Luciferase Stable PC3 Cell Line
|T3006||1x106 cells / 1.0 ml|
Luciferase is commonly used as a reporter to assess the transcriptional activity of a genetic construct with luciferase gene under the promoter of interest. The Luciferase stable PC3 Cell line was generated using abm's LV010087 on PC3 cells. The expression of luciferase has been confirmed with luciferase assay. All clones are puromycin (0.1µg/ml)-resistant. Luciferase stable PC3 cells can be a very useful cell line for non-invasive visualization in in vitro experiments.
|Species||Human (H. sapiens)|
|Species description||Homo sapiens|
|Seeding Density||40,000 - 60,000 cells/cm2; Recommended split ratio is 1:2 to 1:3|
|Population Doubling Time||45 - 52 hours|
For Research Use Only
|Unit quantity||1x106 cells / 1.0 ml|
Induced with lentivirus containing the LUCIFERASE (LUC2) Lentiviral Vector (Photinus pyralis) (UbC), Cat. No. LV010087
|Caution||For Research Use Only|
|Clone Name||13, 38|
|Cell Type||Reporter Cells|
Use of PriCoatTMT25 Flasks (G299) or Applied Cell Extracellular Matrix (G422) is required for cell adhesion to the culture vessels. Grow cells inECM-coated culture vessels unless otherwise specified in the Propagation Requirements below.
The base medium for this cell line is Prigrow IV medium available at abm, Cat. No. TM004. 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 Solution (G255) to a final concentration of 1%. 0.1µg/ml of Puromycin (G264) may be added for selection.
1. For for-profit organizations and corporations, please contact [email protected] for pricing of this item.
2. Sale of this item is subjected to the completion of a Material Transfer Agreement (MTA) by the purchasing individual/institution for each order. If you have any questions regarding this, please contact us at [email protected].
3. 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 or ordering RNA (0.5 μg, Cat.# C207, $450.00) or cell lysate (100 μg, Cat.# C206, $600.00) to perform preliminary experiments, or alternatively use our Gene Expression Assay Service (Cat# C138). All sales are final.
4. We 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 evaluate the feasibility of live cell shipment by taking into account the final destination's temperature variation and its geographical location. 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).
5. 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.
6. 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.
7. abm warrants that cell lines shall be viable upon initiation of culture for a period of thirty (30) days after shipment and that they shall meet the specifications on the applicable abm Material Product Information sheet, certificate of analysis, and/or catalog description. Such thirty (30) day period is referred to herein as the "Warranty Period."
|Do you have a protocol for imaging when the cells are in animals?|
At present, we do not have any further information to support this application. We apologize for any inconvenience.
|What is the selection marker for this cell line?|
The selection marker is puromycin.
|Which luciferase gene is used in the production of this cell line, and what promoter is driving its expression?|
This cell line contains firefly luciferase (Photinus pyralis), driven by a UbC promoter
|Is the GFP or RFP signal localized within the cell?|
|What type of GFP or RFP do these cell lines express, and from which promoter?|
The GFP is derived from copGFP (from Pontellina plumata) and the RFP is derived from mKate2 (from Entacmaea quadricolor). They are expressed from a proximal SV40 promoter, and a more distal CMV promoter may also drive expression. If you are looking for a cell line with a specific fluorescent reporter, or with a specific promoter, abm can perform a Stable Cell Line Generation service. Simply ask [email protected] for a quote.
- Deep, G. et al. "Silibinin inhibits fibronectin induced motility, invasiveness and survival in human prostate carcinoma PC3 cells via targeting integrin signaling" Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 768:35-46 (2014). PubMed: 25285031.
- Schlaepfer, I. R et al. "Inhibition of Lipid Oxidation Increases Glucose Metabolism and Enhances 2-Deoxy-2-[18F]Fluoro-d-Glucose Uptake in Prostate Cancer Mouse Xenografts" Molecular Imaging and Biology 4:529-538 (2015). DOI: 10.1007/s11307-014-0814-4.
- Chatterjee, A et al. "The Addition of Manganese Porphyrins during Radiation Inhibits Prostate Cancer Growth and Simultaneously Protects Normal Prostate Tissue from Radiation Damage" Antioxidants (Basel). 7(1):21 (2018). DOI: 10.3390/antiox7010021.