KC-3051-DW

CT26-mDDR1-KO-3B1 Cell Line

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Home » 细胞系 » CT26-mDDR1-KO-3B1 Cell Line

Background of CT26-mDDR1-KO-3B1 Cell Line

Discoidin Domain Receptor 1 (DDR1) is a protein that belongs to the discoidin domain receptor family. It is a transmembrane receptor tyrosine kinase that plays an important role in cell adhesion, migration, and proliferation. DDR1 is expressed in various tissues, including the heart, kidney, lung, liver, and brain, and has been implicated in several physiological and pathological processes. For example, DDR1 is involved in the regulation of collagen synthesis and deposition, which is important for tissue remodeling during wound healing and fibrosis. It is also involved in the regulation of cell survival and apoptosis, as well as in the development and progression of cancer. Mutations or dysregulation of DDR1 have been associated with several diseases, including cancer, fibrosis, and cardiovascular disease. As a result, DDR1 has become a potential therapeutic target for the treatment of these diseases.

Specifications

Catalog NumberKC-3051-DW
Cell Line NameCT26-mDDR1-KO-3B1 Cell Line
Host Cell LineCT26
DescriptionStable CT26 clone with mDDR1 gene knockout, No.3B1
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
Selection MarkerNA
MorphologyFibroblast
SubcultureSplit saturated culture 1:4-1:5 every 1-2 days; seed out at about 1 × 105 cells/mL
Incubation37 °C with 5% CO2
StorageLiquid nitrogen immediately upon receiving
Doubling TimeApproximately 24 hours
Mycoplasma StatusNegative
In Vivo ValidationYes

Cell Line Generation

CT26-mDDR1-KO cell line was generated using CRISPR method.

Characterization

Figure 1: Characterization of CT26-mDDR1-KO-3B1 cell line stable clone using PCR sequencing.

Figure 2: Characterization of CT26-mDDR1-KO-3B1 cell line stable clone using RT-PCR sequencing.

Figure 3: Characterization of CT26-mDDR1-KO-3B1 Cell Line stable clone using western blot.

Figure 4: Morphology of CT26-mDDR1-KO-3B1 Cell Line.

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 1:4-1:5 every 2-3 days; seed out at about 1-3 × 105 cells/mL.

Cell Freezing

  1. Prepare the freezing medium (70% RPMI1640 + 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. Guo J, Zhang Z, Ding K. A patent review of discoidin domain receptor 1 (DDR1) modulators (2014-present). Expert Opin Ther Pat. 2020 May;30(5):341-350. doi: 10.1080/13543776.2020.1732925. Epub 2020 Feb 26. PMID: 32077340.
  2. Moll S, Desmoulière A, Moeller MJ, Pache JC, Badi L, Arcadu F, Richter H, Satz A, Uhles S, Cavalli A, Drawnel F, Scapozza L, Prunotto M. DDR1 role in fibrosis and its pharmacological targeting. Biochim Biophys Acta Mol Cell Res. 2019 Nov;1866(11):118474. doi: 10.1016/j.bbamcr.2019.04.004. Epub 2019 Apr 5. PMID: 30954571.
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