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Atelopeptide fibrillar bovine dermal collagen

Manufactured by Advanced BioMatrix

Atelopeptide fibrillar bovine dermal collagen is a type of lab equipment used for research and development purposes. It is derived from bovine (cow) skin and is characterized by the absence of telopeptides, which are the non-helical regions of the collagen molecule. This product maintains the natural fibrillar structure of collagen.

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2 protocols using atelopeptide fibrillar bovine dermal 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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