
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Heme Oxygenase 1/HMOX1 CRISPR/Cas9 KO Plasmid (m) | sc-420882 | 20 µg | $397.00 | |||
Heme Oxygenase 1/HMOX1 HDR Plasmid (m) | sc-420882-HDR | 20 µg | $445.00 |
Mouse Hmox1 encodes heme oxygenase 1 (HMOX1), an inducible, stress-responsive enzyme that catalyzes heme degradation to biliverdin, carbon monoxide, and ferrous iron, thereby coupling heme turnover to antioxidant and iron-handling programs. HMOX1 is a core effector of NRF2/KEAP1-driven cytoprotective transcriptional responses and intersects with redox homeostasis, inflammatory signaling, mitochondrial function, and ferroptosis-related lipid peroxidation pathways. By modulating cellular responses to oxidative stress, hypoxia, xenobiotics, and cytokines, HMOX1 influences macrophage polarization, endothelial activation, and tissue injury responses in models of inflammation and metabolic stress. Dysregulated Hmox1 activity is frequently studied in contexts involving oxidative damage, altered iron metabolism, and immune-mediated pathology, making it a useful node for mechanistic dissection of stress-adaptation networks.
Heme Oxygenase 1/HMOX1 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Hmox1 gene in mouse cell lines. Each plasmid in the pool co-expresses a unique sgRNA, targeting a distinct site within the Hmox1 locus, alongside the Streptococcus pyogenes Cas9 nuclease, and encodes GFP to enable fluorescent identification and enrichment of successfully transfected cells. This multi-guide strategy increases the likelihood of inducing frameshifts or deletions that produce a functional knockout, offering a more robust alternative to single-guide approaches. DSBs induced at multiple sites are resolved through non-homologous end joining (NHEJ) or, when used with the included HDR donor template, homology-directed repair (HDR) at a defined target site within the locus.
When used in conjunction with the RFP-expressing HDR donor, GFP and RFP fluorescence can be used together to distinguish transfected from edited cell populations, streamlining flow cytometry-based sorting and clone selection workflows.
For applications requiring confirmed, selectable knockout clones, Heme Oxygenase 1/HMOX1 HDR Plasmid (m) includes an HDR donor construct containing a puromycin resistance cassette (PuroR) and a red fluorescent protein (RFP) reporter, flanked by homology arms specific to a defined Hmox1 target site.
When co-transfected with Heme Oxygenase 1/HMOX1 CRISPR/Cas9 KO Plasmid (m):
The HDR donor construct features loxP sites flanking the PuroR-RFP selection cassette to allow clean marker removal following clone confirmation. Transient expression of Cre recombinase via the included Cre Vector: sc-418923 excises the cassette, leaving a minimal residual loxP site within the Hmox1 locus and eliminating potential confounding effects on downstream assays.
This two-step approach:
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.