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Table 2 List of the primers used for cloning and gene expression in this study

From: The immune-adjunctive potential of recombinant LAB vector expressing murine IFNλ3 (MuIFNλ3) against Type A Influenza Virus (IAV) infection

Target gene

Purpose

Primer sequence

Amplicon size (bp)

Annealing temperature (°C)

Source

MuIFNλ3

Cloning into pHis-TEV Plasmid

F-5′ATAGGATCCATGCTCCTCCTGCTG 3′

R-5′ATAAAGCTTTTATCAGACACACTGGTCTC 3′

582

60

This study

MuIFNλ3

Cloning into pSec Plasmid

F-5′ ACTATGCATCAGAGATGCTCCTCCTGCTGTT 3′

R-5′GATGCTAGCTTATCAGACACACTGGTCTCC 3′

582

59

This study

MuGAPDH

Semi-quantitative PCR

F-5′CGTGCCGCTGGAGAAACC 3′

R-5′TGGAAGAGTGGGAGTTGCTGTTG 3′

150

60

This study

MuMX-1

Semi-quantitative PCR

F-5′GAAGGCAAGGTCTTGGATG 3′

R-5′GCTGACCTCTGCACTTGACT 3′

82

60

This study

MuISG-15

Semi-quantitative PCR

F-5′AGCAATGGCCTGGGACCTAAA3′

R-5′AGCCGGCACACCAATCTT 3′

124

55

This study

MuIRF-7

Semi-quantitative PCR

F-5′CCCAGACTGCCTGTGTAGACG 3′

R-5′CCAGTCTCCAAACAGCACTCG 3′

71

55

This study

MuIL-4

Semi-quantitative PCR

F-5′GGTCTCAACCCCCAGCTAGT3′

R-5′GCCGATGATCTCTCTCAAGTGAT3′

102

60

This study

MuIL-6

Semi-quantitative PCR

F-5′TAGTCCTTCCTACCCCAATTTCC3′

R-5′TTGGTCCTTAGCCACTCCTTC3′

76

60

This study

MuIL-10

Semi-quantitative PCR

F-5′GCTCTTACTGACTGGCATGAG 3′

R-5′CGCAGCTCTAGGAGCATGTG 3′

105

53

This study

Influenza M-gene universal primer

Real Time quantitative PCR

F-5′ATGAGTCTTCTAACCGAGGTCGAAACG 3′

R-5′TGGACAAAGCGTCTACGCTG 3′

242

60

(Kuchipudi et al., 2012)