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Table 1 PCR primers for amplification of chIFN-α, chIL-18, AIH9, IFN-γ, IL-4, and GAPDH

From: Enhancement of Th1-biased protective immunity against avian influenza H9N2 virus via oral co-administration of attenuated Salmonella enterica serovar Typhimurium expressing chicken interferon-α and interleukin-18 along with an inactivated vaccine

Target gene

 

Primer sequence (5′-3′)

Accession no.

Reference

chIFN-α a

F

ATGGCTGTGCCTGCAAGCCCA

DQ026259.1

-

 

R

CTAAGTGCGCGTGTTGCCTGT

  

chIL-18 b

Fc

GAATTCGCCTTTTGTAAGGATAAAACT

HM854281.1

-

 

Rc

AAGCTTTCAGTGATGGTGATGGTGATG TAGGTTGTGCCTTTC

  

AIH9

F

CTACTGTTGGGAGGAAGAGAATGGT

AF461510.1

[29]

 

R

TGGGCGTCTTGAATAGGGTAA

  

IFN-γ

F

CAAAGCCGCACATCAAACA

X99774

[30]

 

R

TTTCACCTTCTTCACGCCATC

  

IL-4

F

GAGAGGTTTCCTGCGTCAAG

FJ907790.1

[31]

 

R

TGGTGGAAGAAGGTACGTAGG

  

GAPDH

F

AGAACATCATCCCAGCGTCC

X01578

[30]

 

R

CGGCAGGTCAGGTCAACA

  
  1. aThe primer pair specific for chIFN-α gene was designed using chIFN-α6 nucleotide sequences (Genbank accession number DQ026259.1), and the sequences of the two primers were checked using NCBI Blast Software.
  2. bThe primer pair specific for chIL-18 gene was designed using chIL-18 nucleotide sequences (Genbank accession number HM854281.1), and the sequences of the two primers were checked using NCBI Blast Software.
  3. cThe forward and reverse primers specific for chIL-18 gene contain EcoRI and HindIII restriction sites as indicated by the underline. The reverse primer also contained 6×His-Tag sequences indicated in boldface.