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L6 glut4myc cells

Manufactured by Kerafast
Sourced in United States

L6-GLUT4myc cells are a cell line derived from rat skeletal muscle that stably expresses the GLUT4 glucose transporter with a c-Myc tag. These cells can be used to study glucose uptake and the trafficking of GLUT4 in response to insulin or other stimuli.

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2 protocols using l6 glut4myc cells

1

Generating mtDNA-depleted L6-GLUT4myc cell line

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L6-GLUT4myc cells, a L6 skeletal muscle cell line (Kerafast, Inc., Boston, MA, USA), were harvested in α-MEM supplemented with a 10% FBS and 1% penicillin-streptomycin solution according to a previous study [12 (link)]. As prolonged exposure to low concentrations of EtBr inhibits the replication of mtDNA selectively, a L6-GLUT4myc cell line depleted of mtDNA was prepared by incubating the cells with EtBr (0.2 µg/ml) and uridine (50 µg/ml) for 3 weeks. The reversal of mtDNA depletion was achieved within 7 days by the removal of EtBr and uridine. The control cells were cultured for the same time period under normal harvesting conditions.
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2

L6-GLUT4myc Cell Line Protocol

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Materials: The rat L6 muscle cell line, stably expressing myc-tagged GLUT4 (L6-GLUT4myc cells), was obtained from Kerafast (Boston, MA, USA). Fetal bovine serum, modified Eagle’s medium (α-MEM), standard culture medium, and all other tissue culture reagents were purchased from Biological Industries (Beit Haemek, Israel). Horseradish peroxidase (HRP)-conjugated goat anti-rabbit antibodies were obtained from Promega (Madison, WI, USA). Polyclonal anti-myc (A-14); the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) reagent; methoxyamine hydrochloride; pyridine; N-methyl-N-(trimethylsilyl)-trifluoroacetamide (MSTFA); and other standard chemicals were purchased from Sigma Aldrich (St. Louis, MO, USA).
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