Projects per year
Abstract
Since connexin expression is partly regulated at the protein level, immunoblot analysis represents a frequently addressed technique in the connexin research field. The present chapter describes the set-up of an immunoblot procedure, including protein extraction and quantification from biological samples, gel electrophoresis, protein transfer and immunoblotting, which is optimized for analysis of connexins in liver tissue. In essence, proteins are separated on a polyacrylamide gel using sodiumdodecylsulfate followed by transfer of proteins on a nitrocellulose membrane. The latter allows specific detection of connexins with antibodies combined with revelation through enhanced chemiluminescence.
Original language | English |
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Title of host publication | Gap Junction Protocols |
Editors | Mathieu Vinken, Scott Johnstone |
Place of Publication | New York |
Publisher | Springer Protocols |
Pages | 37-53 |
ISBN (Print) | 978-1-4939-3664-9 |
Publication status | Published - 22 May 2016 |
Keywords
- connexin
- protein extraction
- sodiumdodecylsulfate polyacrylamide gel electrophoresis
- immunoblot analysis
- antibody
- enhanced chemiluminescence
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OZR2651: International Joint Research Group - Liver Connexin and Pannexin Research Group (LCPR)
Vinken, M., Rogiers, V., Cogliati, B. & Dagli, M. L.
1/08/14 → 1/07/26
Project: Fundamental
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EU457: CONNECT: Connexin and pannexin channels as drug targets and biomarkers in acute and chronic liver disease
1/03/14 → 28/02/19
Project: Fundamental
Activities
- 1 Talk or presentation at a workshop/seminar
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The role of connexins, pannexins and their channels in liver fibrosis
Sara Crespo Yanguas (Speaker)
28 Nov 2018Activity: Talk or presentation › Talk or presentation at a workshop/seminar