Author: Rogers, J.; Schoepp, R.J.; Schröder, O.; Clements, T.L.; Holland, T.F.; Li, J.Q.; Li, J.; Lewis, L.M.; Dirmeier, R.P.; Frey, G.J.; Tan, X.; Wong, K.; Woodnutt, G.; Keller, M.; Reed, D.S.; Kimmel, B.E.; Tozer, E.C.
Title: Rapid discovery and optimization of therapeutic antibodies against emerging infectious diseases Document date: 2008_5_13
ID: xkx56h0o_41
Snippet: Two libraries were constructed from the spleens of three mice immunized with SARS-CoV. These libraries had a complexity of 30 000 and 300 000 members and were generated by reverse transcription polymerase chain reaction using antibody-specific primers. The smaller library was generated for proof of principle studies and the larger was subsequently made to increase the screening population......
Document: Two libraries were constructed from the spleens of three mice immunized with SARS-CoV. These libraries had a complexity of 30 000 and 300 000 members and were generated by reverse transcription polymerase chain reaction using antibody-specific primers. The smaller library was generated for proof of principle studies and the larger was subsequently made to increase the screening population.
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