TABLE 2.
Primer | Sequencea |
---|---|
392 XFP | GAGTGCCATGCCCGAAGGTTATG |
599 U3 | GGAGTTGGATTAGATGATAAAGGTGATGG |
600 U2 | GTGTTACGAATCAATGGCACTACAGC |
601 H2 | CAACGAAATGGCCTCCCCTACCACAG |
602 H3 | GGACGAATTGAAGAAAGCTGGTGCAACCG |
797 S1-BNI1 | ATCACAAACATCTTTTCATCATCCACTACTATCACCAGTGCTAGTGCAGTTTCAATTAATTACCATATTCTTCAACCTCATCCTCCCTTACCTCCTCCCTgaagcttcgtacgctgcaggtc |
798 S2-BNI1 | CTTAACTTGTAAACTCACATGGTATATAATATGTAAATACAACTTTGTACAGATATAAAAATTAATAGCTATATTTCATTTAAATACATATACAAAAAAAAtctgatatcatcgatgaattcgag |
799 G1-BNI1 | CTCTCTGAGGGAGACAACGC |
800 G4-BNI1 | CAGGTTTCCAAATTGAATCGTCC |
801 G4-BNI1-MAL2p | GCACCCTTGTCGTATGGAC |
802 G1-BNI1-FP | CCGCCTGAAGGATGCTG |
804 S2-BNI1-MAL2p | GAGTTGAGTTCTGACTTGCTGATGATAATATACTAGCTGAGTCATTGGAAGACATGTCGGACACACTGTCGGTGTTGTGCTTGTCT TTATGTCGTCTCCTcattgtagttgattattagttaaaccac |
805 S1-BNR1 | GTTGTTTTTTTTTTTCAAACGCGACTTCTAAATCTCTAGCCAT ACCCGATCCAGAAACACTTGTTTTAAATTTTTTTGGTTACCACACACACAAAAATATTCgaagcttcgtacgctgcaggtc |
806 S2-BNR1 | AGAAAGTGAAAAAAAAGAAAAAAGAAAAAAAAAAAATAGTTGTTCTTTTTTAAGGAAGAGCATCACAAAATTTTTTAGACGTGTAT ATGCAGTATCGGTGTAGtctgatatcatcgatgaattcgag |
811 G1-BNR1 | GTAAGCACCGAGTCTTGTCGC |
812 G4-BNR1 | GGAAATTTCTACTCAACGAGCG |
1088 I1-BNI1 | GGAAATCAAGAACCAGAGCCTTG |
1089 I2-BNI1 | CTCTTGGCAAAGCCGGCAACAC |
1090 I1-BNR1 | GAGATAGATTCCAGGAACACGAG |
1091 I2-BNR1 | CACCAATGCCTTGACGACGTACAC |
1203 CaBNI1 | CGCGGATCCGCGGGCTCACCAACTAATGTCTCACC |
1204 CaBNI1 | TGCTCTAGAGCACGACTCTATTTATGATGACGAAGATGAAG |
1242 ADE2-down | GGTCGTATGATTGTTGAAGCAGCAC |
1243 ADE2-up | CCAGAGTTGTGAGGTCTTGGTGC |
1244 RAS1-down | GGAAAGACAAGTTAGTTATCAAGATGG |
1268 S1-BNI1-GFP | GTTCAAATAGATCTTGATGAAGTGGCTAAGAATAACAATAGTGAGggtgctggcgcaggtgcttc |
1269 S2-BNI1-GFP | CTCGAATTCATCGATGATATCAGAGGCCTGCTAAGGAGAAGCACTtttttttgtatatgtatttaaatg |
Uppercase sequences correspond to C. albicans genomic DNA. Lowercase sequences correspond to 3′-terminal annealing regions for the amplification of transformation cassettes. Bold letters indicate restriction sites used for cloning. All sequences are written from 5′ to 3′.