B16F10 Cells
Products
B16F10-Fluc-Neo/mNIS-Puro $ 2,100
B16F10-mNIS (monoclonal) $ 2,500
B16F10-mNIS-Neo/eGFP-Puro $ 2,100
B16F10-mNIS-Neo/iRFP-Puro $ 2,100
B16F10-mNIS-Puro $ 1,500
Description:
Usage Information:
B16F10 cells are suitable for in vitro and in vivo experimentation. Both syngenic C57BL/6 mice and immunocompromised mice can be used for in life studies, and will form tumors following implantation of the cells.
The following chart provides some examples of B16F10 cells used for tumor formation and studies.
Route of Implantation |
Mice |
Tumor/Metastases |
References |
---|---|---|---|
Subcutaneous |
C57BL/6 |
Subcutaneous tumor |
Zhang et al. (2015) BMC Cancer 15: 234. Takeda et al. (2015) Blood 118: 464-472. |
Tail vein |
C57BL/6 |
Lung metastases |
Zhang et al. (2015) BMC Cancer 15: 234. Takeda et al. (2015) Blood 118: 464-472. Fidler (1975) Cancer Res 35: 218-224. Burghoff et al. (2014) BMC Cancer 14: 898. |
Subcutaneous |
C57BL/6 |
Subcutaneous tumor, lung metastases |
Fidler (1975) Cancer Res 35: 218-224. |
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 B16F10 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 B16F10 cells are available with a variety of different reporters, including the murine sodium iodide symporter (mNIS), firefly luciferase (Fluc), enhanced green fluorescent protein (eGFP), or near-infrared fluorescent protein (iRFP). Several dual reporter B16F10 cell lines are available to facilitate multi-modality imaging.
In order to ensure high, constitutive expression of the reporter proteins, our cell lines are generated by lentivirus transduction. The lentivirus 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 lentiviruses by preventing mobilization of replication competent viruses (Miyoshi et al., J Virol. 1998).
For more information about a specific reporter and its uses, click on the photos below.