cs phosphor-imaging screen (Bio-Rad)
Bio-Rad is a verified supplier 
90
Structured Review
Bio-Rad
cs phosphor-imaging screen
Cs Phosphor Imaging Screen, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cs+phosphor-imaging+screen/ChemiDoc+MP+Imaging+System/pm12080419-62-6-6
Average 90 stars, based on 1 article reviews
Cs Phosphor Imaging Screen, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cs+phosphor-imaging+screen/ChemiDoc+MP+Imaging+System/pm12080419-62-6-6
Average 90 stars, based on 1 article reviews
cs phosphor-imaging screen - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
Hybridization:Article Title: Use of degenerate primers and touchdown PCR to amplify a halogenase gene fragment from Streptomyces venezuelae ISP5230. Article Snippet: Consensus amino acid sequences of FADH2-dependent bacterial halogenases were used to design PCR primers amplifying a halogenase gene fragment from the chloramphenicol producer Streptomyces venezuelae ISP5230.. The sequence-specific degenerate primers (MPF1 and MPR2) were used with a touchdown PCR procedure in the first PCR-assisted cloning of a halogenase gene fragment.. In the region of the 290-bp PCR product containing the reverse primer, the deduced amino acid sequence exhibited characteristics of a – – fold present in FAD-binding sites of certain monooxygenases. Imaging:Article Title: Use of degenerate primers and touchdown PCR to amplify a halogenase gene fragment from Streptomyces venezuelae ISP5230. Article Snippet: Consensus amino acid sequences of FADH2-dependent bacterial halogenases were used to design PCR primers amplifying a halogenase gene fragment from the chloramphenicol producer Streptomyces venezuelae ISP5230.. The sequence-specific degenerate primers (MPF1 and MPR2) were used with a touchdown PCR procedure in the first PCR-assisted cloning of a halogenase gene fragment.. In the region of the 290-bp PCR product containing the reverse primer, the deduced amino acid sequence exhibited characteristics of a – – fold present in FAD-binding sites of certain monooxygenases. |