5074
PureCol™ EZ Gel solution
Synonyme(s) :
Collagen type
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About This Item
Code UNSPSC :
12352202
Nomenclature NACRES :
NA.75
Produits recommandés
Source biologique
bovine skin
Niveau de qualité
Stérilité
sterile
Pureté
≥99% (SDS-PAGE Electrophoresis – Silver Stain, SDS-PAGE)
Forme
solid
Conditionnement
pkg of 35 mL
Technique(s)
cell culture | mammalian: suitable
Conditions d'expédition
wet ice
Température de stockage
2-8°C
Catégories apparentées
Description générale
PureCol™ is used in cell culture, tissue engineering and as a coating material for medical devices.PureCol EZ Gel is a ready-to-use collagen solution that forms a firm gel by simply warming to 37°C in an incubator. The product consists of purified Type I bovine collagen at a concentration of approximately 5 mg/ml (0.5%), DMEM/F-12 medium and a mixture of L-glutamine and dipeptide (L-alanine-L-glutamine) to provide a long-lasting L-glutamine source for cell culture.
Application
The PureCol™ EZ Gel solution has been used:
- for coating culture plates to facilitate the seeding and growth of epithelial cells derived from human nasal epithelial tissue
- as a component in the bioartificial tendon preparation, providing a gel matrix for seeding human tendon cells and promoting their growth and collagen gel formation
- for embedding mouse Achilles tendon-derived cells in 3D-collagen constructs, providing a biomimetic environment for studying tendon biology and performing qPCR, immunohistochemical, and western blot analyses.
Caractéristiques et avantages
PureCol EZ Gel is designed to improve gel consistency by providing a pre-formulated solution of media and collagen that have been adjusted to a neutral pH. This product avoids the inconsistencies in the preparation of the gel that can arise through variables of reagent addition, pH adjustment and handling conditions. PureCol EZ Gel is ideal for providing a firm gel and can also be used in the preparation of a thin layer for culturing cells. PureCol EZ Gel collagen is provided in a user-friendly packaging for use and storage. This product is sterile and supplied as a ready to use solution. PureCol EZ Gel is available in 35 mL volume, and produced by aseptic processing. 3D gels allow for the study of the effects of the mechanical properties of the ECM, such as density and rigidity, on cell development, migration, and morphology. Unlike 2D systems, 3D environments allow cell extensions to simultaneously interact with integrins on all cell surfaces, resulting in the activation of specific signaling pathways. Gel stiffness or rigidity also affects cell migration differently in 3D versus 2D environments. Furthermore, integrin-independent mechanical interactions resulting from the entanglement of matrix fibrils with cell extensions are possible in 3D systems, but not in 2D systems where the cells are attached to a flat surface.1-3
Notes préparatoires
3-D Gel Preparation Procedure
1. Remove PureCol EZ Gel from 2-10°C storage. To prevent gelation, maintain temperature of product at 2-10°C.
2. Introduce PureCol EZ Gel into cell culture system. Cells can be added to the PureCol EZ Gel solution.
3. To form gel, warm to 37°C. The beginning of gelation will occur within 40 minutes, but allow approximately 90 to minutes for firm gel formation.
1. Remove PureCol EZ Gel from 2-10°C storage. To prevent gelation, maintain temperature of product at 2-10°C.
2. Introduce PureCol EZ Gel into cell culture system. Cells can be added to the PureCol EZ Gel solution.
3. To form gel, warm to 37°C. The beginning of gelation will occur within 40 minutes, but allow approximately 90 to minutes for firm gel formation.
Informations légales
PureCol is a trademark of Advanced BioMatrix, Inc.
Code de la classe de stockage
13 - Non Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Les clients ont également consulté
Muhammad H Zaman et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(29), 10889-10894 (2006-07-13)
Cell migration on 2D surfaces is governed by a balance between counteracting tractile and adhesion forces. Although biochemical factors such as adhesion receptor and ligand concentration and binding, signaling through cell adhesion complexes, and cytoskeletal structure assembly/disassembly have been studied
Karen A Beningo et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(52), 18024-18029 (2004-12-17)
Fibroblasts in 2D cultures differ dramatically in behavior from those in the 3D environment of a multicellular organism. However, the basis of this disparity is unknown. A key difference is the spatial arrangement of anchored extracellular matrix (ECM) receptors to
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Molecular biology of the cell, 16(11), 5070-5076 (2005-08-19)
Fibroblast-3D collagen matrix culture provides a physiologically relevant model to study cell-matrix interactions. In tissues, fibroblasts are phagocytic cells, and in culture, they have been shown to ingest both fibronectin and collagen-coated latex particles. Compared with cells on collagen-coated coverslips
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