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Simplified Gene-Fragment Phage Display System for Epitope Mapping

We describe a simple and efficient system for epitope mapping by cloning random gene fragments into a specially designed gIIIp-based phage display vector. DNA encoding the antigen of interest is PCR-amplified and partially digested with DNaseI to generate 50–150-bp-long fragments, which are polished...

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Bibliografiske detaljer
Principais autores: S. Gupta, K. Arora, A. Sampath, S. Khurana, S.S. Singh, A. Gupta, V.K. Chaudhary
Format: Artigo
Sprog:Inglês
Udgivet: Taylor & Francis Group 1999-08-01
Serier:BioTechniques
Online adgang:https://www.future-science.com/doi/10.2144/99272st04
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