KC-6289

Eol-1-CCR6-KO cell line

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Home » Eol-1-CCR6-KO cell line

Background of Eol-1-CCR6-KO cell line

The CC chemokine receptor 6 (CCR6), alternatively known as STRL22, resides on chromosome 6q27 and functions as a homologous receptor for CCL20. It is also characterized as a 7-transmembrane domain G-protein coupled receptor, primarily expressed in leukocytes, and binds to CCL20 to mediate leukocyte migration. In tissues, it is predominantly expressed in the lymph nodes, appendix, and spleen, while showing lower levels of expression in the thymus, testis, and small intestine .

Specifications

Catalog NumberKC-6289
Cell Line NameEol-1-CCR6-KO cell line
Clone Number1A2
Host Cell LineEOL1
DescriptionStable Eol-1-CCR6-KO cell clone with human CCR6 gene knockout
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
MorphologyLymphoblast
SubcultureSplit the saturated culture at a ratio of 1:3-1:4 every 3-4 days; seed out at about 1-3 x 105 cells/mL
Incubation37 °C with 5% CO2
StorageLiquid nitrogen immediately upon receiving
Doubling TimeApproximately 32 hours
Mycoplasma StatusNegative

Cell Line Generation

Eol-1-CCR6-KO cell line was generated using the CRISPR method.

Characterization

Figure 1: Characterization of Eol-1-CCR6-KO cell line stable clone using PCR sequencing.

Figure 2:Characterization of Eol-1-CCR6-KO cell line stable clone using RT-PCR sequencing.

Figure 3:Characterization of Eol-1-CCR6-KO cell line stable clone using FACS.

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 1:3-1:4 every 3-4 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. Li Y-, Geng WL, Li CC, Wu JH, Gao F, Wang Y. Progress of CCL20-CCR6 in the airways: a promising new therapeutic target. J Inflamm (Lond). 2024 Dec 27;21(1):54. doi: 10.1186/s12950-024-00427-5. Erratum in: J Inflamm (Lond). 2025 Jan 13;22(1):2. doi: 10.1186/s12950-025-00428-y. PMID: 39731176; PMCID: PMC11681768.
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