Cat. #161147
MDA-MB-231/EGFP_Cytochrome c
Cat. #: 161147
Availability: 8-10 weeks
Organism: Human
Tissue: Breast
Disease: Cancer
Model: Transgenic
£575.00
This fee is applicable only for non-profit organisations. If you are a for-profit organisation or a researcher working on commercially-sponsored academic research, you will need to contact our licensing team for a commercial use license.
Contributor
Inventor: T.R. Santhosh Kumar
Institute: Rajiv Gandhi Centre for Biotechnology
Primary Citation: Srinivas KP, et.al. PMID:26992219
Tool Details
*FOR RESEARCH USE ONLY (for other uses, please contact the licensing team)
- Name: MDA-MB-231/EGFP_Cytochrome c
- Cancer: Breast cancer
- Cancers detailed: Breast cancer
- Research fields: Cancer;Disease (not cancer);Metabolism
- Parental cell: MDA-MB-231
- Organism: Human
- Gender: Female
- Tissue: Breast
- Disease: Cancer
- Morphology: Epithelial
- Growth properties: Adherent
- Model: Transgenic
- Crispr: No
- Conditional: No
- Description: The product is a human cervical carcinoma cell line MDA-MB-231, transfected to stably express the protein cytochrome c (cyt-c) tagged with EGFP. The EGFP-tag enables easy identification of the cyt-c release in live cells upon apoptotic induction. The cell line can be utilized for studying the apoptosis process and to screen of potential candidate drugs that induce apoptosis.
Handling
- Growth medium: DMEM with 2mM L-Glutamine and 10% FBS (Heat inactivated), or Leibovitz's L15 with 2mM L-Glutamine and 10% Fetal Bovine serum.
- Temperature: 37° C
- Atmosphere: 5% CO2
- Shipping conditions: Dry Ice
- Storage medium: Growth medium + 10% DMSO
- Storage conditions: Liquid Nitrogen
- Initial handling information: Resuscitation: Rapidly thaw the frozen ampoule in a water bath at 37?°C for 1-2 minutes. Transfer the contents to a centrifuge tube and slowly add 5-10ml of pre-warmed growth media. Remove a sample for counting. Centrifuge at 100-150g for 2-3 minutes to pellet cells (a centrifugation step to remove the cryoprotectant is essential. Seed at the recommend density, e.g. greater than 10,000 cells per cm2.
- Subculture routine: Subculture non-confluent cultures using trypsin/EDTA and 1:3 to 1:4, i.e. seeding at 1-4 x10,000 cells/cm? .
- Cultured in antibiotics: No
References
- Srinivas KP, et.al. PMID:26992219