Skip to main content
. 2015 Sep 30;35(21):3701–3713. doi: 10.1128/MCB.00219-15

TABLE 2.

Oligonucleotide primers and probes used for detection of the RAG binding sequencea

Region Sequence
Forward primer Hydrolysis probe Reverse primer
Jκ1 5′-TTGTACAGCCAGACAGTGGAG-3′ 5′-TGGTGCCTCCACCGAACGTC-3′ 5′-GCCACAGACATAGACAACGG-3′
Jκ2 5′-CAGATTCTGGCACTCTCCAA-3′ 5′-CAAAGAAGCAGGGTAGCCTGCCC-3′ 5′-ACTGAGCATGGTCTGAGCAC-3′
Jκ5 5′-CATAGTCCTCACTGTGGCTCA-3′ 5′-CTTGGTCCCAGCACCGAACG-3′ 5′-AGTGTACTTACGTTTCAGCTCCA-3′
Pou2af1 5′-ATCTCCGATTCTGTGCATGA-3′ 5′-AATCTGCCCTTCTGTCACCTCAGTGA-3′ 5′-GTGAAGAACGGCTCCTAACC-3′
γ-Actin 5′-CCTCCTCCAATAAAGGGACA-3′ 5′-AGAACTGGTGACCCTCTCCCACG-3′ 5′-GCCATCACATCCCAGTCA-3′
α-Actin 5′-GGCACGTGACACTCTTGTCT-3′ 5′-ATCGGTGGCTCCATCCTGGC-3′ 5′-GTCGTACTCCTGCTTGGTGA-3′
12a 5′-CCTCTAGACTGCCGGATCTC-3′ 5′-TCCCTCCTCCAAGCCCTGGA-3′ 5′-CATAAGCCTGCTGGTTCAGA-3′
23d 5′-GCAAGACTGAGAGCAGGAGA-3′ 5′-CCGTCCTCGAGGCACCATGA-3′ 5′-ACACCGGCCTTATTCCAA-3′
a

Hydrolysis probes were labeled at the 5′ end with the reporter dye 6-carboxyfluorescein (FAM) and at the 3′ end with black hole quencher (BHQ) dye (Biosearch Technologies).