33088) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS 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-VE-Cadherin antibody (NBP3-33088) 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. 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/nbp3-33088_rabbit-ve-cadherin-mab-psh03-15-29202410234272.jpg)
![Flow Cytometry: VE-Cadherin Antibody (PSH03-15) [NBP3-33088] - Flow cytometric analysis of EA.hy926 cells labeling VE-Cadherin. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (NBP3-33088, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-33088_rabbit-ve-cadherin-mab-psh03-15-2920241645321.jpg)