kc-4874

LNcap-STEAP3-KO Cell Line

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Home » LNcap-STEAP3-KO Cell Line

Background of LNcap-STEAP3-KO Cell Line

This gene encodes a multipass membrane protein that functions as an iron transporter. The encoded protein can reduce both iron (Fe3+) and copper (Cu2+) cations. STEAP3 contains a functional p53-binding site in its promoter and can be upregulated following p53 activation to enhance cell death in myeloid leukemia cell line and breast cancer cells. Deficiency in this gene can cause anemia. Alternative splicing results in multiple transcript variants.

Specifications

Catalog Numberkc-4874
Cell Line NameLNcap-STEAP3-KO Cell Line
Clone Number1A3
Host Cell LineLNcap
DescriptionStable LNcap clone with human STEAP3 gene knockout, No.1A3
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 Medium90% RPMI1640+10% FBS
Selection MarkerNA
Morphologyepithelial
SubcultureSplit saturated culture 1:4-1:6 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 60 hours
Mycoplasma StatusNegative

Cell Line Generation

LNcap-STEAP3-KO cell line was generated using the CRISPR method.

Characterization

Figure 1: Characterization of LNcap-STEAP3-KO cell line stable clone using PCR sequencing.

Figure 2: Characterization of LNcap-STEAP3-KO cell line stable clone using RT-PCR sequencing.

Cell Resuscitation

  1. Prewarm culture medium (90% 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 1:4-1:6 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. Wang LL, Luo J, He ZH, Liu YQ, Li HG, Xie D, Cai MY. STEAP3 promotes cancer cell proliferation by facilitating nuclear trafficking of EGFR to enhance RAC1-ERK-STAT3 signaling in hepatocellular carcinoma. Cell Death Dis. 2021 Nov 5;12(11):1052. doi: 10.1038/s41419-021-04329-9. PMID: 34741044; PMCID: PMC8571373.
  2. https://www.ncbi.nlm.nih.gov/gene/55240
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