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. 2003 Jan;185(2):444–452. doi: 10.1128/JB.185.2.444-452.2003

TABLE 1.

Primers used in this study

Primer Primer sequence (5′ → 3′)a Coordinates
SpoT F1 TTT TTG TCG ACG AGC TC∗C GGT AGT GGA TGA GC 195219-195233b
SpoT F2 TT GCA CAT TTA ATC AAG ATA AAT G 195713-195736b
SpoT R1 CGG ATT AGC TGG CAC AT 196044-196028b
SpoT R2 TTT TTC TGC AG∗G GTT TTG TTC TAA AGA ATC ATC C 198165-198142b
RT F −25 GAA AAG AGA GCA AGG GCG CTG ATA 195657-195680b
RT F −50 ACA TTT AAA AAC AAT TTA CGA TCT T 195632-195656b
RT R +800 TAA GTT TGT TTG TTC TTG TTT GCA T 196507-196483b
RT R +850 TTT TGT TTT TTG CAA ATT ATT CTT A 196556-196532b
RT R +950 TTG ATA TTT ATT TTC TTT TGG GCT T 196656-196632b
OspA F1 GGG AAT AGG TCT AAT ATT AGC CTT 9411-9434c
OspA R1 CTG CTG ACC CCT CTA ATT TGG TGC C 10171-10147c
a

Bold letters indicate recognition sites for the restriction endonucleases used. SpoT F1 includes SacI and SalI sites. SpoT R2 contains a PstI site. ∗ indicates the start of the B. burgdorferi-specific sequence.

b

Coordinates from B. burgdorferi main chromosome.

c

Coordinates from B. burgdorferi linear plasmid 54 (lp54).