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Transfection Reagent for HT-29 Cells (Colorectal Adenocarcinoma Cells)
- A nanoparticle-based liposome formulation
Transfection protocols provided for transfection of proteins, DNA, mRNA, siRNA, shRNA and microRNA
Transfection Enhancer reagent provided with the kit
Produce higher level of recombinant protein expression with minimal disruption of normal cell function
Generate physiologically relevant data you can trust
Effective for plasmid DNA/siRNA co-transfection
Easy-to-use transfection protocol with reproducible results
Download PowerPoint presentation for HT-29 cells transfection kit: [PPT]
Developed and manufactured by Altogen Biosystems
Reagent exhibits at least 70% transfection efficiency of siRNA delivery. Transfection efficiency was determined by qRT-PCR.
Transfection Protocol and MSDS:
Download Altogen Biosystems Transfection Protocol: [PDF]
Download MSDS: [PDF]
HT-29 Cell Line:
HT-29 was derived in 1964 from the tumor of a 44-year-old woman with colon adenocarcinoma in 1964. HT29 cells are human intestinal epithelial cells which produce the secretory component of Immunoglobulin A (IgA) and carcinoembryonic antigen (CEA). The HT-29 line is designated heterotransplantable, forming well-differentiated grade I tumors. The structure of HT-29 cells include microvilli, microfilaments, mitochondria, smooth and rough endoplasmic reticulum with free ribosomes, lipid droplets, limited primary lysosomes and many secondary lysosomes. The cells express urokinase receptors, but do not have detectable plasminogen activator activity. HT-29 cells have been shown to be negative for CD4, but there is expression of galactose ceramide. HT-29 cells are used for tumorigenicity studies. HT-29 cell line is extensively used as model system to study epithelial differentiation in vitro.
Figure 1. siRNAs targeting Lamin A/C mRNA or non-silencing control siRNA were transfected into HT-29 cells following the recommended protocol. At 48 hours post-transfection the cells were analyzed by qRT-PCR for Lamin A/C gene expression levels. 18S rRNA levels were used to normalize the Lamin A/C data. Values are normalized to untreated sample. Data are means ± SD (n=4).
Figure 2. Protein expression of Lamin A/C in HT-29 cells. DNA plasmid expressing Lamin A/C or siRNA targeting Lamin A/C were transfected into HT-29 cells following Altogen Biosystems transfection protocol. At 72 hours post-transfection the cells were analyzed by Western Blot for protein expression levels (normalized by total protein, 10 µg of total protein loaded per each well). Untreated cells used as a negative control.
Selected HT-29 transfection reagent citations:
- Clinical Cancer Research. 2010 16(16). Inhibition of Hypoxia Inducible Factor-1α by Dihydroxyphenylethanol … Terzuoli et al [PDF]
- Oncogene. 2012 (31). EGFR signaling upregulates expression of microsomal prostaglandin E … Donnini et al [PDF]
Altogen Biosystems provides preoptimized transfection products for life science research applications. Transfection protocols are optimized for individual cancer cell lines. Altogen Biosystems developed two types of in vivo delivery kits for animal research: Tissue-targeted reagents (delivery to liver, pancreas, and kidney tissues), and broad range in vivo delivery reagents (PEG-Liposome, Nanoparticle-based, Lipid-based, and Polymer-based kits). Advanced formulation of reagents and optimized transfection protocols provide efficient intracellular delivery of proteins, DNA, RNA, and any other negatively charged molecules in vitro and in vivo. Read more about transfection technology at Altogen’s Transfection Resource.
Altogen Labs Research Services:
Altogen Labs provides GLP-compliant contract research studies for pre-clinical research, IND applications, and drug development. Biology CRO services include: Xenograft models (30+), development of stable cell lines, ELISA assay development, cell-based and tissue targeted RNAi studies, safety pharm/tox assays, and other studies (visit AltogenLabs.com).
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