KC-4464

CHOK1-cyno-PTH1R-Cell-Line

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Home » CHOK1-cyno-PTH1R-Cell-Line

Background of CHOK1-cyno-PTH1R-Cell-Line

PTH1R, also known as PTHR1, is a protein that belongs to the G-protein coupled receptor 2 family. PTH1R is a receptor for parathyroid hormone and for parathyroid hormone-related peptide. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase, and phosphatidylinositol-calcium second messenger system. Diseases associated with PTH1R include Jansen type metaphyseal chondrodysplasia and Blomstrand type Chondrodysplasia. Among its related pathways are endochondral ossification with skeletal dysplasias and GPCR downstream signaling.

Specifications

Catalog NumberKC-4464
Cell Line NameCHOK1-cyno-PTH1R-Cell-Line
Host Cell LineCHOK1
DescriptionStable CHOK1 clone expressing exogenous cyno-PTH1R 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% RPMI 1640 + 20% FBS + 10% DMSO
Propagation MediumRPMI 1640 + 10% FBS + 10μg/mL Puromycin
Selection MarkerPuromycin
MorphologyEpithelial
SubcultureSplit saturated culture 1:6-1:8 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 24 hours
Mycoplasma StatusNegative
In Vivo ValidationNA

Cell Line Generation

CHOK1-cyno-PTH1R-cell-line was generated using a lentiviral vector expressing the cyno-PTH1R sequence.

Characterization

Figure 1: Characterization of cyno-PTH1R overexpression in the CHOK1-cyno-PTH1R stable clone using qPCR.

Figure 2: Characterization of cyno-PTH1R in the CHOK1-cyno-PTH1R stable clone using PCR sequencing.

Cell Resuscitation

  1. Prewarm culture medium (RPMI 1640 supplemented with 10% FBS and 10μg/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 1:6-1:8 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. Structure of the parathyroid hormone receptor C terminus bound to the G-protein dimer Gbeta1gamma2. PMID: 18611381 PMCID: PMC2601695 DOI: 10.1016/j.str.2008.04.010.
  2. Dimeric arrangement of the parathyroid hormone receptor and a structural mechanism for ligand-induced dissociation. PMID: 20172855 PMCID: PMC2852981 DOI: 10.1074/jbc.M109.093138.
  3. Entrez Gene: PTH1R parathyroid hormone 1 receptor.
  4. Yamaguchi T, Hosomichi K, Narita A, Shirota T, Tomoyasu Y, Maki K, Inoue I (Jul 2011). Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese. Journal of Bone and Mineral Research. 26 (7): 1655ÿ61. doi:10.1002/jbmr.385. PMID 21404329. S2CID 23855913.
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