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. 2012 Apr 9;7(4):e35243. doi: 10.1371/journal.pone.0035243

Table 1. Primer sequences for generation and characterization of TgUICBAC mice.

Primers (5′→3′) and Applications
ATTGGCCCCAGGAAACCCCAGCCTGTCAGCACCTGTTCCAGGATCCAGTTCCCAGCGCAGTATGgatatctccaacctgctg (forward)GAGCCAGGACAGCCAGCAGAATCAGGATCAGGGGCAAGGTCTGGACAGGCAGTGTGGATGCgctagccgttaattaagaag (reverse)Using pIndu-perfect as a template to get a 3498 bp iCreERT2 Cassette. Capital letters are from Upk2 sequence, lower-case letters are from iCreERT2 sequence.
CTGAGGCTACAGTGCCCAAG (forward)GTCTAGCGCTCTGAAACCCTC (reverse)Using modified BAC DNA as a template to get a 3772 bp (or 274 bp for unmodified BAC) product.
cttatcgatgataagctgtcaaacatgagaattgatccggaacccttaatTCTTAGACGTCAGGTGGCAC (forward)ccgatgcaagtgtgtcgctgtcgacggtgaccctatagtcgagggacctaTCACGTTAAGGGATTTTGGT (reverse)Using pTAMP as a template to get a 860 bp Amp cassette to delete the loxp site in BACe3.6. Lower-case letters are from BAC3.6 sequence, capital letters are from Amp sequence.
ATGGATATCTCCAACCTGCTG (forward)AGATCTCCTGTGCAGCATG (reverse)Using tail genomic DNA to get a 312 bp product for TgUICBAC transgenic mice PCR genotyping.
TGCTCCCAGGTGGTGGATCTC (forward)CTCAAAGCGGACCTCCTGTTC (reverse)Using BAC DNA as a template to get a 389 bp probe for Southern blot genotyping. Using the probe and ScaI digestion to get 8869 bp and 11196 bp for transgenic and Wt allele on Sothern blot, respectively.
CGCGAGAGGAGTGTGTCTG (forward)CTCTGAATCGAGGGATGGAGT (reverse)qRT-PCR for Bcl9l
AGGCCGAGCAGAAACTTGC (forward)GGCTTAATGTCTGGACCATCTTT (reverse)qRT-PCR for Foxr1
TGGCCTTCTACAGTAACAGCA (forward)GCATGAATACCGCCTTAAAGGAC (reverse)qRT-PCR for Cxcr5
AGGTCGGTGTGAACGGATTTG (forward)GGGGTCGTTGATGGCAACA (reverse)qRT-PCR for Gapdh