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UM-SCC-127
Tissue
Head and neck, oral cavity
Disease
Head and neck squamous cell carcinoma (HNSCC)

Documents

UM-SCC-127

Cell line · Product number 305725

UM-SCC-127 is a human HNSCC cell line from the University of Michigan UM-SCC panel. As part of the higher-numbered UM-SCC series, it represents one of the...

€800.00excl. tax and shipping

Customization / Recommendations

In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

UM-SCC-127 is a human HNSCC cell line from the University of Michigan UM-SCC panel. As part of the higher-numbered UM-SCC series, it represents one of the more recently established lines in this collection. The line grows adherently with epithelial-like morphology and provides a model for comparative molecular and pharmacological HNSCC studies.

Applicable in HNSCC research, drug sensitivity studies, molecular pathway analysis, and UM-SCC multi-line panel experiments. Suitable for pharmacological assays and xenograft models.

Tissue
Head and neck, oral cavity
Disease
Head and neck squamous cell carcinoma (HNSCC)
Applications
HNSCC research; drug sensitivity; molecular pathway analysis; UM-SCC panel studies; xenograft models

02Classification

Organism
Human
Sex
Unspecified
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
Epithelial-like
Cell type
Epithelial cells
Doubling time
approx. 24 to 48 hours

04Identifiers

Citation
UM-SCC-127 (Cytion catalog number 305725)
NCBI TaxID
9606

05Handling 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
Dissociation reagent
Accutase, 5 min., 37°C
Subculturing
Remove medium, wash with PBS without calcium and magnesium, cover with Accutase, incubate 8–10 min at RT, resuspend in medium, centrifuge 300×g 3 min, discard supernatant, reseed in fresh medium.
Split ratio
1 to 5
Seeding density
1 to 3 × 104 cells/cm2
Fluid renewal
Every 2 to 3 days
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 200 x g for 5 minutes, carefully discard the supernatant containing freezing medium.

  7. Follow the procedure described under Post-Thaw Recovery

06Quality control and cryopreservation

Freeze medium
As a cryopreservation medium, we use complete growth medium + 10% DMSO for adequate post-thaw viability.
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.

07Donor

Donor age
Age unspecified
Ethnicity
Ethnicity unspecified