Detection and quantitation of unlabeled nucleic acids in polyacrylamide gels.
نویسندگان
چکیده
A method for the detection and quantitation of unlabeled nucleic acids in polyacrylamide gels is presented. The technique is a variation on UV shadowing. The technique is based on the observation that some storage phosphor screens (Kodak in this case) are sensitive to UV light in the range where nucleic acids absorb most strongly. Nucleic acid present in a gel resting on the screen absorbs the UV light and casts an ultraviolet shadow on the storage phosphor screen. The amount of nucleic acid in a particular area of the polyacrylamide gel is inversely proportional to the average pixel intensity in the corresponding area of the image. The technique therefore provides an electronic record of the gel in addition to the ability to quantitate the amount of nucleic acid present in any particular band. The storage phosphor screen images are erased by visible light. If the passage of that light to the screen is blocked by the presence of solid objects or images, the reverse process can be achieved, i.e., the recording of positive images by visible light etching of a uniformly charged background. By this method, we are able to transform old autoradiographic data into digital form for easy storage, computerized manipulation and distribution.
منابع مشابه
Oligonucleotide microchips as genosensors for determinative and environmental studies in microbiology.
The utility of parallel hybridization of environmental nucleic acids to many oligonucleotides immobilized in a matrix of polyacrylamide gel pads on a glass slide (oligonucleotide microchip) was evaluated. Oligonucleotides complementary to small-subunit rRNA sequences of selected microbial groups, encompassing key genera of nitrifying bacteria, were shown to selectively retain labeled target nuc...
متن کاملDetection of labelled RNA species by contact hybridization.
An improved contact hybridization technique for the analysis of labelled RNA species is presented. The method combines high sensitivity of detection with the high resolution of polyacrylamide gel electrophoresis and should be especially useful for the characterization of transient RNA precursor molecules. Its application to gene mapping is illustrated.
متن کاملTransfer of small plasmid DNA fragments from polyacrylamide gels onto nitrocellulose paper.
The incorporation into a 7% polyacrylamide gel of a nucleic acid-specific photochemical reagent 4,5',8-trimethylpsoralen at a concentration of 1 mg/dl of acrylamide solution improves both the sensitivity and the efficiency of the transfer of plasmid DNA fragments from the gel onto nitrocellulose filters. This improvement allows detection by blot hybridization of DNA fragments as small as 57 bp ...
متن کاملA simple system for staining protein and nucleic acid electrophoresis gels.
Researchers in molecular biology spend a significant amount of time tending to the staining and destaining of electrophoresis gels. Here we describe a simple system, costing approximately $100 and taking approximately 1 h to assemble, that automates standard nucleic acid and protein gel staining protocols. Staining is done in a tray or, with DNA gels, in the electrophoresis chamber itself follo...
متن کاملMutation typing using electrophoresis and gel-immobilized Acrydite probes.
A new electrophoresis technology for hybridization-based sequence detection and mutation typing is described. Intrinsic to this approach is copolymerization of specially modified oligonucleotide probes directly into polyacrylamide gels. Electrophoresis of single-stranded samples through gels containing specific immobilized probes results in hybridization-mediated capture of complementary target...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- BioTechniques
دوره 20 2 شماره
صفحات -
تاریخ انتشار 1996