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NCI-H1651

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Cat. No.: CL-1178
NCI-H1651 - 1
  • NCI-H1651NCI-H1651 - 1
  • NCI-H1651NCI-H1651 - 2
  • NCI-H1651NCI-H1651 - 3
  • +2

CL-1178

$ 600.00

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1×10^6Cells/Vial×2Vials

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Product Introduction

General information
Cell Name NCI-H1651
Synonyms H1651;H-1651;NCIH1651
Cellosaurus Accession CVCL_1484
Organism Human
Growth Properties Adherent
Morphology Epithelial-like
Tissue Lung
Age 71Y
Sex Male
Instructions 1. Check all containers for leakage or breakage.
2. Remove the frozen cells from the dry ice packaging and immediately transfer them to liquid nitrogen (liquid or vapor phase) for long-term cryopreservation.
3. Fewer floating cells and a small number of vacuoles are present during cell culture.
4. When cells are cultured in conventional DM/F12 + 10% FBS, extensive vacuolization occurs and cells do not proliferate. Be sure to use complete medium for culture.
Complete Medium DMEM/F12, with HEPES [PM150310]+0.5% ITS-G [PB180429]+1 ng/mL EGF+50 nM Supplement1+0.01 mM Supplement2+0.01 mM Supplement3+0.5 mM sodium pyruvate [PB180422]+2 mM L-Glutamine [PB180420]+100 pM Supplement4+10% Nutrient+1% Supplement5
Incubation Atmosphere Air, 95%; CO₂, 5%
Temperature 37℃
Subcultivation Ratio 1:2-1:3
Medium Renewal 2 to 3 times per week
Dissociation Duration 3-4 min
Subculturing Procedure 1. Remove the culture medium from the T25 cell culture flask.
2. Add approximately 2 mL of PBS. Gently tilt the flask side to side until the PBS covers the entire bottom, then aspirate and discard the PBS.
3. Add 1 mL of 0.25% trypsin solution (containing EDTA). Gently tilt the flask side to side until the trypsin solution covers the entire bottom of the flask.
4. Incubate the cells at 37°C. Observe the cells under an inverted microscope and terminate digestion once the cells round up and detach. To avoid clumping, do not agitate the cells by tapping or shaking the flask during detachment.
5. Add 3 mL of complete culture medium to terminate digestion and disperse into a single cell suspension.
6. Collect the cell suspension and centrifuge at 1200 rpm (approximately 250 ×g) for 3 minutes. Carefully aspirate and discard the supernatant.
7. Add fresh complete culture medium, pipette gently several times to resuspend the cells, and seed them at the appropriate ratio into a new culture flask. Loosen the cap or use a vented cap for incubation.
Freeze Medium General Freezing Medium [PB180436]
Storage Conditions For long-term cryopreservation, cryovials should be stored in liquid nitrogen at −150°C to −196°C. Storage at −80°C is restricted to short-term interim use only.
Background NCI-H1651 is a cell line isolated from the lungs of a 71-year-old male patient with non-small cell lung cancer: adenocarcinoma.
Biosafety Level BSL-1

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