calcium phosphate method13 (Thermo Fisher)
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calcium phosphate method13
Calcium Phosphate Method13, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/calcium+phosphate+method13/Phosphate/pm11698279-70-24-55
Average 99 stars, based on 1 article reviews
Calcium Phosphate Method13, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/calcium+phosphate+method13/Phosphate/pm11698279-70-24-55
Average 99 stars, based on 1 article reviews
calcium phosphate method13 - by Bioz Stars,
2026-11
99/100 stars
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Transfection:Article Title: Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins. Article Snippet: Some families affected by von Willebrand disease type 1 show high penetrance with exceptionally low von Willebrand factor (VWF) levels.. Previously, a mutation associated with this dominant phenotype, Cys1149Arg, was found to decrease the secretion of coexpressed normal VWF, and the mutation was proposed to cause intracellular retention of pro-VWF heterodimers.. To demonstrate heterodimer formation, a model was developed in which subunits could be distinguished immunologically and by size. Saline:Article Title: Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins. Article Snippet: Some families affected by von Willebrand disease type 1 show high penetrance with exceptionally low von Willebrand factor (VWF) levels.. Previously, a mutation associated with this dominant phenotype, Cys1149Arg, was found to decrease the secretion of coexpressed normal VWF, and the mutation was proposed to cause intracellular retention of pro-VWF heterodimers.. To demonstrate heterodimer formation, a model was developed in which subunits could be distinguished immunologically and by size. |