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A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression
by
Murach, Kevin A.
, Wen, Yuan
, Englund, Davis A.
, Mobley, Christopher B.
, Dungan, Cory M.
, McCarthy, John J.
, Vechetti, Ivan J.
, Iwata, Masahiro
, Peterson, Charlotte A.
in
Actin
/ Animals
/ Antibiotics
/ Biochemistry
/ Biomedical and Life Sciences
/ Biotechnology
/ Cell Biology
/ Cloning
/ Developmental Biology
/ Fluorescence
/ Gene expression
/ Gene Targeting - methods
/ Genes
/ Genetic engineering
/ Green fluorescent protein
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Histone H2B
/ Humans
/ Immunohistochemistry
/ Kinases
/ Life Sciences
/ Methodology
/ Mice
/ Mice, Inbred C57BL
/ Muscle proteins
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscles
/ Musculoskeletal system
/ PAX7 Transcription Factor - genetics
/ PAX7 Transcription Factor - metabolism
/ Reverse transcription
/ RNA
/ Rodents
/ Satellite cells
/ Skeletal muscle
/ Skeletal muscle-specific
/ Systems Biology
/ Tetracycline - pharmacology
/ Tetracycline-responsive
/ Trans-Activators - drug effects
/ Transgenes
/ Transgenic animals
/ Transgenic mice
2018
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A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression
by
Murach, Kevin A.
, Wen, Yuan
, Englund, Davis A.
, Mobley, Christopher B.
, Dungan, Cory M.
, McCarthy, John J.
, Vechetti, Ivan J.
, Iwata, Masahiro
, Peterson, Charlotte A.
in
Actin
/ Animals
/ Antibiotics
/ Biochemistry
/ Biomedical and Life Sciences
/ Biotechnology
/ Cell Biology
/ Cloning
/ Developmental Biology
/ Fluorescence
/ Gene expression
/ Gene Targeting - methods
/ Genes
/ Genetic engineering
/ Green fluorescent protein
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Histone H2B
/ Humans
/ Immunohistochemistry
/ Kinases
/ Life Sciences
/ Methodology
/ Mice
/ Mice, Inbred C57BL
/ Muscle proteins
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscles
/ Musculoskeletal system
/ PAX7 Transcription Factor - genetics
/ PAX7 Transcription Factor - metabolism
/ Reverse transcription
/ RNA
/ Rodents
/ Satellite cells
/ Skeletal muscle
/ Skeletal muscle-specific
/ Systems Biology
/ Tetracycline - pharmacology
/ Tetracycline-responsive
/ Trans-Activators - drug effects
/ Transgenes
/ Transgenic animals
/ Transgenic mice
2018
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A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression
by
Murach, Kevin A.
, Wen, Yuan
, Englund, Davis A.
, Mobley, Christopher B.
, Dungan, Cory M.
, McCarthy, John J.
, Vechetti, Ivan J.
, Iwata, Masahiro
, Peterson, Charlotte A.
in
Actin
/ Animals
/ Antibiotics
/ Biochemistry
/ Biomedical and Life Sciences
/ Biotechnology
/ Cell Biology
/ Cloning
/ Developmental Biology
/ Fluorescence
/ Gene expression
/ Gene Targeting - methods
/ Genes
/ Genetic engineering
/ Green fluorescent protein
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Histone H2B
/ Humans
/ Immunohistochemistry
/ Kinases
/ Life Sciences
/ Methodology
/ Mice
/ Mice, Inbred C57BL
/ Muscle proteins
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscles
/ Musculoskeletal system
/ PAX7 Transcription Factor - genetics
/ PAX7 Transcription Factor - metabolism
/ Reverse transcription
/ RNA
/ Rodents
/ Satellite cells
/ Skeletal muscle
/ Skeletal muscle-specific
/ Systems Biology
/ Tetracycline - pharmacology
/ Tetracycline-responsive
/ Trans-Activators - drug effects
/ Transgenes
/ Transgenic animals
/ Transgenic mice
2018
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A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression
Journal Article
A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression
2018
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Overview
Background
The tetracycline-responsive system (Tet-ON/OFF) has proven to be a valuable tool for manipulating gene expression in an inducible, temporal, and tissue-specific manner. The purpose of this study was to create and characterize a new transgenic mouse strain utilizing the human skeletal muscle α-actin (HSA) promoter to drive skeletal muscle-specific expression of the reverse tetracycline transactivator (rtTA) gene which we have designated as the HSA-rtTA mouse.
Methods
To confirm the HSA-rtTA mouse was capable of driving skeletal muscle-specific expression, we crossed the HSA-rtTA mouse with the tetracycline-responsive histone H2B-green fluorescent protein (H2B-GFP) transgenic mouse in order to label myonuclei.
Results
Reverse transcription-PCR confirmed skeletal muscle-specific expression of rtTA mRNA, while single-fiber analysis showed highly effective GFP labeling of myonuclei in both fast- and slow-twitch skeletal muscles. Pax7 immunohistochemistry of skeletal muscle cross-sections revealed no appreciable GFP expression in satellite cells.
Conclusions
The HSA-rtTA transgenic mouse allows for robust, specific, and inducible gene expression across muscles of different fiber types. The HSA-rtTA mouse provides a powerful tool to manipulate gene expression in skeletal muscle.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Animals
/ Biomedical and Life Sciences
/ Cloning
/ Genes
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Humans
/ Kinases
/ Mice
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscles
/ PAX7 Transcription Factor - genetics
/ PAX7 Transcription Factor - metabolism
/ RNA
/ Rodents
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