Catalogue | DB_003

Porcine Immortalised Myosatellite Cells

This piMyoSat line is an immortalised cell line with a rapid population doubling and differentiation protocol time, piMyoSat’s will strengthen and accelerate your discovery work, and are suitable for use in cultivated muscle production.

Porcine Immortalised Myosatellite Cells
Consistent

Consistent

Homogenous myogenic cell population creates a stable model for foundational and applied research

Easy to Use

Easy to Use

Simple to follow expansion and differentiation protocols.

Quick

Quick

Rapidly form striated myocytes in days to accelerate your R&D

Porcine Immortalised Myosatellite Cells
Dragon Biotechnologies
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Cell Characterization

piMyoSat growth data. Top) representative image of piMyoSats and positive expression for the SV40T antigen. Bottom) Representative cell growth curve over 5 days of culture.

Following enzymatic digestion of fresh porcine abdominal skeletal muscle tissue, cells were cultured on treated cell culture plastic to deplete cell suspensions of fibroblasts after which they were transferred onto type I collagen coated surfaces to select for myosatellite cells. Cultures were maintained for 2 passages to expand the myosatellite population. Myosatellite cells were immortalised by incubation with Lentivirus containing the SV40 large T antigen for 24 hours. Immortalised cells were selected by treatment of cultures with neomycin for 7 days. Lentiviral vectors are integrative so the expression of the SV40 large T antigen is constitutive. The SV40 large T antigen suppresses the expression of the cell cycle regulator P53 locking cells in the cell cycle. piMyoSats test positive for the expression of the SV40 large T antigen and negative for residual Lentivirus. Following immortalisation piMyoSats retain their capacity for myogenic differentiation. piMyoSats are cultured on type I collagen coated surfaces in high glucose DMEM containing 10% FBS.

Differentiation Characterization

Differentiation of piMyoSats to skeletal muscle. Top) Staining of multinucleated fibres and flow cytometry for the differentiation markers myogenin and PAX7. Bottom) gene expression of the markers PAX7, MYH4, MYOD1, MYF5, MYOG and DES over the course of differentiation.

Compatible Processes

Cell Growth Formats
Adherent
Cell Culture Vessels
Well Plates
Flasks

Product information

12-18 hours
Avg. Population Doubling Time
Skeletal Muscle Differentiation
0 days
10 days
Immortalisation Method
Lentiviral SV40 large T antigen
Species (Latin)
Sus scrofa domesticus
Founder Animal
Male, Duroc white
Working Cell Bank Passage Number
P3-P10
Maximum Passage Number Achieved
P20
Quality Control
Sterility and mycoplasma testing
Format

Cryopreserved cells, one vial containing 1x106 cells

User Storage
-150°C or LN2
Shipping Method
Dry ice for immediate ultra-cold storage