
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
TAL1 CRISPR/Cas9 KO Plasmid (h2) | sc-401101-KO-2 | 20 µg | $397.00 |
TAL1 (T-cell acute lymphocytic leukemia protein 1) is a basic helix–loop–helix transcription factor that regulates lineage specification and differentiation programs in hematopoietic development, particularly erythroid and T-cell compartments. It functions within multiprotein transcriptional complexes with partners such as E2A/TCF3, LMO2, LDB1, and GATA factors to control enhancer activity and chromatin accessibility at genes governing proliferation and maturation. TAL1 integrates signaling and transcriptional networks that shape hematopoietic stem/progenitor cell fate decisions and maintains context-dependent transcriptional states. Dysregulated TAL1 expression or enhancer hijacking is strongly associated with T-cell acute lymphoblastic leukemia biology and broader perturbations of hematopoietic transcriptional circuitry.
TAL1 CRISPR/Cas9 KO Plasmid (h2) is a pool of plasmids designed for targeted disruption of the TAL1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the TAL1 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 TAL1 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 TAL1 protein expression.
This CRISPR knockout system enables efficient generation of TAL1-deficient cell models for investigation of TAL1 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.