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. 2013 Mar 8;42(5):1551–1559. doi: 10.3892/ijo.2013.1854

Table II.

Used primers and hydrolysis probes in this study.

Sequence (5′→3′)
For PCR analysis
  ABCB6
    5′-primer GGACCAAGATGTGGAAAGGA
    3′-primer CCAAAATCTCGCCAGGTAGA
    Hydrolysis probe UPL probe no. 66a
  GAPDH
    5′-primer AGCCACATCGCTCAGACAC
    3′-primer GCCCAATACGACCAAATCC
    Hydrolysis probe UPL probe no. 60a
  ACTB
    5′-primer CCAACCGCGAGAAGATGA
    3′-primer CCAGAGGCGTACAGGGATAG
    Hydrolysis probe UPL probe no. 64a
For qMSP analysisb
  ABCB6-MSP1 (position: −327 to −207)
    5′-primer GGGGTTATAGTcgTGGAGc
    3′-primer AAAACAcgTAcgCcgTCT
    Hydrolysis probe FAM-GTGGGTTTGTAGTTGGTAGGAGGGTT-BHQ
  ABCB6-MSP2 (position: −710 to −607)
    5′-primer TAGATTTTTTGTTGTTTcgc
    3′-primer TCTAAAcgAcgACCTAAACA
    Hydrolysis probe FAM-AAGAGAAATGGGATGGGGATTTTG-BHQ
  RPPH1
    5′-primer AATGAGGTGTAGAAGGTTGATGGT
    3′-primer CATAATTAAATCACTTCCCACCAAA
    Hydrolysis probe UPL Probe no. 10a
a

Universal ProbeLibrary (Roche Applied Bioscience).

b

CpG sites are presented as lower case letters. Position was given relative to the first codon of ABCB6. Start site of the first exon of ABCB6 is positioned at −317.