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Table 1 Primers used in this experiment

From: Characterization of Norwalk virus GI specific monoclonal antibodies generated against Escherichia coli expressed capsid protein and the reactivity of two broadly reactive monoclonal antibodies generated against GII capsid towards GI recombinant fragments

LI:

TCC CCCGGG ATG ATG ATG GCG TCT AAG GAC

L2:

GC TCTAGA TTA TWW WCG GCG CAV WCC AAG CC

G1:

TCC CCCGGG CTT GCA ATG GAT CCT GTG GC

Ql:

GC TCTAGA ACT GCT GTT GAA GAA CCC GC

G2:

TCC CCCGGG CAA GGT GAA TTT ACT ATT TC

Q2:

GC TCTAGA AAT AGT AAA TTC ACC TTG GG

G3:

TCC CCCGGG CTT AAT CCC TTC TTG TTA C

Q3:

GC TCTAGA TGC CAA CCC AGC CAT TAT AC

G4:

TCC CCCGGG GGT AAA ATT ATA GTT TCT TGC

Q4:

GC TCTAGA AAT CAC ATG CGG GAA GAG AG

G5:

TCC CCCGGG GAT GTA AGG AAT GTT CTC TTT C

Q5:

GC TCTAGA CTT ACA TCT ACT AAG GGT AC

G6:

TCC CCCGGG CAA ACA ATG CGC CTT GTG TGC

Q6:

GC TCTAGA GGA GGG GGG TGT AAA GCA TG

G7:

TCC CCCGGG ACT TGT CCT AGC CCC GAT TTC

Q7:

GC TCTAGA GTT CCA CTG TGG GAG GAA CC

G8:

TCC CCCGGG TTG TCA AAT TCA CGT GCC CC

Q8:

GC TCTAGA AAT TGG AAG AGG GGC ACG TG

G9:

TCC CCCGGG TGT ACC TTA GAT GGA CGA C

Q9:

GC TCTAGA GGT GGT ACC AAC AAG TCG TC

G10:

TCC CCCGGG GGT ACT TCT AAT GGT ACT GTG

Q10:

GC TCTAGA GGG GCA GGG CCT TCA AAA GG

G11:

TCC CCCGGG GAT TGG CAT ATT AAC ATG AC

Q11:

GC TCTAGA TGA GTC TGG CTA GAA TGT CC

G12:

TCC CCCGGG GGT TCA ATC CAG GCG AAT GG

Q12:

GC TCTAGA TAA GAA CAC CAA TGT AGT TG

G13:

TCC CCCGGG AAG ATC CCC AAC TAT GGG TC

Q13:

GC TCTAGA CTG TGA TGC TAG ACC CAT AG

G14:

TCC CCCGGG TTC ATG TCA AAG ATA CCA GG

Q14:

GC TCTAGA AAG CAC CAG GGC CTG GTA TC

G15:

TCC CCCGGG CCC ACT GTT GGT GAA GCC GC

Q15:

GC TCTAGA TAG TGG AGT AGG GCG GCT TC

G16:

TCC CCCGGG GAT GGT TTC CTA ACC TGT GTC

Q16:

GC TCTAGA GCT GGC CCC GTT AGG GAC AC

Trx-up: TTC CTC GAC GCT AAC CTG GC

Trx-DW: GTA AA CGA CGG CCA GTG CC

  1. G, L and Q primers were used for amplifying NV96-908 fragments, and Trx-up and Trx-dw primers for generating the insert and junction sequence of recombinant plasmids. These Trx primers have also been used for sequencing. Underlined sequences of G primers and LI primer shows the Sma I site, and that of bo th L2 primer and Q primers the Xba I site.