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Cloning and identification of the H-2D super(p) gene
The authors have cloned six different class I genes from a B10.P sperm library. After cotransfection with the herpes simplex tk gene, one L-cell line was found to react with six H-2D super(p)-specific monoclonal antibodies. The cell line L12a did not react with K super(p)-specific monoclonal antibod...
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Published in: | Immunogenetics (New York) 1984-01, Vol.19 (3), p.194-204 |
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container_title | Immunogenetics (New York) |
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creator | Macchi, MJ Woodward, J G McLaughlin-Taylor, E Griffin, J Hood, L Frelinger, JA |
description | The authors have cloned six different class I genes from a B10.P sperm library. After cotransfection with the herpes simplex tk gene, one L-cell line was found to react with six H-2D super(p)-specific monoclonal antibodies. The cell line L12a did not react with K super(p)-specific monoclonal antibodies. This identification was confirmed by mapping a 2.5 kb Bam H1 restriction fragment present in the lambda 12a DNA clone to the D-TL region of H-2 super(p). Only a single 8.8 kb Bam H1 fragment can be assigned to K super(p) by restriction fragment length polymorphism, while many others map to the D-TL interval. A restriction map of lambda 12a is presented. |
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After cotransfection with the herpes simplex tk gene, one L-cell line was found to react with six H-2D super(p)-specific monoclonal antibodies. The cell line L12a did not react with K super(p)-specific monoclonal antibodies. This identification was confirmed by mapping a 2.5 kb Bam H1 restriction fragment present in the lambda 12a DNA clone to the D-TL region of H-2 super(p). Only a single 8.8 kb Bam H1 fragment can be assigned to K super(p) by restriction fragment length polymorphism, while many others map to the D-TL interval. 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title | Cloning and identification of the H-2D super(p) gene |
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