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tion statuses of the Oct3/4, Rex1 and NANOG promoter regions. In Takahashis 2006 iPS publication, it was discovered that these promotor regions were highly unmethylated. Instead of ordering individual oligos, these complete for 50 reactions for each gene. Each batch of primers is vigorously tested for oligo integrity.
Protocols
PCR protocol (using Allele-in-One Mix):
Volume 5 units 1l 1 l 1 l 5 l 1 l
Features
Pre-tested and complete set of PCR primers for: 3 promotor genes. All sequences are identical to those as published by Takahashi et al. in their 2006 publication in Cell that All oligos were produced in-house at Allele Biotech with quality control provided at uniform concentrations for easy reaction setup.
(20 M)
Nuclease-free water
of 50 l
References
1.
follows:
Primers Sequence GGT TTA AAA GGG TAA ATG TGA TTA TAT TTA CAA ACT ACA ACC ACC CAT CAA C GAG GTT GGA GTA GAA GGA TTG TTT TGG TTT CCC CCC TAA CCC ATC ACC TCC ACC ACC TAA TGG TTA GGT TGG TTT TAA ATT TTT G AAC CCA CCC TTA TAA ATT CTC AAT TA
Contents
3 pairs of PCR primers (50l of 20M oligo)