
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Troponin T-C CRISPR/Cas9 KO Plasmid (h) | sc-400949 | 20 µg | $397.00 |
TNNT2 encodes cardiac troponin T, a core component of the troponin complex that couples Ca²⁺ signaling to thin-filament regulation of actin–myosin interaction in striated muscle. By anchoring the troponin complex to tropomyosin, TNNT2 helps coordinate sarcomere contraction dynamics, myofibrillar organization, and excitation–contraction coupling within cardiomyocytes. Genetic variation or dysregulated expression of TNNT2 is linked to inherited cardiomyopathies and contractile dysfunction, making it a key molecular entry point for studying sarcomeric biology, calcium-handling networks, and stress-response pathways in human cardiac cells. TNNT2 is therefore widely used as a functional node for modeling disease-associated remodeling, assessing myofilament sensitivity, and benchmarking cardiomyocyte maturation in vitro.
Troponin T-C CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the TNNT2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the TNNT2 together with the Streptococcus pyogenes Cas9 nuclease. The plasmids also encode GFP, allowing fluorescent identification and enrichment of successfully transfected cells by fluorescence microscopy or flow cytometry.
The multi-guide design increases the likelihood of generating insertions or deletions (indels) that disrupt the TNNT2 open reading frame following Cas9-mediated double-strand break formation. DNA breaks introduced by the CRISPR/Cas9 system are repaired through endogenous non-homologous end joining (NHEJ) pathways, frequently resulting in frameshift mutations that abolish Troponin T-C protein expression.
This CRISPR knockout system enables efficient generation of TNNT2-deficient cell models for investigation of Troponin T-C signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.