SCaBER cell

SKU:BHC11101036
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Overview
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SCaBER cell is a cell line derived from African (Male). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Epithelial. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Human
Disease model Bladder squamous cell carcinoma
Morphology Epithelial
Growth Properties Adherent
Tissue Urinary bladder
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Catalog no. Size
305111 1 cryovial
Available Options

This cell line is available in the U.S. For non-profit users, please sign and submit the Non-Profit Supply Agreement to orders@biohippo.com before placing an order. For commercial users, please complete the CLEAR Form before ordering, as additional usage fees may apply based on the intended use. For further details, please contact orders@biohippo.com. Products ship after the required agreement is completed; typical delivery is 2–3 business days. Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 10^6 cells for adherent lines or 5 × 10^6 cells for suspension lines (refer to the batch CoA for details).

Field Specification
Mfr No 305111
Species Human
The SCaBER cell line is derived from a human squamous cell carcinoma of the urinary bladder. Originating from a 58-year-old male patient, this cell line retains many of the original tumor’s features, including its squamous differentiation. SCaBER cells display a distinct epithelial morphology with prominent intercellular connections such as desmosomes and interdigitated microvilli. These characteristics make it an excellent model for studying the pathology and progression of squamous cell carcinoma in the bladder. SCaBER cells exhibit a hypotetraploid karyotype with a highly variable chromosomal number and the presence of distinctive marker chromosomes. The male karyotype includes both X and Y chromosomes, further distinguishing it from other cell lines. Ultrastructural studies reveal abundant tonofilaments, lipid bodies, and well-developed organelles such as the Golgi apparatus and rough endoplasmic reticulum. These properties have been maintained across multiple passages, ensuring consistency for long-term studies. This cell line has been utilized in immunological research to explore tumor-specific antigens and their role in bladder cancer progression. SCaBER's squamous differentiation is a key factor for investigations into tumor-associated antigens in squamous cell carcinomas, offering insights into potential diagnostic markers and therapeutic targets. Its well-characterized molecular and phenotypic properties make it a critical resource in urological cancer research.

SKU:BHC11101036

  • cultureMedium: EMEM (MEM Eagle), w: 2 mM L-Glutamine, w: 2.2 g/L NaHCO3, w: EBSS (Cytion article number 820100a)
  • supplements: Supplement the medium with 10% FBS and 1% NEAA
  • dissociationReagent: Accutase
  • subculturing: Remove the old medium from the adherent cells and wash them with PBS that lacks calcium and magnesium. For T25 flasks, use 3-5 ml of PBS, and for T75 flasks, use 5-10 ml. Then, cover the cells completely with Accutase, using 1-2 ml for T25 flasks and 2.5 ml for T75 flasks. Let the cells incubate at room temperature for 8-10 minutes to detach them. After incubation, gently mix the cells with 10 ml of medium to resuspend them, then centrifuge at 300xg for 3 minutes. Discard the supernatant, resuspend the cells in fresh medium, and transfer them into new flasks that already contain fresh medium.
  • fluidRenewal: 2 to 3 times per week
  • freezeMedium: As a cryopreservation medium, 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.
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