Mechano-mimetic cell culture.
Traction Force Microscopy.
Cell-contractile forces generated by the actomyosin cytoskeleton and transmitted to the extracellular matrix (ECM) drive cell adhesion, spreading, and migration. These forces are known to be critical during embryo morphogenesis, wound healing, immune response as well as pathological processes, such as cancer metastasis. Traction force microscopy (TFM) is a recognized experimental technique that measures the surface forces, also termed as tractions, that cells exert on a substrate. It relies on the computational analysis of the direction and the magnitude of elastic substrate deformations to reconstruct cell-generated traction forces. These deformations can be tracked and quantified by recording the displacement of fluorescent beads embedded in the substrate, as a result of the mechanical stress induced by an adherent cell.
DESCRIPTION
Polyacrylamide gel with fluorescent carboxylate-modified microspheres uniformly dispersed inside.
APPLICATIONS
Traction Force Microscopy.
CHARACTERISTICS
BENEFITS | Relevant, robust, reliable, plug & play, compliant, disruptive, no biological risk (synthetic matrix), glass bottom: ideal for microscopy, stiffness and coating are decoupled.
STORAGE | Temperature: +4°C. Shelf life: 3 months.
BEADS* | Size: 0.2 µm. Fluorophore: dark red. Wavelength: Exit. / Emiss. ; 660 / 680 nm. Cell seeding surface: 6.15 cm².
*Specific beads on request
CUSTOMIZATION
1
CHOOSE YOUR STIFFNESS
Standards stiffnesses:
8 kPa
10 kPa
12 kPa
*Specifics stiffnesses on request
Culture dishes and plates are pre-coated with ECM protein or synthetic amino acid. Culture dedicated surface chemistry:
2
CHOOSE YOUR COATING
Vitronectin
Human; recombinant truncated
Human; plasma
Fibronectin
Collagen I
Rat; tail
Laminin
Mouse; EHC sarcoma
Poly-Ornithine | Laminin
Poly-Ornithine
Uniform rigidity:
3
UNIQUE
PD35
FORMAT
Rigidity step: