Overview
- Species: Human
- Additional Attributes: 3D Hydrogels, Collagen, Extracellular Matrix
- Specific Attributes: Telocollagen/acidic treatment, Type I
- Features:3 mg/ml
VitroCol®, Human Collagen, Solution
Cat.-Nr.: 5007-20ML
Description
VitroCol® collagen is the first widely available, naturally produced purified human collagen for research purposes. VitroCol® sets the standard for purity (>99% collagen content), functionality and represents the only native-like human collagen offered.
VitroCol® collagen is naturally secreted from human neo-natal fibroblast cells. The human fibroblasts are cultured in optimal conditions allowing the fibroblast to naturally and efficiently secret extracellular matrix. The extracellular matrix is then processed and purified to yield the naturally produced human collagen.
VitroCol® is approximately 97% Type I human collagen with the remainder being comprised of Type III collagen. VitroCol® is supplied at approximately 3 mg/ml concentration. The concentration for each specific lot is provided on a Certificate of Analysis that is available with the purchase of each product. VitroCol® is soluble atelocollagen in 0.01 N HCI, therefore, the pH is 2.
VitroCol® is especially ideal for human cell culture systems when coating of surfaces, providing preparations of thin layers of culturing cells, or use as a solid gel. VitroCol® human collagen is provided in user-friendly packaging for use and storage. VitroCol® is sterile filtered and is supplied as a ready to use solution.
For extensive users of this product: The VitroCol® collagen is available in a 100 ml unit, too. (please contact us)
For an overview of Type I Collagen (Atelocollagen & Telocollagen) products (click)
SUPPLIER:
Advanced BioMatrix
STATUS:
In Stock
SIZE:
20 ml
References
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- Sabbione, Florencia, et al. "Neutrophil extracellular traps stimulate proinflammatory responses in human airway epithelial cells." Journal of innate immunity 9.4 (2017): 387-402.
- Dos Santos Brilha, S., et al. "Monocyte adhesion, migration and extracellular matrix breakdown is regulated by integrin αVβ3 in Mycobacterium tuberculosis infection."
- Brilha, Sara, et al. "Monocyte Adhesion, Migration, and Extracellular Matrix Breakdown Is Regulated by Integrin aVb3 in Mycobacterium tuberculosis Infection." (2017).
- Colace, T., et al. "Analysis of morphology of platelet aggregates formed on collagen under laminar blood flow." Annals of biomedical engineering 39.2 (2011): 922-929.
- Muthard, Ryan W., and Scott L. Diamond. "Blood clots are rapidly assembled hemodynamic sensors: flow arrest triggers intraluminal thrombus contraction." Arteriosclerosis, thrombosis, and vascular biology 32.12 (2012): 2938-2945.
- Maloney, S. F., Lawrence F. Brass, and S. L. Diamond. "P2Y12 or P2Y1inhibitors reduce platelet deposition in a microfluidic model of thrombosis while apyrase lacks efficacy under flow conditions." Integrative Biology 2.4 (2010): 183-192.
- Bauer, Rebecca N., et al. "Interaction with epithelial cells modifies airway macrophage response to ozone." American journal of respiratory cell and molecular biology 52.3 (2015): 285-294.
- Kawamura, Shunsuke, et al. "Identification of common monocyte progenitors, pre-monocytes, and granulocyte monocyte progenitors in human umbilical cord blood." Experimental Hematology 43.9 (2015): S72.
HIS – Hepatocyte Isolation System