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The plasmid solution (1 µg of each plasmid in 20 µl of PBS) was injected i.m. along the fibres into the TC muscle using an 29G insulin syringe.
When the same investigators measured protein synthesis in the epitrochlearis muscle using an in vitro technique they found no difference between dexamethasone-treated and pair-fed animals [1], [2].
RNA was extracted from muscle using an E.Z.N.A. Tissue RNA kit (Omega Bio-Tek, Inc., Norcross, GA) according to the manufacturer's protocol using Precellys Ceramic Homogenisation beads (CK14, PEQLAB Ltd ,Farnborough, UK) and a Hybaid Ribolyser (Thermo Scientific, Loughborough, United Kingdom).
Transcriptomic analysis was performed in mid intestine, liver and skeletal muscle, using an Atlantic salmon oligonucleotide microarray (Salar_2, Agilent 4x44K).
Williams in 1996 reported several animal experiments on limb and facial muscle using an implantable electrical stimulator [ 73, 74].
Total RNA was purified from crushed, frozen muscle using an RNeasy Mini Kit (QIAgen) according to the manufacturer's specifications.
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These nanoparticles were injected into gastrocnemius muscles (20 µl per muscle) using a 35 g WPI NanoFil syringe.
This article focuses on establishing communication between a functional muscle and a denervated muscle using a radiofrequency communications link.
The aim of the present study was to investigate the effect of celandine on the uterine muscle, using a perfusion model of swine uteri.
Pre-fabrication of AChR clusters on engineered skeletal muscle using a released neurotrophic factor can accelerate innervations following implantation in vivo.
After skin incision, the subplatysmal skin flap is elevated just above the sternocleidomastoid (SCM) muscle using a monopolar electrocautery under direct vision.
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CEO of Professional Science Editing for Scientists @ prosciediting.com