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Table 1 Primers and templates used in generation of deletion and truncated mutants for luciferase activity test

From: Molecular cloning, polymorphism, and functional activity of the bovine and water buffalo Mx2 gene promoter region

Construct

Primer name

Primer type

Template

pGL3-(−422)

bMx2 p 422 + KpnI

5′-AGAGGTACCCCGTGGAGGAGCTGTGGATGTC

Forward

Genomic DNA

 

bMx2 p 20 + XhoI

5′-AGACTCGAGCCTGTGCACTTGTAGGAGGG

Reverse

 

pGL-(−154)

bMx2 p154 + KpnI

5′-AGAGGTACCCGCTTCAGGTTTCATTTCTG

Forward

Genomic DNA

 

bMx2 p 20 + XhoI

5′-AGACTCGAGCCTGTGCACTTGTAGGAGGG

Reverse

 

pGL-(−132)

bMx2 p132 KpnI

5′-AGAGGTACCGCAGGCTAATGGTTTCGTTT

Forward

Genomic DNA

 

bMx2 p 20 + XhoI

5′-AGACTCGAGCCTGTGCACTTGTAGGAGGG

Reverse

 

pGL-(−109)

bMx2 p109 + KpnI

5′-AGAGGTACCGGGCAAGCCATTAGTTTCAT

Forward

Genomic DNA

 

bMx2 p 20 + XhoI

5′-AGACTCGAGCCTGTGCACTTGTAGGAGGG

Reverse

 

pGL-(−76)

bMx2 p76 + KpnI

5′-AGAGGTACCGGGAAAGCAAGCCACGAG

Forward

Genomic DNA

 

bMx2 p 20 + XhoI

5′-AGACTCGAGCCTGTGCACTTGTAGGAGGG

Reverse

 

pGL-ΔISRE1 + 2

bMx2 p84F

5′-TTACTTCTGGGAAAGCAAGC

Forward

pGL-(−154)

 

bMx2 p127

5′-GCCTGCCACAGAAATGAAAC

Reverse

 

pGL-ΔISRE1

bMx2 p84F

5′-TTACTTCTGGGAAAGCAAGC

Forward

pGL-(−154)

 

bMx2 p99

5′-ATGGCTTGCCCTAGAAACG

Reverse

 

pGL-ΔISRE2

bMx2 p109

5′-GGGCAAGCCATTAGTTTCAT

Forward

pGL-(−154)

 

bMx2 p127

5′-GCCTGCCACAGAAATGAAAC

Reverse