- Double stranded DNA quantiﬁcation performed in down to 2 µl using the LVis Plate
- High linearity and sensitivity over a broad DNA range
- Easy to use UV absorbance alternative assay that can be miniaturized and adapted to high-throughput systems
Table of contents
The quantiﬁcation of nucleic acids samples is a major need in any genetic and molecular biology laboratory. Next to well-known UV absorbance assays (e.g. 260/280 nm), a lot of different ﬂuorescence intensity based DNA quantiﬁcation assays are offered. These assays are not only more sensitive than absorbance assays, they are also able to differentiate between double-stranded and single-stranded DNA, as well as RNA.
Aside from sensitivity and speciﬁcity, the demand for very low volume measurements is emerging. This is challenging for assays as well as for the detection instrumentation. In this application note we present DNA quantiﬁcation data obtained on the low volume LVis Plate, as well as 96- and 384-well microplates.
Materials & Methods
- Quant-iT™ PicoGreen® dsDNA assay, LifeTechnologies
- Low volume LVis Plate, BMG LABTECH
- Black 96-well and 384-well microplates, Greiner
All necessary reagents such as detection reagent, TE buffer, DNA standard (Lambda DNA standard) are provided with the kit. From a 20x TE buffer stock solution a 1x TE buffer was prepared using HPLC grade water. The PicoGreen® reagent was diluted 1:200 by using 1x TE buffer. dsDNA standards were diluted with 1x TE buffer to obtain a concentration range of 2 to 1000 ng/ml. DNA standards were pipetted in 6 replicates, adding the same amount of PicoGreen® reagent into each well leading to the ﬁnal volumes: 200 µl in 96-well plates, 20 µl in 384-well plates and 2 µl in the LVis Plate. The blank consisted of TE buffer.
|FLUOstar/ POLARstar Omega||CLARIOstar||PHERAstar FS|
|Filter settings||Ex485 |
|Optic Module: |
FI 485 520
|Monochromator settings||Ex: 483-14 |
All other settings are default settings for a ﬂuorescence endpoint test protocol.
Results & Discussion
Fluorescence scan of PicoGreen® reagent bound to DNA
In order to determine useful monochromator settings for the CLARIOstar, an excitation and emission scan was done for the DNA bound PicoGreen® reagent. The spectra scan result is shown in Fig. 1.
The scan showed an excitation maximum at 502 nm and an emission maximum at 524 nm. For further measurements, the highest signal/blank ratio was determined by varying the band widths for excitation and emission.
In 96-well plates the standard curves obtained using either ﬁlters or the monochromator are very similar (Fig. 2). With ﬁlters the slope of the standard curve is slightly higher.
To miniaturize the assay, the well volume was decreased to 20 µl. The resulting standard curve in 384-well small volume plate (Fig. 3) was comparable to the data obtained for 96-well plates.
Very good linearity was achieved for the CLARIOstar using either ﬁlters (R2 = 0.9999) or LVF Mono-chromators™ (R2 = 0.9998).
LVis Plate results
With the LVis Plate it is possible to miniaturize the assay further. This special plate was developed to use a volume of as little as 2 µl.
Originally developed to do DNA and protein UV absorbance quantiﬁcation the LVis Plate, used in the CLARIOstar or PHERAstar FS, is an excellent tool to determine the DNA content of samples in ﬂuorescence intensity mode. Results for the PicoGreen® assay in the LVis Plate are shown in Fig. 4.
The standard curve data show that the PicoGreen® assay can be measured with high linearity and sensitivity over a broad DNA concentration range. For the CLARIOstar, the LVF Monochromator™ shows ﬁlter-like performance. For example, the sensitivity in 384-well plates was calculated to be about 3 pg/well for both ﬁlters and LVF Monochromators™.
With the help of the PicoGreen® assay, any preferred volume, between 2 µl in the LVis Plate or standard volumes in 96- and 384-well plates, can be used to determine the DNA concentration of samples.
PicoGreen is a registered trademark of Invitrogen.