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Telopeptide intact rat tail collagen

Manufactured by Advanced BioMatrix

Telopeptide-intact rat tail collagen is a laboratory product that provides a source of native, unmodified Type I collagen. It is extracted from the rat tail tendon and retains the natural telopeptide regions of the collagen molecule. This collagen can be used in various cell culture and tissue engineering applications that require a physiologically relevant extracellular matrix component.

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2 protocols using telopeptide intact rat tail collagen

1

Collagen Gel Preparation and Cell Seeding

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Atelopeptide fibrillar bovine dermal collagen (no. 5005-B; PureCol, Advanced BioMatrix) was prepared at 1.7 mg ml−1 in DMEM: 100 μl per well in 96-well plates; 300 μl per well in 24-well plates, 700 μl per well in 12-well plates. Telopeptide-intact rat tail collagen (no. 5153-A; PureCol, Advanced BioMatrix) was prepared at 0.5 mg ml −1 following the manufacturer’s instructions (700 μl per well in 24-well plates). Bovine collagen gels at 1.7 mg ml−1 and rat tail collagen gels at 0.5 mg ml−1 have comparable stiffness, pore diameter and pore cross section as previously described22 (link). After collagen gel polymerization (4 h for bovine collagen, 2 h for rat tail collagen), cells were seeded on top of collagen in medium containing 10% FCS, allowed to adhere for 24 h and medium changed to 1% serum for 24 h. Except where indicated, imaging and immunoblotting were performed on cells cultured on a thick layer of collagen I.
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2

Collagen Gel Preparation and Cell Seeding

Check if the same lab product or an alternative is used in the 5 most similar protocols
Atelopeptide fibrillar bovine dermal collagen (no. 5005-B; PureCol, Advanced BioMatrix) was prepared at 1.7 mg ml−1 in DMEM: 100 μl per well in 96-well plates; 300 μl per well in 24-well plates, 700 μl per well in 12-well plates. Telopeptide-intact rat tail collagen (no. 5153-A; PureCol, Advanced BioMatrix) was prepared at 0.5 mg ml −1 following the manufacturer’s instructions (700 μl per well in 24-well plates). Bovine collagen gels at 1.7 mg ml−1 and rat tail collagen gels at 0.5 mg ml−1 have comparable stiffness, pore diameter and pore cross section as previously described22 (link). After collagen gel polymerization (4 h for bovine collagen, 2 h for rat tail collagen), cells were seeded on top of collagen in medium containing 10% FCS, allowed to adhere for 24 h and medium changed to 1% serum for 24 h. Except where indicated, imaging and immunoblotting were performed on cells cultured on a thick layer of collagen I.
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