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1.
Electrophoresis ; 21(1): 135-49, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10634480

RESUMO

In this paper we present the development of a DNA analysis system using a microfabricated channel device and a novel transmission imaging spectrograph which can be efficiently incorporated into a high throughput genomics facility for both sizing and sequencing of DNA fragments. The device contains 48 channels etched on a glass substrate. The channels are sealed with a flat glass plate which also provides a series of apertures for sample loading and contact with buffer reservoirs. Samples can be easily loaded in volumes up to 640 nL without band broadening because of an efficient electrokinetic stacking at the electrophoresis channel entrance. The system uses a dual laser excitation source and a highly sensitive charge-coupled device (CCD) detector allowing for simultaneous detection of many fluorescent dyes. The sieving matrices for the separation of single-stranded DNA fragments are polymerized in situ in denaturing buffer systems. Examples of separation of single-stranded DNA fragments up to 500 bases in length are shown, including accurate sizing of GeneCalling fragments, and sequencing samples prepared with a reduced amount of dye terminators. An increase in sample throughput has been achieved by color multiplexing.


Assuntos
DNA/análise , DNA/genética , Eletroforese/métodos , Análise de Sequência de DNA/métodos , Animais , Sequência de Bases , Humanos , Processamento de Imagem Assistida por Computador , Dados de Sequência Molecular
2.
Nat Biotechnol ; 17(8): 798-803, 1999 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10429247

RESUMO

We describe an mRNA profiling technique for determining differential gene expression that utilizes, but does not require, prior knowledge of gene sequences. This method permits high-throughput reproducible detection of most expressed sequences with a sensitivity of greater than 1 part in 100,000. Gene identification by database query of a restriction endonuclease fingerprint, confirmed by competitive PCR using gene-specific oligonucleotides, facilitates gene discovery by minimizing isolation procedures. This process, called GeneCalling, was validated by analysis of the gene expression profiles of normal and hypertrophic rat hearts following in vivo pressure overload.


Assuntos
Bases de Dados Factuais , Expressão Gênica , RNA Mensageiro/genética , Animais , Cardiomegalia/genética , Cardiomegalia/patologia , Células HeLa , Humanos , Masculino , Ratos , Ratos Sprague-Dawley , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
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