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Identification of Methylated Deoxyadenosines in Genomic DNA by dA6m DNA Immunoprecipitation

Authors: Magdalena J. Koziol
Magdalena J. KoziolAffiliation 1: Wellcome Trust Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, UK
Affiliation 2: Department of Zoology, University of Cambridge, Cambridge, UK
For correspondence: mjk39@cam.ac.uk
Bio-protocol author page: a3666
Charles R. Bradshaw
Charles R. BradshawAffiliation: Wellcome Trust Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, UK
Bio-protocol author page: a3667
George E. Allen
George E. AllenAffiliation: Wellcome Trust Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, UK
Bio-protocol author page: a3668
Ana S. H. Costa
Ana S. H. CostaAffiliation: Medical Research Council Cancer Unit, University of Cambridge, Hutchison/MRC Research Centre, Cambridge, UK
Bio-protocol author page: a3669
 and Christian Frezza
Christian FrezzaAffiliation: Medical Research Council Cancer Unit, University of Cambridge, Hutchison/MRC Research Centre, Cambridge, UK
Bio-protocol author page: a3670
date: 11/5/2016, 1143 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.1990.

[Abstract] dA6m DNA immunoprecipitation followed by deep sequencing (DIP-Seq) is a key tool in identifying and studying the genome-wide distribution of N6-methyldeoxyadenosine (dA6m). The precise function of this novel DNA modification remains to be fully elucidated, but it is known to be absent from transcriptional ...

Generation of Mitochondrial-nuclear eXchange Mice via Pronuclear Transfer

Authors: Robert A. Kesterson
Robert A. KestersonAffiliation: Department of Genetics, University of Alabama, Birmingham, USA
For correspondence: kesterso@uab.edu
Bio-protocol author page: a3629
Larry W. Johnson
Larry W. JohnsonAffiliation: Department of Genetics, University of Alabama, Birmingham, USA
Bio-protocol author page: a3630
Laura J. Lambert
Laura J. LambertAffiliation: Department of Genetics, University of Alabama, Birmingham, USA
Bio-protocol author page: a3631
Jay L. Vivian
Jay L. VivianAffiliation: Department of Pathology, University of Kansas Medical Center, Kansas City, USA
Bio-protocol author page: a3632
Danny R. Welch
Danny R. WelchAffiliation: Department of Cancer Biology, University of Kansas Cancer Center, Kansas City, USA
For correspondence: dwelch@kumc.edu
Bio-protocol author page: a3633
 and Scott W. Ballinger
Scott W. BallingerAffiliation: Division of Molecular and Cellular Pathology, University of Alabama, Birmingham, USA
For correspondence: sballing@uab.edu
Bio-protocol author page: a3634
date: 10/20/2016, 1460 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.1976.

[Abstract] The mitochondrial paradigm for common disease proposes that mitochondrial DNA (mtDNA) sequence variation can contribute to disease susceptibility and progression. To test this concept, we developed the Mitochondrial-nuclear eXchange (MNX) model, in which isolated embryonic pronuclei from one strain ...

A Quick, No Frills Approach to Mouse Genotyping

Author: Manuel E. Lopez
Manuel E. LopezAffiliation: Department of Developmental Biology, Stanford University, Stanford, USA
For correspondence: manduardo@gmail.com
Bio-protocol author page: a74
date: 8/5/2012, 12325 views, 1 Q&A
DOI: https://doi.org/10.21769/BioProtoc.244.

[Abstract] Mice are extremely powerful mammalian genetic model organisms for basic and medical research, but managing a colony of transgenic mice is time consuming and expensive, many times requiring the help of dedicated technicians. Slow and laborious genotyping procedures add to the hassle. Outsourcing is costly ...
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A Quick, No Frills Approach to Mouse Genotyping

Author: Manuel E. Lopez
Manuel E. LopezAffiliation: Department of Developmental Biology, Stanford University, Stanford, USA
For correspondence: manduardo@gmail.com
Bio-protocol author page: a74
date: 8/5/2012, 12325 views, 1 Q&A
DOI: https://doi.org/10.21769/BioProtoc.244.

[Abstract] Mice are extremely powerful mammalian genetic model organisms for basic and medical research, but managing a colony of transgenic mice is time consuming and expensive, many times requiring the help of dedicated technicians. Slow and laborious genotyping procedures add to the hassle. Outsourcing is costly ...

Generation of Mitochondrial-nuclear eXchange Mice via Pronuclear Transfer

Authors: Robert A. Kesterson
Robert A. KestersonAffiliation: Department of Genetics, University of Alabama, Birmingham, USA
For correspondence: kesterso@uab.edu
Bio-protocol author page: a3629
Larry W. Johnson
Larry W. JohnsonAffiliation: Department of Genetics, University of Alabama, Birmingham, USA
Bio-protocol author page: a3630
Laura J. Lambert
Laura J. LambertAffiliation: Department of Genetics, University of Alabama, Birmingham, USA
Bio-protocol author page: a3631
Jay L. Vivian
Jay L. VivianAffiliation: Department of Pathology, University of Kansas Medical Center, Kansas City, USA
Bio-protocol author page: a3632
Danny R. Welch
Danny R. WelchAffiliation: Department of Cancer Biology, University of Kansas Cancer Center, Kansas City, USA
For correspondence: dwelch@kumc.edu
Bio-protocol author page: a3633
 and Scott W. Ballinger
Scott W. BallingerAffiliation: Division of Molecular and Cellular Pathology, University of Alabama, Birmingham, USA
For correspondence: sballing@uab.edu
Bio-protocol author page: a3634
date: 10/20/2016, 1460 views, 0 Q&A
DOI: https://doi.org/10.21769/BioProtoc.1976.

[Abstract] The mitochondrial paradigm for common disease proposes that mitochondrial DNA (mtDNA) sequence variation can contribute to disease susceptibility and progression. To test this concept, we developed the Mitochondrial-nuclear eXchange (MNX) model, in which isolated embryonic pronuclei from one strain ...
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