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WFRF:(Quackenbush J.)
 

Sökning: WFRF:(Quackenbush J.) > Monitoring of repre...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003207naa a2200457 4500
001oai:DiVA.org:kth-21614
003SwePub
008100810s2002 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-216142 URI
024a https://doi.org/10.2144/02326mt062 DOI
040 a (SwePub)kth
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Andersson, T.4 aut
2451 0a Monitoring of representational difference analysis subtraction procedures by global microarrays
264 1b Future Science Ltd,c 2002
338 a print2 rdacarrier
500 a QC 20100525
520 a Various approaches to the study of differential gene expression are applied to compare cell lines and tissue samples in a wide range of biological contexts. The compromise between focusing on only the important genes in certain cellular processes and achieving a complete picture is critical for the selection of strategy. We demonstrate how global microarray technology can be used for the exploration of the differentially expressed genes extracted through representational difference analysis (RDA). The subtraction of ubiquitous gene fragments from the two samples was demonstrated using cDNA microarrays including more than 32 000 spotted, PCR-amplified human clones. Hybridizations indicated the expression of 9100 of the microarray elements in a macrophage/foam cell atherosclerosis model system, of which many were removed during the RDA process. The stepwise subtraction procedure was demonstrated to yield an efficient enrichment of gene fragments overrepresented in either sample (18% in the representations, 86% after the first subtraction, and 88% after the second subtraction), many of which were impossible to detect in the starting material. Interestingly, the method allowed for the observation of the differential expression of several members of the low-abundant nuclear receptor gene family. We also observed a certain background level in the difference products of nondifferentially expressed gene fragments, warranting a verification strategy for selected candidate genes. The differential expression of several genes was verified by real-time PCR.
653 a polymerase chain-reaction
653 a gene-expression
653 a tangier-disease
653 a messenger-rna
653 a oxidized ldl
653 a ppar-gamma
653 a cdna
653 a hybridization
653 a differentiation
653 a cholesterol
700a Unneberg, P.4 aut
700a Nilsson, Peteru KTH,Bioteknologi4 aut0 (Swepub:kth)u1ws88sk
700a Odeberg, Jacobu KTH,Bioteknologi4 aut0 (Swepub:kth)u1e4yljo
700a Quackenbush, J.4 aut
700a Lundeberg, Joakimu KTH,Bioteknologi4 aut0 (Swepub:kth)u1qkn9kw
710a KTHb Bioteknologi4 org
773t BioTechniquesd : Future Science Ltdg 32:6, s. 1348-+q 32:6<1348-+x 0736-6205x 1940-9818
856u https://www.future-science.com/doi/pdf/10.2144/02326mt06
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-21614
8564 8u https://doi.org/10.2144/02326mt06

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