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. 2022 Oct 3;323(6):C1720–C1727. doi: 10.1152/ajpcell.00294.2022

Table 1.

Primers used in the study

Primers used for cloning 3´UTR-NHE-3 in pmirGLO vector:
 Forward: 5′-ACTGCTAGCCACCGGCTCCGACACGCCGCTAAC-3′
 Reverse: 5′-ACTCTCGAGGGAGTTCTGCGCAGGCGCTGGCGT-3′
Real time PCR primers:
 NHE-3:
  Forward: 5′-ACCTGTTCGTCAGCACCAC-3′.
  Reverse: 5′-GCTCGCTCCTCTTCACCTT-3′
 GAPDH:
  Forward: 5′-GAAATCCCATCACCATCTTCC-3′.
  Reverse: 5′-AAATGAGCCCCAGCCTTCT-3′
Forward primers used for quantifying microRNA expression:
 hsa-miR-204: 5′-TTCCCTTTGTCATCCTATGCCT-3′
 hsa-miR-326: 5′-CCTCTGGGCCCTTCCTCCAG-3′
 hsa-miR-330-5P: 5′-TCTCTGGGCCTGTGTCTTAGGC-3′
 hsa-miR-744-5p: 5′-TGCGGGGCTAGGGCTAACAGCA-3′
 U6B: 5′-CGCAAGGATGACACGCAAATTCG-3′
A common universal reverse primer provided in the kit was used

NHE-3, sodium hydrogen exchanger-3; 3′UTR, 3′ untranslated region.