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. 2018 May 30;22(9):4106–4116. doi: 10.1111/jcmm.13687

Table 1.

Primers used for PCR amplification and gene knockout

Gene Primers Sequences (5′‐3′) Size, bp
Dnmt3a 3 + 4 D3a‐Ex1seq‐L GACCACAAGAATTCCGGCTC 493
D3a‐Ex1seq‐R CGTGTGTGAATCTGTGTGGG
sgRNA1 D3a‐Ex1‐98rev ATCATCCTCCCGCTCCAAAGTGG
sgRNA2 D3a‐Ex1‐308fw TTTGAGGGGTCATCCTTGCAGGG
CMV promoter CMV_8F_10F aggaagagagTGATTTTATGGGATTTTTTTATTTGG 284
CMV_8F_T7R cagtaatacgactcactatagggagaaggctTTCTCTAATTAACCAAAAAACTCTACTT
EF‐1α promoter EF‐1α_2F_10F aggaagagagTTATTATTGAGGTGGAGAAGAGTATG 459
EF‐1α_2F_T7R cagtaatacgactcactatagggagaaggctCAAACCAAACCTCAACTCAAACA
Dnmt3a for qPCR F CGATGAACCGGAGTACGAGG 179
R CCACTGAGAACTTGCCGTCT
GAPDH for qPCR F CCGCATCCCTGAGACAAGAT 175
R TGCCGTGGGTGGAATCATAC