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Table 4 Oligonucleotides used in this study

From: CRISPR/Cas9 Knockout Strategies to Ablate CCAT1 lncRNA Gene in Cancer Cells

Gene

Sequence (5′ to 3′)

Product (bP)

Application

CCAT1 (NR_108049.1)

F: CTGACAACATCGACTTTG

R: CTCACAGTTTTCAAGGGA

Probe: FAM-CTTAGCCATACAGAGCCAACCTG-BHQ1

108

qPCR

F: CGATCGttctgttttcaatggggatt

R: TCGAGggagctgcggataacagcatat

546

Cloning of left homology arm

F: CTAGTCCCgcatcacagctactgtcaaccc

R: ATCCCCtcaaagcacttctgtggtagga

832

Cloning of right homology arm

Forward-1: CACATGGCTCCCATCACACTA

Reverse-1: GGGGGAAGAAATTTAAGATGCACA

1298 (w.t.) 409 (ko)

PCR confirmation of CRISPR Excision knockout allele

Forward-2: CACGCAGATCACATGACCCT

Reverse-2: CGGGCCATTTACCGTAAG

1627 (ko)

PCR confirmation of CRISPR HDR knockout allele

Forward-2: CACGCAGATCACATGACCCT

R: AAACgatggagctgcggataacagC

843 (w.t.)

PCR confirmation of CRISPR HDR wild-type allele

Forward-3: CGGGCCATTTACCGTAAG

Reverse-1: GGGGGAAGAAATTTAAGATGCACA

495 (ko)

PCR confirmation of CRISPR du-HITI knockout allele

F: CACCGaatcggagtccaaagccatt

R: AAACaatggctttggactccgattC

sgRNA (downstream of Exon 1)

F: CACCGataatggaggggatttacgt

R: AAACacgtaaatcccctccattatC

sgRNA (upstream of Exon 1)

F: CACCGctgttatccgcagctccatc

R: AAACgatggagctgcggataacagC

sgRNA (Exon 2)

F: CACCGaatggctttggactccgatttgg

R: AAACccaaatcggagtccaaagccattC

sgRNA bait (+PAM) (downstream of Exon 1)

b-Actin

F: TGCAGAAGGAGATCACTG

R: CTTGCTGATCCACATCTG

Probe: CY5-AAGATCAAGATCATTGCTCCTCCTGA-BHQ2

141

qPCR