KC-3193

CHOK1-CDH6-Cell-Line

Stable CHOK1 cell line expressing exogenous human CDH6 gene

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Background of CHOK1-CDH6-Cell-Line

CDH6, also known as CAD6, is a type II classical cadherin that belongs to the cadherin superfamily. CDH6 has high expressions in kidney, brain, and cerebellum, and low expressions in lung, pancreas, gastric mucosa, and cytotrophoblasts. CDH6 is also found in renal, lung, and ovarian carcinoma. As a classic cadherin, CDH6 will form homodimers and promote intercellular adhesion with itself and possibly, cadherin-9 and -14. Decreased expression of CDH6 may be associated with tumor growth and metastasis.

Specifications

Catalog NumberKC-3193
Cell Line NameCHOK1-CDH6-Cell-Line
Host Cell LineCHOK1
DescriptionStable CHOK1 cell line expressing exogenous human CDH6 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% RPMI1640+20% FBS+10% DMSO
Propagation MediumRPMI1640+10%FBS+10µg/mL Puromycin
Selection MarkerPuromycin
MorphologyFibroblastoid cells growing as a monolayer
SubcultureSplit saturated culture 1:4-1:8 every 2-3 days; seed out at about 1-2 × 105 cells/mL
Incubation37 °C with 5% CO2
StorageLiquid nitrogen immediately upon receiving
Doubling TimeApproximately 34 hours
Mycoplasma StatusNegative
In Vivo ValidationNA

Cell Line Generation

CHO-K1 human CDH6 cell line was generated using a lentiviral vector expressing the human CDH6 sequence.

Characterization

Figure: Characterization of human CDH6 overexpression in CHO-K1 stable clones using FACS.

Cell Resuscitation

  1. Prewarm culture medium ((RPMI1640 supplemented with 10% FBS and 10ug/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 1:4-1:8 every 2-3 days; seed out at about 1-2 × 105 cells/mL.

Cell Freezing

  1. Prepare the freezing medium (70% RPMI-1640 + 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. Shimoyama, Y. et al. (2000) Biochem. J. 349:159..
  2. Shimoyama, Y. et al. (1999) J. Biol. Chem. 274:11987.
  3. Shimoyama Y, Gotoh M, Terasaki T, Kitajima M, Hirohashi S (June 1995). Isolation and sequence analysis of
  4. human cadherin-6 complementary DNA for the full coding sequence and its expression in human carcinoma
  5. cells. Cancer Res. 55 (10): 2206–11. PMID 7743525.
  6. Chalmers IJ, Hofler H, Atkinson MJ (June 1999). Mapping of a cadherin gene cluster to a region of
  7. chromosome 5 subject to frequent allelic loss in carcinoma. Genomics. 57 (1): 160–3.
  8. doi:10.1006/geno.1998.5717. PMID 10191097.
  9. Entrez Gene: CDH6 cadherin 6, type 2, K-cadherin (fetal kidney).
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