Table 1 of Gross, Mol Vis 2000; 6:40-50.


Table 1. Mutagenesis primers

Primers listed are designated U for upper strand. The sequence for the mutant amino acid is in red. Primers for the lower strand are the reverse complements of the corresponding upper strand primers. Both an upper and lower strand primer must be used for each PCR reaction.


                           Amino acid
Mutant    Primer    Size    Changed         Primer sequence (5' to 3')
------   --------   ----   ----------   ----------------------------------
   1     R1TSP1U    28 b     V116N      GCGGGTGGACAGCAACCCGGGCCAGGAG
   2     R1TSP2U    32 b     L147A      CGCCTTAGTGCTGGATGCCCGGCACTGCACAG
   3     R1TSP3U    34 b     R148D      CTTAGTGCTGGATCTCGATCACTGCACAGGAGGC
   4     R1TSP4U    30 b     G152A      CCGGCACTGCACAGCGGGCCAGGTCTCTGG
   5     R1TSP5U    27 b     G153A      CACTGCACAGGAGCCCAGGTCTCTGGC
   6     R1TSP6U    28 b     L208A      GGATGTGGTGGTCGCCACCAGCAGCCAG
   7     R1TSP7U    28 b     E218A      CAGGGGCGTGGCCGCGGACATCGCGCAC
   8     R1TSP8U    27 b     T237A      GTGGGCGAGCGGGCGGGGGGAGGGGCC
   9     R1TSP9U    29 b     G239T      CGAGCGGACTGGGACCGGGGCCGTGGACC
  10     R1TSP10U   28 b     I249A      CCGGAAGCTGAGGGCGGGCGAGTCTGAC
  11     R1TSP11U   34 b     E251A      GAAGCTGAGGATAGGCGCGTCTGACTTCTTCTTC
  12     R1TSP12U   29 b     G278A      GTGGGAGGGCAGCGCGGTGCTGCCCTGTG
  13     R1TSP13U   28 b     P281A      GCAGCGGGGTGCTGGCCTGTGTGGGGAC

Gross, Mol Vis 2000; 6:40-50 <http://www.molvis.org/molvis/v6/a7/>
©2000 Molecular Vision <http://www.molvis.org/molvis/>
ISSN 1090-0535