POTĚŠILOVÁ, Michaela, Miroslav VAŘECHA, Lenka TESAŘOVÁ and Irena KRONTORÁD KOUTNÁ. Time lapse living cells microscopy for studying CML: Preparation of Abl1- and Bcr/Abl - fluorescent protein vectors using Gateway technology. In Advances in Molecular and Cancer Biology, 2010. Brno: muni PRESS, 2010, p. 31-35. ISBN 978-80-210-5312-0.
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Basic information
Original name Time lapse living cells microscopy for studying CML: Preparation of Abl1- and Bcr/Abl - fluorescent protein vectors using Gateway technology
Authors POTĚŠILOVÁ, Michaela (203 Czech Republic), Miroslav VAŘECHA (203 Czech Republic), Lenka TESAŘOVÁ (203 Czech Republic) and Irena KRONTORÁD KOUTNÁ (203 Czech Republic, guarantor).
Edition Brno, Advances in Molecular and Cancer Biology, 2010, p. 31-35, 5 pp. 2010.
Publisher muni PRESS
Other information
Original language English
Type of outcome Proceedings paper
Field of Study Genetics and molecular biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14330/10:00045378
Organization unit Faculty of Informatics
ISBN 978-80-210-5312-0
Keywords in English Gateway cloning ABL1 BCR/ABL expression vectors
Tags cbia-web
Tags Reviewed
Changed by Changed by: Mgr. Michaela Potěšilová, učo 106117. Changed: 16/11/2010 14:34.
Abstract
Using time-lapse microscopy, protein localization and dynamics can be studied directly in living cells. This may bring significant information necessary to complete understanding of protein function. Aberrant tyrosinkinase Bcr/Abl is the main cause of chronic myelogenous leukemia. Abl1 tyrosinkinase represents its native form. Among others these natural and aberrant kinase differ in cell localization, which will be the subject for subsequent examination in the K562 leukemic cell line or in CD34+ cells from bone marrow. We created a unique set of Bcr/Abl and Abl1 expression vectors tagged with EYFP or RFP sequences for examination of protein pools movements in the living cells. The Gateway cloning system was chosen for its flexibility and robustness. We applied two types of fluorescent protein to be able watch both forms of kinase simultaneously.
Links
MSM0021622430, plan (intention)Name: Funkční a molekulární charakteristiky nádorových a normálních kmenových buněk - identifikace cílů pro nová terapeutika a terapeutické strategie
Investor: Ministry of Education, Youth and Sports of the CR, Functional and molecular characteristics of cancer and normal stem cells - identification of targets for novel therapeutics and therapeutic strategies
2B06052, research and development projectName: Vytipování markerů, screening a časná diagnostika nádorových onemocnění pomocí vysoce automatizovaného zpracování multidimenzionálních biomedicínských obrazů (Acronym: Biomarker)
Investor: Ministry of Education, Youth and Sports of the CR, Determination of markers, screening and early diagnostics of cancer diseases using highly automated processing of multidimensional biomedical images
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