KC-1496

HEK293-ERBB3-Cell-Line

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Background of HEK293-ERBB3-Cell-Line

ERBB3, also known as HER3, is a transmembrane protein belonging to epidermal growth factor receptor (ERBB) family of receptor tyrosine kinase. The kinase domain impaired ERBB3 can from active heterodimer with other member of ERBB family, this heterodimer, mostly with ERBB2 after binding with its ligand NRG1 or NRG2, play an important role in cancer growth, invasion, metastasis and chemotherapeutic resistant.

Specifications

Catalog NumberKC-1496
Cell Line NameHEK293-ERBB3-Cell-Line
Host Cell LineHEK293
DescriptionStable HEK293 cell line expressing exogenous human ERBB3 gene
QuantityTwo vials of frozen cells (≥2-106/vial)
StabilityStable in culture over a minimum of 10 passages
ApplicationDrug screening and biological assays
Freezing Medium70% DMEM + 20% FBS + 10% DMSO
Propagation MediumDMEM + 10% FBS + 1μg/ml Puromycin
Selection MarkerPuromycin
MorphologyFibroblastoid cells growing as a monolayer
SubcultureSplit saturated culture 1:4-1:5 every 2-3 days; seed out at about 1-3 × 105 cells/ml
Incubation37 °C with 5% CO2
StorageLiquid nitrogen immediately upon receiving
Doubling TimeApproximately 30 hours
Mycoplasma StatusNegative
In Vivo ValidationNA

Cell Line Generation

HEK293 human ERBB3 cell line was generated using a lentiviral vector expressing the human ERBB3 sequence.

Characterization

Figure: Characterization of ERBB3 overexpression in HEK293 stable clones using FACS.

Cell Resuscitation

  1. Prewarm culture medium (DMEM supplemented with 10% FBS and 1μg/mL Puromycin)in a 37°C water bath.
  2. Thaw the frozen vial in a 37°C water bath for 1-2 minutes.
  3. Transfer the vial into biosafety cabinet, and wipe the surface with 70% ethanol.
  4. Unscrew the top of the vial and transfer the cell suspension gently into a sterile centrifuge tube containing 9.0mL complete culture medium.
  5. Spin at ~ 125 × g for 5-7 minutes at room temperature, and discard the supernatant without disturbing the pellet.
  6. Resuspend cell pellet with the appropriate volume of complete medium and transfer the cell suspension into a T25 culture flask.
  7. Incubate the flask at 37°C, 5% CO2 incubator.
  8. Split saturated culture 1:4-1:5 every 2-3 days; seed out at about 1-3 × 105 cells/mL.

Cell Freezing

  1. Prepare the freezing medium (70% DMEM + 20% FBS + 10% DMSO) fresh immediately before use.
  2. Keep the freezing medium on ice and label cryovials.
  3. Transfer cells to a sterile, conical centrifuge tube, and count the cells.
  4. Centrifuge the cells at 250×g for 5 minutes at room temperature and carefully aspirate off the medium.
  5. Resuspend the cells at a density of at least 3×106 cells/mL in chilled freezing medium.
  6. Aliquot 1 mL of the cell suspension into each cryovial.
  7. Freeze cells in the CoolCell freezing container overnight in a -80°C freezer.
  8. Transfer vials to liquid nitrogen for long-term storage

References

  1. Jaiswal, B. S. et al. Oncogenic ERBB3 Mutations in Human Cancers. Cancer Cell 23, 603–617 (2013).
  2. Baselga, J. & Swain, S. M. Novel anticancer targets: Revisiting ERBB2 and discovering ERBB3. Nat. Rev. Cancer 9,
  3. 463–475 (2009).
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