C1498 (Leukemia)

C1498 (ATCC® TIB-49™) is a murine myeloid leukemia cell line isolated from a C57BL/6J mouse.  It most closely resembles acute myeloid leukemia (AML), and is highly lethal when implanted into syngeneic mice.

*The ATCC trademark and trade name and any and all ATCC catalog numbers are trademarks of the American Type Culture Collection.

Usage Information and Tips

C1498 cells are suitable for in vitro and in vivo experimentation. The cells will form tumors and spontaneous metastases in immunocompromised and syngeneic C57BL/6 mice. Depending on the route of inoculation (see below), implanted C1498 cells can metastasize to numerous sites including the bone marrow, liver, spleen, lymph nodes, kidney, skin, and central nervous system. The following chart provides some examples of C1498 cells used for tumor formation and studies.
Route of ImplantationMiceTumor/MetastasesReferences
IntravenousC57BL/6Bone marrow, liver, lymph nodes, ovary, subcutaneous masses, spleen, skin, kidney, and central nervous systemBoyer, et al. (1995) Blood 85: 2498-2506Zhang, et al. (2009) Blood 114: 1545-1552Sauer et al. (2004) Cancer Res 64: 3914-3921
SubcutaneousC57BL/6Subcutaneous tumorBoyer et al. (1997) Blood 89: 3477-3485
Note: The above information is based on available data from the indicated references. It is not meant to be comprehensive and Imanis has not directly tested each condition.

Stable Reporter Cell Lines

Our C1498 reporter cell lines can be tracked in vivo, making them great tools for studying the mechanisms of tumor growth and metastasis, as well as evaluating the effects of various drugs or therapies in animals. Our C1498 cells are available with firefly luciferase (Fluc) or enhanced green fluorescent protein (eGFP). Dual reporter cell lines are available to facilitate multimodal imaging.

In order to ensure high, constitutive expression of the reporter proteins, our cell lines are generated by lentiviral vector transduction. The lentiviral vectors used for these transductions are self-inactivating (SIN) vectors in which the viral enhancer and promoter has been deleted. This increases the biosafety of the lentiviral vectors by preventing mobilization of replication competent viruses (Miyoshi et al., J Virol. 1998).

Cell & Virus Products Built for Breakthroughs

Don’t see what you need in our catalog? Our scientific team engineers cell lines, viral vectors, and assays and provides as much characterization data as you need to move forward with confidence.