KC-1986

HEK293T-NKG2A-Cell-Line

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Home » 细胞系 » HEK293T-NKG2A-Cell-Line

Background of HEK293T-NKG2A-Cell-Line

NKG2, also named as KLRC1 or CD159a, is a type II transmembrane protein predominately expressed in NK cells. NKG2 has two isoforms, NKG2A and NKG2B, both of which contain immunoreceptor tyrosine-based inhibition motifs (ITIMs) in the intracellular part of the molecule, NKG2A can form heterodimers with CD94, linked by disulfide bonds and play an inhibitory role in immunological process after recognizes non-classical major histocompatibility (MHC) class Ib molecule HLA-E loaded with self-peptides derived from the signal sequence of classical MHC class Ia molecules.

Specifications

Catalog NumberKC-1986
Cell Line NameHEK293T-NKG2A-Cell-Line
Host Cell LineHuman HEK293T cell line
DescriptionStable HEK293T cell line expressing exogenous human NKG2A 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% DMEM+20% FBS+10% DMSO
Propagation MediumDMEM+10%FBS+1µg/mL Puromycin
Selection MarkerPuromycin
MorphologyEpithelial
SubcultureSplit saturated culture 1:3-1:6 every 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

293T human NKG2A cell line was generated using a lentiviral vector expressing the human NKG2A sequence.

Characterization

Cell Resuscitation

  1. Prewarm culture medium (DMEM + 10% FBS + 1µg/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 1:3-1:6 every 3 days; seed out at about 1-3 × 105 cells/mL.

Cell Freezing

  1. Prepare the freezing medium (70% DMEM + 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. Borrego, F., Masilamani, M., Marusina, A. I., Tang, X. & Coligan, J. E. The CD94/NKG2 family of receptors: from molecules and cells to clinical relevance. Immunol Res 35, 263ÿ278 (2006).
  2. Gunturi, A., Berg, R. E. & Forman, J. The role of CD94/NKG2 in innate and adaptive immunity. Immunol Res 30, 29ÿ34 (2004).
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