TEV Protease Antibodies
We offer TEV Protease Antibodies for use in common research applications: ELISA, Western Blot. Each TEV Protease Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our TEV Protease Antibodies can be used in a variety of model species: Virus. Use the list below to choose the TEV Protease 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 TEV Protease polyclonal antibodies and browse our TEV Protease monoclonal antibody catalog.
Alternate Names for TEV Protease Antibodies
anti-TEV Protease antibody
2 Results for "tev-protease" in Primary Antibodies
![Western Blot: TEV Protease Antibody [NBP1-97669] - E.coli lysate containing recombinant TEV protease, NBP1-97669 used at 1:1000 dilution.](http://images.novusbio.com/fullsize2/TEV Protease Antibody-Western Blot-NBP1-97669-img0001.jpg "Western Blot: TEV Protease Antibody [NBP1-97669] - E.coli lysate containing recombinant TEV protease, NBP1-97669 used at 1:1000 dilution.")
![Western Blot: TEV Protease Antibody (9A10-4C3) [NBP2-29909] - Analysis of TEV cleavage site was performed by loading the indicated amounts of TEV control protein and 5ul of Lane Marker Reducing Sample Buffer per well onto a 4-20% Tris-HCl polyacrylamide gel. Proteins were transferred to a PVDF membrane and blocked with 5% BSA/TBST for at least 1 hour. The membrane was probed with a TEV cleavage site monoclonal antibody at a dilution of 1:1000 overnight at 4C on a rocking platform, washed in TBS-0.1%Tween 20, and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:15,000 for at least 1 hour. Chemiluminescent detection was performed using SuperSignal West Dura.](http://images.novusbio.com/fullsize2/TEV Protease Antibody (9A10-4C3)-Western Blot-NBP2-29909-img0003.jpg "Western Blot: TEV Protease Antibody (9A10-4C3) [NBP2-29909] - Analysis of TEV cleavage site was performed by loading the indicated amounts of TEV control protein and 5ul of Lane Marker Reducing Sample Buffer per well onto a 4-20% Tris-HCl polyacrylamide gel. Proteins were transferred to a PVDF membrane and blocked with 5% BSA/TBST for at least 1 hour. The membrane was probed with a TEV cleavage site monoclonal antibody at a dilution of 1:1000 overnight at 4C on a rocking platform, washed in TBS-0.1%Tween 20, and probed with a goat anti-mouse IgG-HRP secondary antibody at a dilution of 1:15,000 for at least 1 hour. Chemiluminescent detection was performed using SuperSignal West Dura.")