pmos blue blunt end vector system (Danaher Inc)
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Danaher Inc
pmos blue blunt end vector system
Pmos Blue Blunt End Vector System, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pmos+blue+blunt+end+vector+system/pm21126578-90-57-63
Average 86 stars, based on 1 article reviews
Pmos Blue Blunt End Vector System, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pmos+blue+blunt+end+vector+system/pm21126578-90-57-63
Average 86 stars, based on 1 article reviews
pmos blue blunt end vector system - by Bioz Stars,
2026-11
86/100 stars
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Amplification:Article Title: Vertical distribution of bacteria in a lake sediment from Antarctica by culture-independent and culture-dependent approaches. Article Snippet: .. Construction of the 16S rRNA gene library The 16S rRNA gene was amplified using the two primers 16S3 (50-TCC TAC GGG AGG CAG CAG-30) and 16S4 (50- GGC GGT GTG TAC AAG GCC C-30) as described earlier (Pradhan et al., 2010) and the amplified DNA fragments purified as above using Qiagen gel columns, and cloned into the Purification:Article Title: Vertical distribution of bacteria in a lake sediment from Antarctica by culture-independent and culture-dependent approaches. Article Snippet: .. Construction of the 16S rRNA gene library The 16S rRNA gene was amplified using the two primers 16S3 (50-TCC TAC GGG AGG CAG CAG-30) and 16S4 (50- GGC GGT GTG TAC AAG GCC C-30) as described earlier (Pradhan et al., 2010) and the amplified DNA fragments purified as above using Qiagen gel columns, and cloned into the Clone Assay:Article Title: Vertical distribution of bacteria in a lake sediment from Antarctica by culture-independent and culture-dependent approaches. Article Snippet: .. Construction of the 16S rRNA gene library The 16S rRNA gene was amplified using the two primers 16S3 (50-TCC TAC GGG AGG CAG CAG-30) and 16S4 (50- GGC GGT GTG TAC AAG GCC C-30) as described earlier (Pradhan et al., 2010) and the amplified DNA fragments purified as above using Qiagen gel columns, and cloned into the Plasmid Preparation:Article Title: Vertical distribution of bacteria in a lake sediment from Antarctica by culture-independent and culture-dependent approaches. Article Snippet: .. Construction of the 16S rRNA gene library The 16S rRNA gene was amplified using the two primers 16S3 (50-TCC TAC GGG AGG CAG CAG-30) and 16S4 (50- GGC GGT GTG TAC AAG GCC C-30) as described earlier (Pradhan et al., 2010) and the amplified DNA fragments purified as above using Qiagen gel columns, and cloned into the |