RNA-seq of 0 minute cold plasma treated Candida albicans ATCC 14053

SRX18376639 CAT0a RNA-seq of 0 minute cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862750 CAT0a CAT0a RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376640 CAT0b RNA-seq of 0 minute cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862751 CAT0b CAT0b RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376641 CAT5b RNA-seq of 5 minutes cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862752 CAT5b CAT5b RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376642 CAT5c RNA-seq of 5 minutes cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862753 CAT5c CAT5c RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376643 CAT0c RNA-seq of 0 minute cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862754 CAT0c CAT0c RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376644 CAT1a RNA-seq of 1 minute cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862755 CAT1a CAT1a RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376645 CAT1b RNA-seq of 1 minute cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862756 CAT1b CAT1b RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376646 CAT1c RNA-seq of 1 minute cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862757 CAT1c CAT1c RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376647 CAT3a RNA-seq of 3 minutes cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862758 CAT3a CAT3a RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376648 CAT3b RNA-seq of 3 minutes cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862759 CAT3b CAT3b RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376649 CAT3c RNA-seq of 3 minutes cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862760 CAT3c CAT3c RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000 SRX18376650 CAT5a RNA-seq of 5 minutes cold plasma treated Candida albicans ATCC 14053 SRP409731 bp0 The harvested cells from the treatment were mechanical lysed with bead-beating method in a Qiagen Tissuelyser II. Then, the cell lysate was subjected to total RNA extraction using Zymo Research Quick-RNA Fungal/Bacterial MiniPrep Kit and DNA was removed using DNase I. An Illumina TruSeq Stranded mRNA (with poly A selection) were used for library preparation. The prepared library was quality checked via a TapeStation 2200. RNA-seq was conducted at PE150 mode in NovaSeq 6000. SRS15862761 CAT5a CAT5a RNA-Seq TRANSCRIPTOMIC RANDOM Illumina NovaSeq 6000