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NCI-H69 (H69)
Tissue
Lung
Disease
Lung small cell carcinoma
Metastatic site
Pleural effusion
Synonyms
NCI-H-69, NCI H69, H69, H-69, NCIH69, NCI-HUT-69, H69/P, NCI-H69C, H69C, H69c

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NCI-H69 (H69)

Cell line · Product number 300185

This cell line is aneuploid, will form colonies in soft agar and retains small cell carcinoma morphology and ultrastructure as well as APUD cell characterist...

€430.00excl. tax and shipping

Customization / Recommendations

In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description
This cell line is aneuploid, will form colonies in soft agar and retains small cell carcinoma morphology and ultrastructure as well as APUD cell characteristics. The cells grow in aggregates, thus cell counts are not accurate. The line can be adapted to grow in shaker flask or spinner flask systems. These cells are not resistant to Adriamycin.
Tissue
Lung
Disease
Lung small cell carcinoma
Metastatic site
Pleural effusion
Synonyms
  • NCI-H-69
  • NCI H69
  • H69
  • H-69
  • NCIH69
  • NCI-HUT-69
  • H69/P
  • NCI-H69C
  • H69C
  • H69c

02Classification

Organism
Human
Sex
Male
Biosafety level
1

03Characteristics

Tumourigenic
Forms tumors with typical small cell carcinoma histology
Karyotype
Aneuploid, with 3p deletion. Range = 40 to 73
Doubling time
69 hours

04Identifiers

Citation
NCI-H69 (H69) (Cytion catalog number 300185)
NCBI TaxID
9606
Cellosaurus
CVCL_1579

05Expression and susceptibility

Receptors expressed
Insulin-like growth factor II receptor (IGF II)
Protein expression
P53 negative, cytokeratins positive
Isoenzymes
G6PD, B, PGM1, 2, PGM3, 1, ES-D, 2, Me-2, 1, AK-1, 1, GLO-1, 1-2, Phenotype Frequency Product: 0.00006

06Handling and culture

Culture medium
RPMI 1640, w: 2.0 mM stable Glutamine, w: 2.0 g/L NaHCO3 (Cytion article number 820700a)
Incubation atmosphere

37°C, 5% CO2, humidified atmosphere.

Supplements
Supplement the medium with 10% FBS
Subculturing
Allow aggregates to settle to the bottom of the flask, remove and discard the supernatant medium. Add fresh medium, disperse cells by gentle pipetting and dispense into new flasks. Subculture every 6 to 8 days.
Seeding density
1 x 105 cells/ml
Fluid renewal
2 to 3 times per week
Post-thaw recovery
After thawing allow the cells to recover from the freezing process for at least 24 hours.
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

07Quality control and cryopreservation

Sterility

Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods.

To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections.

Freeze medium
As a cryopreservation medium, we use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress.
Storage conditions

For long-term preservation, place vials in vapor-phase liquid nitrogen at about −150 to −196 °C. Storage at −80 °C is acceptable only as a short interim step before transfer to liquid nitrogen.

Shipping conditions

Cryopreserved cell lines are shipped on dry ice in validated, insulated packaging with sufficient refrigerant to maintain approximately −78 °C throughout transit. On receipt, inspect the container immediately and transfer vials without delay to appropriate storage.

08Donor

Donor age
55 years
Ethnicity
Caucasian