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Table 3 Primers used in this study

From: Recovery of recombinant Mycobacterium tuberculosis antigens fused with cell wall-anchoring motif (LysM) from inclusion bodies using non-denaturing reagent (N-laurylsarcosine)

Fragment

Primer sequence (5′ to 3′)a

Expected product size (base pair)

ARL

Forward GGATCCGAATTCGCTGACCAGCGAGCTGCCGC

1244

Reverse GCGGCCGCTTATTTTATTCGTAGATACTGAC

 

lysM

Forward CTGCAGCCATGGCGGCTGGAAGACGAGATGAAA

608

Reverse GCGGCCGCTTATTTTATTCGTAGATACTGAC

 

AR

Forward GGATCCGAATTCGCTGACCAGCGAGCTGCCGC

613

Reverse GCGGCCGCTGGCTTCCCTTCCGAAACCGC

 

Reverse CTGCAGGCTGGCTTCCCTTCCGAAACCGC

 

pRSF:Duet-1

Forward GGATCTCGACGCTCTCCCT

200

Reverse TTGTACACGGCCGCATAATC

 
  1. aRestriction enzyme (RE) sites are shown as bold and underlined is either BamHI (GGATCC), PstI (CTGCAG) or NotI (GCGGCCGC)