blunt end cloning vector pjet1 2 (Addgene inc)
94
Structured Review
Addgene inc
blunt end cloning vector pjet1 2
Blunt End Cloning Vector Pjet1 2, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/blunt+end+cloning+vector+pjet1+2/NHR1-Flag+pcDNA3%2E1+(Plasmid+%2317315)/pmc12804166-56-8-12
Average 94 stars, based on 2 article reviews
Blunt End Cloning Vector Pjet1 2, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/blunt+end+cloning+vector+pjet1+2/NHR1-Flag+pcDNA3%2E1+(Plasmid+%2317315)/pmc12804166-56-8-12
Average 94 stars, based on 2 article reviews
blunt end cloning vector pjet1 2 - by Bioz Stars,
2026-09
94/100 stars
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Clone Assay:Article Title: Metabolic reprogramming of abscisic acid-producing strain Botrytis cinerea TB-31 toward terpenoid biosynthesis using a CRISPR/Cas9 ribonucleoprotein system Article Snippet: This sequence, along with the gRNA scaffold from p426-SNR52p-gRNA (Addgene number: #43803) and the B. cinerea U6 promoter, was assembled into a PU6-20 nt-gRNA scaffold construct. .. Finally, the resulting fragment was cloned into the Cloning:Article Title: Metabolic reprogramming of abscisic acid-producing strain Botrytis cinerea TB-31 toward terpenoid biosynthesis using a CRISPR/Cas9 ribonucleoprotein system Article Snippet: This sequence, along with the gRNA scaffold from p426-SNR52p-gRNA (Addgene number: #43803) and the B. cinerea U6 promoter, was assembled into a PU6-20 nt-gRNA scaffold construct. .. Finally, the resulting fragment was cloned into the Plasmid Preparation:Article Title: Metabolic reprogramming of abscisic acid-producing strain Botrytis cinerea TB-31 toward terpenoid biosynthesis using a CRISPR/Cas9 ribonucleoprotein system Article Snippet: This sequence, along with the gRNA scaffold from p426-SNR52p-gRNA (Addgene number: #43803) and the B. cinerea U6 promoter, was assembled into a PU6-20 nt-gRNA scaffold construct. .. Finally, the resulting fragment was cloned into the Amplification:Article Title: Metabolic reprogramming of abscisic acid-producing strain Botrytis cinerea TB-31 toward terpenoid biosynthesis using a CRISPR/Cas9 ribonucleoprotein system Article Snippet: This sequence, along with the gRNA scaffold from p426-SNR52p-gRNA (Addgene number: #43803) and the B. cinerea U6 promoter, was assembled into a PU6-20 nt-gRNA scaffold construct. .. Finally, the resulting fragment was cloned into the |