VE-Cadherin Antibodies
We offer VE-Cadherin Antibodies for use in common research applications: ELISA, Flow Cytometry, Functional, Immunoassay, Immunocytochemistry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Frozen, Immunohistochemistry-Paraffin, Immunoprecipitation, Western Blot. Each VE-Cadherin Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our VE-Cadherin Antibodies can be used in a variety of model species: Human, Mouse, Rat. Use the list below to choose the VE-Cadherin Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our VE-Cadherin polyclonal antibodies and browse our VE-Cadherin monoclonal antibody catalog.
Alternate Names for VE-Cadherin Antibodies
anti-VE-Cadherin antibody, anti-CDH5 antibody, anti-7B4 antibody, anti-7B4 antigen antibody, anti-cadherin 5, type 2 (vascular endothelium) antibody, anti-cadherin 5, type 2, VE-cadherin (vascular epithelium) antibody, anti-cadherin-5 antibody, anti-CD144 antibody, anti-CD144 antigen antibody, anti-endothelial-specific cadherin antibody, anti-FLJ17376 antibody, anti-Vascular endothelial cadherin antibody
25 Results for "ve-cadherin" in Primary Antibodies
![Immunocytochemistry/Immunofluorescence: VE Cadherin Antibody (BV9) [NB600-1409] - Endothelial cells were fixed with 4% PAF (15 min, room temp), and then permeabilized with 0.5% TritionX-100 (3 min, room temperature). Cells were incubated with a final concentration of 10mg/ml BV9. Secondary detection was performed with anti-mouse Alexa-Fluor 647 and counterstained using DAPI.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-BV9-Immunocytochemistry-Immunofluorescence-NB600-1409-img0008.jpg "Immunocytochemistry/Immunofluorescence: VE Cadherin Antibody (BV9) [NB600-1409] - Endothelial cells were fixed with 4% PAF (15 min, room temp), and then permeabilized with 0.5% TritionX-100 (3 min, room temperature). Cells were incubated with a final concentration of 10mg/ml BV9. Secondary detection was performed with anti-mouse Alexa-Fluor 647 and counterstained using DAPI.")
![Flow Cytometry: VE Cadherin Antibody (BV9) [NB600-1409] - HUVEC cells were stained with antibody BV9 in PBS/0.1% saponin for 1h at 4 degrees C.(Black- no stain, Red- isotype control, Blue-HM2032-BV9)](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-BV9-Flow-Cytometry-NB600-1409-img0007.jpg)
![Western Blot: VE-Cadherin Antibody (BV14) [NBP1-43347] - Non-reduced (left) and reduced (right) bEnd.3 cell line lysates were loaded at 1x10^5 cells/lane, probed with 2 ug/mL of Anti-Mouse CD144 (VE-Cadherin) Purified and revealed with Anti-Rat IgG HRP.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-BV14-Western-Blot-NBP1-43347-img0003.jpg "Western Blot: VE-Cadherin Antibody (BV14) [NBP1-43347] - Non-reduced (left) and reduced (right) bEnd.3 cell line lysates were loaded at 1x10^5 cells/lane, probed with 2 ug/mL of Anti-Mouse CD144 (VE-Cadherin) Purified and revealed with Anti-Rat IgG HRP.")
![Western Blot: VE-Cadherin Antibody (3D5C7) [NBP2-37420] - Western blot analysis using CDH5 mouse mAb against MCF-7 (1), A549 (2), HUVE-12 (3) cell lysate, and rat lung (4) tissue lysate.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-3D5C7-Western-Blot-NBP2-37420-img0003.jpg "Western Blot: VE-Cadherin Antibody (3D5C7) [NBP2-37420] - Western blot analysis using CDH5 mouse mAb against MCF-7 (1), A549 (2), HUVE-12 (3) cell lysate, and rat lung (4) tissue lysate.")
![Flow Cytometry: VE-Cadherin Antibody (3D5C7) [NBP2-37420] - Flow cytometric analysis of Jurkat cells using CDH5 mouse mAb (green) and negative control (purple).](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-3D5C7-Flow-Cytometry-NBP2-37420-img0004.jpg)
![Western Blot: VE-Cadherin Antibody (3D5C7) [NBP2-37420] - Western blot analysis using CDH5 mAb against human CDH5 recombinant protein. (Expected MW is 47.6 kDa)](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-3D5C7-Western-Blot-NBP2-37420-img0002.jpg)
![ELISA: VE-Cadherin Antibody (3D5C7) [NBP2-37420] - Red: Control Antigen (100ng); Purple: Antigen (10ng); Green: Antigen (50ng); Blue: Antigen (100ng);](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-3D5C7-ELISA-NBP2-37420-img0001.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.](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: VE-Cadherin Antibody (MM0012-8A03) - Azide and BSA Free [NB110-60978] - Lysates of HUVECs with Mouse anti-Human VE-Cadherin (MM0012-8A03) antibody.](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-MM0012-8A03-Azide-and-BSA-Free-Western-Blot-NB110-60978-img0003.jpg "Western Blot: VE-Cadherin Antibody (MM0012-8A03) - Azide and BSA Free [NB110-60978] - Lysates of HUVECs with Mouse anti-Human VE-Cadherin (MM0012-8A03) antibody.")
![Immunohistochemistry-Paraffin: VE-Cadherin Antibody (MM0012-8A03) [NB110-60978] - Formalin fixed and paraffin embedded human placental tissue section is subjected to IHC with anti human VE-Cadherin](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-MM0012-8A03-Immunohistochemistry-Paraffin-NB110-60978-img0002.jpg)
![Immunohistochemistry-Paraffin: VE-Cadherin Antibody (MM0012-8A03) [NB110-60978] - Formalin fixed and paraffin embedded human placental tissue section is subjected to IHC with anti human VE-Cadherin](http://images.novusbio.com/fullsize/VE-Cadherin-Antibody-MM0012-8A03-Immunohistochemistry-Paraffin-NB110-60978-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: 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)