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. Author manuscript; available in PMC: 2019 Nov 1.
Published in final edited form as: J Cell Biochem. 2018 Jul 16;119(11):9334–9345. doi: 10.1002/jcb.27212

Table 1.

Primers used for genotyping by PCR.

Allele Strand Sequence Amplicon Size (bp)
Lyz2Cre Forward1
Forward2
Reverse
5′-TTACAGTCGGCCAGGCTGAC-3′ Lyz2WT = 350
Lyz2Cre = 700
5′-CCCAGAAATGCCAGATTACG-3′
5′-CTTGGGCTGCCAGAATTTCTC-3′
Nfatc2loxP Forward
Reverse
5′-GGTGTCTCCCTCAAATGTTCA-3′
5′-GCGAATATGAGGACCCAAGT-3′
WT = 160
Nfatc2loxP= 250
Frt and LoxP recombination Strand Sequence Amplicon Size (bp)
Frt recombination of Nfatc2 targeted allele Forward
Reverse
5′-AGTATGTAACCTCTGCTTCC-3′
5′-AGCACAATGCCCATGTTCAC-3′
WT = 250
Not recombined = no band
Recombined = 351 (Nfatc2loxP)
LoxP recombination of Nfatc2loxP Reverse
Forward
5′-GGTGTCTCCCTCAAATGTTCA-3′
5′-AGCACAATGCCCATGTTCAC-3′
Not recombined = 2342 (Nfatc2loxP)
Recombined = 358 (Nfatc2Δ)