
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Aldehyde dehydrogenase 3-A2/ALDH3A2 CRISPR/Cas9 KO Plasmid (h) | sc-405313 | 20 µg | $397.00 |
Human ALDH3A2 (fatty aldehyde dehydrogenase, FALDH) is an NAD-dependent enzyme that oxidizes medium- and long-chain aliphatic aldehydes to their corresponding fatty acids, limiting the accumulation of reactive lipid aldehydes generated during lipid metabolism and oxidative stress. It is a key component of fatty alcohol and sphingolipid catabolism, including the degradation of fatty aldehydes derived from plasmalogen and ether lipid turnover. By controlling aldehyde burden, ALDH3A2 contributes to membrane lipid homeostasis and cellular redox balance. Loss-of-function variants are associated with Sjögren–Larsson syndrome and are studied in the context of neurocutaneous pathology and lipid-mediated cellular toxicity.
Aldehyde dehydrogenase 3-A2/ALDH3A2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the ALDH3A2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the ALDH3A2 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 ALDH3A2 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 Aldehyde dehydrogenase 3-A2/ALDH3A2 protein expression.
This CRISPR knockout system enables efficient generation of ALDH3A2-deficient cell models for investigation of Aldehyde dehydrogenase 3-A2/ALDH3A2 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.