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. 2000 Jan;38(1):345–350. doi: 10.1128/jcm.38.1.345-350.2000

TABLE 5.

AmpliTaq Gold and rTth DNA polymerase detection sensitivity in water and in the presence of PIgG and effects of heating of PIgG and L. monocytogenes DNA together and adding bacteriophage λ DNAa

Amt of L. monocytogenes DNA (g)/reaction tube PCR resultb
Water
IgGc
Heated IgG, AmpliTaqd Heated IgG and DNAe
IgG and λ DNA,f AmpliTaq
AmpliTaq rTth AmpliTaq rTth AmpliTaq rTth
10−6 + + + + + + + +
10−7 + + + + + + +
10−8 + + + + +
10−9 + + ± ± +
10−10 + + +
10−11 + + +
10−12
a

Ability of AmpliTaq Gold and rTth DNA polymerases to amplify different concentrations of L. monocytogenes DNA in water and in the presence of 0.41 μg PIgG and the effects of heating PIgG together with different concentrations of L. monocytogenes DNA and the addition of 1.25 ng of bacteriophage λ DNA on the detection level. 

b

PCR results: +, band of high intensity; ±, band of low intensity; −, no band. 

c

PCR detection in the presence of 0.41 μg of PIgG. 

d

PCR detection in the presence of 0.41 μg of PIgG heated at 95°C for 10 min. 

e

PCR detection in the presence of 0.41 μg of PIgG heated together with L. monocytogenes DNA at 95°C for 10 min. 

f

PCR detection in the presence of 0.41 μg of PIgG and 1.25 ng of bacteriophage λ DNA.