CT26.WT-iRFP-Neo is a polyclonal population of the mouse colorectal carcinoma cell line CT26.WT (ATCC® CRL-2638™). To achieve stable reporter expression in the polyclonal population, parental CT26.WT cells were transduced with LV-iRFP-P2A-Neo (LV033) and selected using G418. LV-iRFP-P2A-Neo encodes the near-infrared fluorescent protein (iRFP) cDNA linked to the neomycin resistance gene (Neo) via a P2A cleavage site (P2A) under the spleen focus-forming virus (SFFV) promoter.

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This cell line has been tested for mycoplasma contamination and is certified mycoplasma free.

The parental CT26.WT cell line has been authenticated and certified free of interspecies cross contamination by short tandem repeat (STR) profiling with 9 STR loci.

Due to the immunogenicity of the reporter genes in this cell line, we recommend using immunocompromised mice for in vivo studies.

Replication Competent Lentivirus (RCL) Test (including a test report) is available for this cell line at an added cost.  Contact us to learn more.

In vivo Imaging

A Balb/c mouse was implanted with 5 x 10⁵ CT26.WT-iRFP-Neo (CL091) cells in the right hind flank. Tumor growth was monitored over time using calipers. Fluorescence imaging was performed on Day 30 using an IVIS Spectrum.

Morphology

Low and high density cell morphology (200x)

iRFP Expression

 CT26.WT-iRFP-Neo cells (red) or control (CT26.WT-Fluc-Neo; grey) cells were fixed with paraformaldehyde and analyzed by flow cytometry (20,000 events).

Complete Growth Medium: DMEM supplemented with 10% FBS, 1X Penicillin/Streptomycin, and 0.4 mg/mL G418.

The addition of G418 to the complete growth medium maintains high reporter expression over continued passage of the cells. It is highly recommended, especially if the cells undergo multiple passages prior to being used for studies.

These cells should be grown in the indicated medium and passaged when they reach confluency. For routine passaging, cells are recommended to be split at a 1:10 ratio every 3-4 days.

CT26.WT cells easily detach from tissue culture surfaces. Coating culture plates with poly-D-Lysine prior to use is recommended for applications involving frequent washes, culture media changes, or rocking.

These cells are suitable for in vitro and in vivo experimentation. CT26.WT cells form tumors and pulmonary metastases post implantation into syngenic Balb/c mice.¹ The iRFP transgene facilitates in vivo and ex vivo fluorescence imaging of implanted cells. To reduce background autofluorescence, mice should be fed an alfalfa-free diet for at least a week prior to imaging.

The cells can be amplified in vitro and used to generate additional frozen stocks. Cryopreservation of low passage stocks is recommended. Frozen stocks should be preserved in a designated cryopreservation medium.

These cells were generated via lentiviral vector transduction. The lentiviral vector used for transduction was a self-inactivating (SIN) vector in which the viral enhancer and promoter have been deleted. Transcription inactivation of the LTR in the SIN provirus increases biosafety by preventing mobilization by replication competent viruses and enables regulated expression of the genes from the internal promoters without cis-acting effects of the LTR². Nevertheless, all work with these cells should be performed under biosafety-level 2 (BSL2) conditions by trained personnel. Institutional requirements may permit handling of these cells under BSL1 conditions if certain criteria are met.

References:
¹Wang et al. J Immunol. 1995. 154:4685-4692.
³Miyoshi et al. J Virol 1998. 72:8150-8157.