RNA preparation and characterization for gene expression studies

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Standard

RNA preparation and characterization for gene expression studies. / Stangegaard, Michael.

Methods in Molecular Biology: DNA Microarrays for Biomedical Research. red. / Hans Martin Dufva. Bind 529 1. udg. New York, NY : Springer Science+Business Media, 2009. s. 115-132.

Publikation: Bidrag til bog/antologi/rapport › Bidrag til bog/antologi › Undervisning

Harvard

Stangegaard, M 2009, RNA preparation and characterization for gene expression studies. i HM Dufva (red.), Methods in Molecular Biology: DNA Microarrays for Biomedical Research. 1 udg, bind 529, Springer Science+Business Media, New York, NY, s. 115-132. https://doi.org/10.1007/978-1-59745-538-1_8

APA

Stangegaard, M. (2009). RNA preparation and characterization for gene expression studies. I H. M. Dufva (red.), Methods in Molecular Biology: DNA Microarrays for Biomedical Research (1 udg., Bind 529, s. 115-132). Springer Science+Business Media. https://doi.org/10.1007/978-1-59745-538-1_8

Vancouver

Stangegaard M. RNA preparation and characterization for gene expression studies. I Dufva HM, red., Methods in Molecular Biology: DNA Microarrays for Biomedical Research. 1 udg. Bind 529. New York, NY: Springer Science+Business Media. 2009. s. 115-132 https://doi.org/10.1007/978-1-59745-538-1_8

Author

Stangegaard, Michael. / RNA preparation and characterization for gene expression studies. Methods in Molecular Biology: DNA Microarrays for Biomedical Research. red. / Hans Martin Dufva. Bind 529 1. udg. New York, NY : Springer Science+Business Media, 2009. s. 115-132

Bibtex

@inbook{f77fe360923111de8bc9000ea68e967b,
title = "RNA preparation and characterization for gene expression studies",
abstract = "Much information can be obtained from knowledge of the relative expression level of each gene in the transcriptome. With the current advances in technology as little as a single cell is required as starting material for gene expression experiments. The mRNA from a single cell may be linearly amplified to an excess of 10(6)-fold. Reverse transcription and fluorescent labeling of the amplified RNA yields a stable target for subsequent hybridization to DNA microarrays.",
keywords = "Faculty of Social Sciences",
author = "Michael Stangegaard",
note = "ikke relevant",
year = "2009",
doi = "10.1007/978-1-59745-538-1_8",
language = "English",
isbn = "1064-3745",
volume = "529",
pages = "115--132",
editor = "Dufva, {Hans Martin}",
booktitle = "Methods in Molecular Biology",
publisher = "Springer Science+Business Media",
address = "Singapore",
edition = "1",

}

RIS

TY - CHAP

T1 - RNA preparation and characterization for gene expression studies

AU - Stangegaard, Michael

N1 - ikke relevant

PY - 2009

Y1 - 2009

N2 - Much information can be obtained from knowledge of the relative expression level of each gene in the transcriptome. With the current advances in technology as little as a single cell is required as starting material for gene expression experiments. The mRNA from a single cell may be linearly amplified to an excess of 10(6)-fold. Reverse transcription and fluorescent labeling of the amplified RNA yields a stable target for subsequent hybridization to DNA microarrays.

AB - Much information can be obtained from knowledge of the relative expression level of each gene in the transcriptome. With the current advances in technology as little as a single cell is required as starting material for gene expression experiments. The mRNA from a single cell may be linearly amplified to an excess of 10(6)-fold. Reverse transcription and fluorescent labeling of the amplified RNA yields a stable target for subsequent hybridization to DNA microarrays.

KW - Faculty of Social Sciences

U2 - 10.1007/978-1-59745-538-1_8

DO - 10.1007/978-1-59745-538-1_8

M3 - Book chapter

C2 - 19381966

SN - 1064-3745

SN - 978-1-934115-69-5

VL - 529

SP - 115

EP - 132

BT - Methods in Molecular Biology

A2 - Dufva, Hans Martin

PB - Springer Science+Business Media

CY - New York, NY

ER -

ID: 13973983