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. 2019 Mar 27;10:569. doi: 10.3389/fimmu.2019.00569

Table 1.

PCR primers used in this study.

Gene name Primer Sequence
NKG2D RECEPTOR
FL_NKG2D Forward GCTGTATTCCTAAACTCATTATTCAACC
Reverse CTGCCAAGATCCATTTGTTG
Tr_NKG2D Forward TTCTGCTGCTTCATCGCTGT
Reverse TGGACTAATAGCAAAAATGTGACAA
Both_NKG2D Forward CCTCTCTGCGGTAGACGTG
Reverse GACATCTTTGCTTTTGCCATC
NKG2D LIGANDS
MICA Forward AGGGTCTGTGAGATCCATGAAGAC
Reverse CCTGACGTTCATGGCCAAGG
MICB Forward ACCTTGGCTATGAACGTCACA
Reverse CCCTCTGAGACCTCGC
ULBP-2 Forward GCAAGGATGTCTTGTGAGCA
Reverse GGCCACAACCTTGTCATTCT
HOUSEKEEPING GENES
β2-microglobulin Forward GGGTTTCATCCATCCATCCGACA
Reverse ACACGGCAGGCATACTCATC
β-actin Forward CTGAACCCCAAGGCCAAC
Reverse CAGAGGCGTACAGGGATAGC
18S RNA Forward GACTCAACACGGGAAACCTC
Reverse AGACAAATCGCTCCACCAAC

To analyze the mRNA expression of NKG2D receptor and ligand following PCR primers were used. Housekeeping genes were used as internal control. PCR primers were designed using the Web-based primer3 software (http://primer3.wi.mit.edu/) and purchased from TIB MOLBIOL.