plasmid pcdna3 1 ha dnm2 k44a (ATCC)
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plasmid pcdna3 1 ha dnm2 k44a
Plasmid Pcdna3 1 Ha Dnm2 K44a, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pcdna3+1+ha+dyn2+k44a/pcDNA3%2E1HA-Dyn2+K44A/bio_rxiv__2023__06__30__547135-34-1-4
Average 92 stars, based on 9 article reviews
Plasmid Pcdna3 1 Ha Dnm2 K44a, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pcdna3+1+ha+dyn2+k44a/pcDNA3%2E1HA-Dyn2+K44A/bio_rxiv__2023__06__30__547135-34-1-4
Average 92 stars, based on 9 article reviews
plasmid pcdna3 1 ha dnm2 k44a - by Bioz Stars,
2026-09
92/100 stars
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Dominant Negative Mutation:Article Title: Peroxisome Proliferator-Activated Receptor Gamma Enhances the Activity of an Insulin Degrading Enzyme-Like Metalloprotease for Amyloid-β Article Snippet: Peroxisome proliferator-activated receptor gamma (PPARγ) activation results in an increased rate of amyloid-β (Aβ) clearance from the media of diverse cells in culture, including primary neurons and glial cells.. Here, we further investigate the mechanism for Aβ clearance and found that PPARγ activation modulates a cell surface metalloprotease that can be inhibited by metalloprotease inhibitors, like EDTA and phenanthroline, and also by the peptide hormones insulin and glucagon.. The metalloprotease profile of the Aβ-degrading mechanism is surprisingly similar to insulin-degrading enzyme (IDE). Construct:Article Title: Peroxisome Proliferator-Activated Receptor Gamma Enhances the Activity of an Insulin Degrading Enzyme-Like Metalloprotease for Amyloid-β Article Snippet: Peroxisome proliferator-activated receptor gamma (PPARγ) activation results in an increased rate of amyloid-β (Aβ) clearance from the media of diverse cells in culture, including primary neurons and glial cells.. Here, we further investigate the mechanism for Aβ clearance and found that PPARγ activation modulates a cell surface metalloprotease that can be inhibited by metalloprotease inhibitors, like EDTA and phenanthroline, and also by the peptide hormones insulin and glucagon.. The metalloprotease profile of the Aβ-degrading mechanism is surprisingly similar to insulin-degrading enzyme (IDE). |