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. 2006 May 24;34(10):2864–2877. doi: 10.1093/nar/gkl382

Table 2.

Experimental conditions and results

Enzyme C U/ml DNA template Nsites NP N/NP × 100 <F> <L> LS LL ρS %
BpmI 20 ½-λ-L 17 136 2.3 (0.42) 29.6 (11.2) 777 (208) 60 3634 18 (12)
BsgI 30 ½-λ-L 31 465 1.7 (0.22) 26.9 (12.3) 645 (83) 45 3344 −3.2 (12)
BspMI 20 ½-λ-L 24 276 0.91 (0.14) 23.2 (10.3) 613 (124) 25 4494 −16 (9.0)
Cfr10I 100 ½-λ-L 56 1540 1.2 (0.052) 22.5 (12.4) 470 (89) 22 7444 −23 (5.9)
Eco57I 50 ½-λ-L 25 300 2.7 (0.19) 21.8 (11.2) 573 (103) 19 7512 −6.7 (11)
EcoRII 50 ½-λ-L 36 630 0.29 (0.026) 25.6 (12.2) 665 (176) 21 6940 −24 (10)
FokI 40 LBAC-B 26 325 0.79 (0.038) 14.8 (11.0) 301 (61) 18 4120 −22 (5.6)
HpaII 100 LBAC-B 49 1176 0.51 (0.041) 16.6 (9.92) 325 (65) 20 2500 −23 (6.9)
Sau3AI 40 LBAC-A 55 1485 0.66 (0.041) 25.0 (10.8) 423 (85) 7 2682 −11 (5.1)

Nsites is the number of recognition sites on the DNA template; C is the enzyme concentration in U/ml; NP is the number of pairs of sites that can form loops on the DNA template; N/NP is the number of observed loops per molecule normalized by NP (and standard error); <F> is the mean loop disruption force (and SD) in pN; <L> is the mean observed loop size in base pairs (and SD) for the normalized distributions (see text); LS is the shortest observed event size in the ensemble of data; LL is the longest observed event size; ρS is the correlation coefficient between disruption force and event size for events <150 bp (and the SD expected for uncorrelated data).