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. 2005 Oct;4(10):1712–1724. doi: 10.1128/EC.4.10.1712-1724.2005

TABLE 2.

Oligonucleotide primers used in this study

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
a

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′.