9L/lacZ cell

SKU:BHC11101188
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Overview
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9L/lacZ cell is a cell line (Male). It is commonly used as an in vitro model for 1 research. Growth characteristics: Adherent, Fibroblast. Supplied as cryopreserved cells with accompanying batch CoA and quality-control documentation.

Species Rat
Disease model Rat malignant glioma
Morphology Fibroblast
Growth Properties Adherent
Tissue Brain
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Catalog no. Size
305208 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 305208
Species Rat
The 9L/lacZ cell line is a well-characterized rat gliosarcoma cell line commonly used in neurobiological and oncological research. Originally derived from a nitrosourea-induced rat brain tumor, this line has been engineered to express the lacZ gene, which encodes the enzyme β-galactosidase. This modification facilitates the tracing and studying of tumor cells in vivo, particularly useful in experiments involving tumor progression and metastasis. The expression of lacZ allows for the easy identification of these cells using X-gal staining, which turns the cells blue when they express β-galactosidase. These cells exhibit aggressive tumor-forming capabilities when implanted in immunocompromised or syngeneic hosts, making them a robust model for studying brain cancer dynamics and testing therapeutic strategies against gliomas. Additionally, the 9L/lacZ cell line has been utilized in gene therapy trials, particularly in assessing the efficacy of suicide genes and other genetic interventions aimed at controlling tumor growth. This line is also pivotal in understanding the interactions between tumor cells and the host's immune system, thereby contributing insights into the complexities of tumor immunology.

SKU:BHC11101188

  • cultureMedium: DMEM, w: 4.5 g/L Glucose, w: 4 mM L-Glutamine, w: 3.7 g/L NaHCO3, w: 1.0 mM Sodium pyruvate (Cytion article number 820300a)
  • supplements: Supplement the medium with 10% FBS
  • 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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