LM/TK(LMTK-) Cells
CAD$545.10*
Products are shipped frozen on dry ice in cryotubes. Each cryotube typically contains 3 × 106 cells for adherent lines or 5 × 106 cells for suspension lines (refer to the batch CoA for details).
General information
| Description | The LM/TK- (LMTK-) cell line is derived from murine fibroblasts and is characterized by the lack of thymidine kinase (TK) activity. This cell line is particularly useful in genetic and molecular biology research, where it serves as a model system for studying gene function, DNA replication, and recombination. The absence of TK in these cells allows for the selection of mutants or recombinant cells that have regained TK activity, making them valuable in studies involving TK-deficient mutants and for the selection of TK-positive clones following transfection with exogenous DNA. This cell line, derived from a sub-line of the L-M mouse fibroblast cell line which is resistant to BUdR, is potentially used for genetic and biochemical studies such as gene transfer and somatic cell hybridization. LM/TK- cells are commonly employed in research involving the herpes simplex virus (HSV) thymidine kinase gene, as they provide a crucial background for the selection of HSV-TK gene transformants. This has significant implications in gene therapy research, where HSV-TK is used in suicide gene therapy strategies to selectively kill cancer cells. Furthermore, these cells are utilized in the production of recombinant viruses and in the analysis of viral gene expression and replication. The LMTK- cell line thus plays a critical role in advancing our understanding of genetic manipulation and the development of therapeutic strategies. |
|---|---|
| Organism | Mouse |
| Tissue | Subcutaneous Connective Tissue, Mammary Areola And Fat |
| Synonyms | L-M[TK-], LM TK negative, L-M (TK-), L M (TK-), LM(TK-), LM(tk-), LM-TK-, LMTK-, L cells (TK-), L(TK-), L(tk-) |
Characteristics
| Breed/Subspecies | C3H/An |
|---|---|
| Age | 100 days |
| Gender | Male |
| Morphology | Fibroblast-Like |
| Growth properties | Adherent |
Regulatory Data
| Citation | LM/TK(LMTK-) (Cytion catalog number 305176) |
|---|---|
| Biosafety level | 1 |
| NCBI_TaxID | 10090 |
| CellosaurusAccession | CVCL_4536 |
Biomolecular Data
| Antigen expression | H-2k |
|---|---|
| Tumorigenic | Yes, in nude mice (Tumors developed within 21 days at 100% frequency (5/5) in nude mice inoculated subcutaneously with 1×107 cells). |
Handling
| Culture Medium | 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 |
| Dissociation Reagent | 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. |
| Fluid renewal | 2 times per week |
| 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. |
| Thawing and Culturing Cells |
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| Incubation Atmosphere | 37°C, 5% CO2, humidified atmosphere. |
| 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. |
| 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. |
Quality Control & Molecular Analysis
| 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. |
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Certificate of Analysis (CoA)
| Lot Number | Certificate Type | Date | Catalog Number |
|---|---|---|---|
| 305176-100725 | Certificate of Analysis | 18. Aug. 2025 | 305176 |