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BMP Responsive Immortalized Reporter (BRITER) Cell Line

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BMP Responsive Immortalized Reporter (BRITER) Cell Line

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BMP Responsive Immortalized Reporter (BRITER) Cell Line

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	Print Version
Biosesafety Level	II
Organism	Bmp2^c/c;Bmp4^c/c; R26CreER Neonatal Mouse
SourceOrgan	Calvariae
Growth Properties	Adherent
Morphology	Multipolar
Description	Bone morphogenetic proteins (BMPs) are useful as therapeutic agents to promote the regeneration of bone at the site of trauma following bone fracture, spinal injury or surgery but are limited due to systemic-wide side effects, the necessity of specialized delivery systems, and the short half lives of the compounds in vivo. The BMP Responsive Immortalized Reporter (BRITER) Cell Line was generated in order to conduct high-thoroughput chemical and molecular genetic screening to identify a novel small molecule alternative activator of BMP signaling. The cells are immortalized tamoxifen inducible Bmp2; Bmp4 double conditional knockout murine calvarial osteoblast cells expressing a BMP Response Element(BRE)-dependent Firefly Luciferase (FFLuc) gene and an SV40 promoter/enhancer-dependent Renilla Luciferase (RRLuc) gene. FFLuc activity increases in response to BMP signaling activity while the RRLuc gene acts as an internal control to limit the number of false-positives resulting from non-specific activation of cellular processes, such as cell proliferation. In addition the sensitivity to exogenous BMP signaling can be intensified through the addition of 4-hydroxytamoxifen, which reduces the level of endogenous BMP signaling through the knockout of the Bmp2 and Bmp4 genes resulting in a specific and highly efficient reporter of BRE activation.
Procedure Overview
Recommended Seeding Density	Thaw entire contents into an appropriate T25 flask as specified in the Propagation instructions.
Markers	Osterix, CollA1, BSP, Runx, Osteocalcin, Alkaline phosphatase
Applications	For Research Use Only
Propagation	Use of PriCoat™ T25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) is required for cell adhesion to the culture vessels. Grow cells in ECM-coated culture vessels with the following conditions. The base medium for this cell line is Prigrow III medium available in ABM, Cat. No. TM003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (TM999) to a final concentration of 10% and Penicillin/Streptomycin(G255). Atmosphere: air, 95%; Carbon dioxide (CO₂), 5%. Temperature: 37.0°C.
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Disclaimer	1. The CoA for this product (provided upon request) verifies the cell-type specific gene expression via RT-PCR only. All test parameters provided in the CoA are conducted using abm's standardized culture system and procedures. The stated values may vary under the end-user's culture conditions. Please verify that the product is suitable for your studies by referencing published papers. All sales are final. 2. We strongly recommend live cell shipments for ease of cell transfer and this option can be requested at the time of ordering. Please note that the end-user will need to evalsuate the feasibility of live cell shipment by taking into account the final destination's temperature variation and its geographical locations. In addition, we thoroughly test our cell lines for freeze-thaw recovery. If frozen cells were received and not recovered in your lab under the exact, specified conditions (using recommended culture vessel, media, additional supplements, and atmospheric conditions), a live cell replacement is possible at a cost (plus shipping). 3. All of abm's cell biology products are for research use ONLY and NOT for therapeutic/diagnostic applications. abm is not liable for any repercussions arising from the use of its cell biology product(s) in therapeutic/diagnostic application(s). Please contact a technical service representative for more information. 4. abm makes no warranties or representations as to the accuracy of the information on this site. Citations from literature and provided for informational purposes only. abm does not warrant that such information has been shown to be accurate.