hy 108937 d 64131 mce (MedChemExpress)
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Hy 108937 D 64131 Mce, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nsc+15364/NSC+15364/pm40614706-670-85-87
Average 93 stars, based on 12 article reviews
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Virus:Article Title: Amyloid beta glycation leads to 1 neuronal mitochondrial dysfunction and Alzheimer’s pathogenesis through VDAC1-dependent mtDNA efflux Article Snippet: The App knock-in mouse model (App SAA KI/KI; B6.Cg-Apptm1.1Dnli/J, Jackson Lab # 034711) of Alzheimer’s disease (AD) was used which carries humanizing Aβ region R684H, F681Y, and G676R mutations, and the KM670/671NL (Swedish) mutation in exon 16 as well as the E693G (Arctic) and T714I (Austrian) mutations in exon 17 of the mouse App (amyloid beta (A4) precursor protein) gene. Recombinant:Article Title: Amyloid beta glycation leads to 1 neuronal mitochondrial dysfunction and Alzheimer’s pathogenesis through VDAC1-dependent mtDNA efflux Article Snippet: The App knock-in mouse model (App SAA KI/KI; B6.Cg-Apptm1.1Dnli/J, Jackson Lab # 034711) of Alzheimer’s disease (AD) was used which carries humanizing Aβ region R684H, F681Y, and G676R mutations, and the KM670/671NL (Swedish) mutation in exon 16 as well as the E693G (Arctic) and T714I (Austrian) mutations in exon 17 of the mouse App (amyloid beta (A4) precursor protein) gene. Injection:Article Title: Amyloid beta glycation leads to 1 neuronal mitochondrial dysfunction and Alzheimer’s pathogenesis through VDAC1-dependent mtDNA efflux Article Snippet: The App knock-in mouse model (App SAA KI/KI; B6.Cg-Apptm1.1Dnli/J, Jackson Lab # 034711) of Alzheimer’s disease (AD) was used which carries humanizing Aβ region R684H, F681Y, and G676R mutations, and the KM670/671NL (Swedish) mutation in exon 16 as well as the E693G (Arctic) and T714I (Austrian) mutations in exon 17 of the mouse App (amyloid beta (A4) precursor protein) gene. Saline:Article Title: Amyloid beta glycation leads to 1 neuronal mitochondrial dysfunction and Alzheimer’s pathogenesis through VDAC1-dependent mtDNA efflux Article Snippet: The App knock-in mouse model (App SAA KI/KI; B6.Cg-Apptm1.1Dnli/J, Jackson Lab # 034711) of Alzheimer’s disease (AD) was used which carries humanizing Aβ region R684H, F681Y, and G676R mutations, and the KM670/671NL (Swedish) mutation in exon 16 as well as the E693G (Arctic) and T714I (Austrian) mutations in exon 17 of the mouse App (amyloid beta (A4) precursor protein) gene. Mouse Assay:Article Title: Amyloid beta glycation leads to 1 neuronal mitochondrial dysfunction and Alzheimer’s pathogenesis through VDAC1-dependent mtDNA efflux Article Snippet: The App knock-in mouse model (App SAA KI/KI; B6.Cg-Apptm1.1Dnli/J, Jackson Lab # 034711) of Alzheimer’s disease (AD) was used which carries humanizing Aβ region R684H, F681Y, and G676R mutations, and the KM670/671NL (Swedish) mutation in exon 16 as well as the E693G (Arctic) and T714I (Austrian) mutations in exon 17 of the mouse App (amyloid beta (A4) precursor protein) gene. |
