
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
LDH-A CRISPR Activation Plasmid (h) | sc-400403-ACT | 20 µg | $397.00 |
Human LDHA encodes lactate dehydrogenase A (LDH-A), a cytosolic enzyme that catalyzes the interconversion of pyruvate and lactate with concomitant NADH/NAD⁺ recycling, supporting glycolytic flux under aerobic and hypoxic conditions. LDH-A is a central node in glucose metabolism and redox homeostasis, influencing metabolic rewiring associated with high proliferative demand and microenvironmental hypoxia. Altered LDHA activity has been linked to changes in lactate production, intracellular pH balance, and carbon partitioning between glycolysis and mitochondrial oxidation, making it relevant to studies of metabolic regulation in cancer biology and other disorders with dysregulated energy metabolism.
LDH-A CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous LDHA expression without altering the underlying DNA sequence.
LDH-A CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the LDHA locus in human cell lines. The system is built around a catalytically inactive Cas9 (dCas9) carrying two inactivating mutations (D10A and N863A) that eliminate nuclease activity while preserving DNA binding. This dCas9 is fused to VP64, a potent transcriptional activator, and is co-expressed with a blasticidin resistance gene for selection. The second plasmid encodes the MS2-p65-HSF1 fusion protein, a secondary activator complex that works in concert with dCas9-VP64, alongside a hygromycin resistance gene. The third plasmid encodes a target-specific 20 nt sgRNA fused to two MS2 RNA aptamers that recruit the MS2-p65-HSF1 complex to the activation site, accompanied by a puromycin resistance gene. The three plasmids are delivered at a 1:1:1 mass ratio for balanced expression of all system components.
Once assembled at the target locus, the SAM complex binds within approximately 200 bp upstream of the LDHA transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous LDH-A expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native LDHA locus and enabling the study of LDH-A-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of LDH-A pathway restoration in tumor cells with silenced or reduced LDHA expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.