#162201

SW480 EGFP-emerin cell line clone 2

Cat. #162201

SW480 EGFP-emerin cell line clone 2

Cat. #: 162201

Organism: Human

Tissue: Colon

Model: Genetically modified cell line

£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: Stefan Przyborski

Institute: University of Durham

Tool Details
Target Details
Handling
References

Tool Details

*FOR RESEARCH USE ONLY (for other uses, please contact the licensing team)

  • Name: SW480 EGFP-emerin cell line clone 2
  • Alternate name: SW480 GFP-emerin 2;
  • Parental cell: SW480
  • Clone: clone 2
  • Organism: Human
  • Tissue: Colon
  • Morphology: Epithelial
  • Growth properties: Adherent
  • Model: Genetically modified cell line
  • Receptors of note: No
  • Description: Colon cancer cell line stably transfected with EGFP-emerin. Suitable for studying the effect of the presence of lamin and/or emerin on cancer cell properties.
  • Recommended controls: Same cell line stably transfected with EGFP not tagged to any other DNA

Target Details

  • Target: Emerin
  • Target background: Class II nuclear protein integral to the inner nucleear membrane which binds lamin A/C.

Handling

  • Format: Frozen
  • Passage number: Not known. Cells are high passage (>100) due to being a cancer cell line from a culture bank and then going through multiple passages to grow up the stable transfectants.
  • Growth medium: L15 (Leibovitz) medium with 2mM L-Glutamine, 10% FBS and 100units/ml penicillin / 100ug/ml streptomycin
  • Atmosphere: Without CO2
  • Shipping conditions: Dry ice
  • Storage medium: L15 (Leibovitz) medium with 2mM L-Glutamine, 10% FBS and 10% DMSO
  • Storage conditions: Liquid Nitrogen
  • Initial handling information: Continue to store at ?-70deg C. To bring up cells, defrost quickly in 37?C water bath and seed in petri dish/flask. Once cells have adhered to culture surface, change media to DMSO-free media.
  • Subculture routine: Passage at 70-80% confluencey in the presence of 0.25% trypsin in 0.5mM EDTA/PBS. Incubate at 37?C, 5% Co2, humidified for 2 minutes. Split 1:4.
  • Cultured in antibiotics: penicillin/streptomycin
  • Characterisation tests: RT-PCR, IF and Western Blotting to confirm expression of lamin A
  • Str profiling: Unpublished WB analysis available

References

  • Unpublished