KC-0961

NCI-H1155-CRBN-KO-2B1-Cell-Line

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Background of NCI-H1155-CRBN-KO-2B1-Cell-Line

The CRBN gene, encoding cereblon, is a ubiquitously expressed protein that plays a critical role in the ubiquitin-proteasome system. Cereblon functions as an E3 ubiquitin ligase substrate receptor, participating in the degradation of specific target proteins. Notably, cereblon is best known for its involvement in the mechanism of action of thalidomide and its analogs, which are used therapeutically in the treatment of multiple myeloma and other hematological malignancies. These drugs enhance the binding affinity of cereblon for neomorphic substrates, leading to their ubiquitination and subsequent degradation.

Specifications

Catalog NumberKC-0961
Cell Line NameNCI-H1155-CRBN-KO-2B1-Cell-Line
Host Cell LineNCI-H1155
DescriptionStable NCI-H1155 clone with human CRBN gene knockout, No.2B1
QuantityTwo vials of frozen cells (≥2-106/vial)
StabilityStable in culture over a minimum of 10 passages
ApplicationDrug screening and biological assays
Freezing MediumRPMI1640+20% FBS+10% DMSO
Propagation MediumRPMI1640+10% FBS
Selection MarkerN/A
MorphologyEpithelial
SubcultureSplit saturated culture 1:3-1:6 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

NCI-H1155-CRBN-KO-2B1 cell line was generated using the CRISPR method.

Characterization

Figure 1: Characterization of NCI-H1155-CRBN-KO-2B1 cell line stable clone using PCR sequencing.

Figure 2: Characterization of NCI-H1155-CRBN-KO-2B1 cell line stable clone using western blot.

Cell Resuscitation

  1. Prewarm culture medium (RPMI1640 + 10% FBS)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 1:3-1:6 every 2-3 days; seed out at about 1-3 × 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. Kubacka, J., et al. (2015). Cereblon is a thalidomide analogue-binding receptor and mediates thalidomide-induced teratogenicity.Nature, 520(7546), 327-331. https://doi.org/10.1038/nature14197
  2. Mikaelian, I., et al. (2017). Cereblon: from a mysterious teratogen target to a validated therapeutic target.Pharmacology & Therapeutics, 173, 1-12. https://doi.org/10.1016/j.pharmthera.2016.12.005
  3. Chen, X., et al. (2018). Structural basis for thalidomide-induced degradation of the transcription factor Ikaros.Science, 361(6401), 566-570. https://doi.org/10.1126/science.aar3202
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