Publication Date:
1995-10-20
Description:
A high-capacity system was developed to monitor the expression of many genes in parallel. Microarrays prepared by high-speed robotic printing of complementary DNAs on glass were used for quantitative expression measurements of the corresponding genes. Because of the small format and high density of the arrays, hybridization volumes of 2 microliters could be used that enabled detection of rare transcripts in probe mixtures derived from 2 micrograms of total cellular messenger RNA. Differential expression measurements of 45 Arabidopsis genes were made by means of simultaneous, two-color fluorescence hybridization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schena, M -- Shalon, D -- Davis, R W -- Brown, P O -- R21HG00450/HG/NHGRI NIH HHS/ -- R37AG00198/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 1995 Oct 20;270(5235):467-70.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Beckman Center, Stanford University Medical Center, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7569999" target="_blank"〉PubMed〈/a〉
Keywords:
Arabidopsis/*genetics
;
*Arabidopsis Proteins
;
DNA, Complementary/*genetics
;
DNA, Plant/genetics
;
DNA-Binding Proteins
;
*Gene Expression
;
*Genes, Plant
;
*Genetic Techniques
;
Genome, Human
;
Homeodomain Proteins
;
Humans
;
Molecular Sequence Data
;
Nucleic Acid Hybridization
;
Plant Leaves/genetics
;
Plant Roots/genetics
;
Plants, Genetically Modified
;
Polymerase Chain Reaction
;
RNA Probes
;
RNA, Messenger/genetics
;
RNA, Plant/genetics
;
Transcription Factors
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
Permalink