Sequence analysis of cloned cDNA encoding part of an immunoglobulin heavy chain (original) (raw)
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Molecular Biology Institute and Department of Biology, University of California
Los Angeles, CA 90024, USA
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Molecular Biology Institute and Department of Biology, University of California
Los Angeles, CA 90024, USA
Search for other works by this author on:
Molecular Biology Institute and Department of Biology, University of California
Los Angeles, CA 90024, USA
Search for other works by this author on:
Cite
John Rogers, Patrick Clarke, Winston Salser, Sequence analysis of cloned cDNA encoding part of an immunoglobulin heavy chain, Nucleic Acids Research, Volume 6, Issue 10, 25 July 1979, Pages 3305–3322, https://doi.org/10.1093/nar/6.10.3305
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Abstract
The recombinant plasmid pH21-1 consists of mouse-derived complementary DNA (cDNA) in the E. coli plasmid pMB9. The mouse insertion has been completely sequenced, and encodes the CH3 domain and half the CH2 domain of the immunoglobulin γ1 heavy chain. The predicted amino acid sequence differs at several positions from that previously published for this protein. The pattern of codon usage resembles that in some other eukaryotic messenger RNAs. A computer program has been used to predict the optimum secondary structure for the mRNA encoding the CH3 domain and the inter-domain junction.
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