blunt end cloning vector pjet1 2 (Addgene inc)
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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/vector+plasmid/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/vector+plasmid/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,
2026-11
94/100 stars
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Related Articles
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 Article Title: Evolution of inwardly rectifying potassium channels and their gene expression in zebrafish embryos. Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense zebrafish kir gene clones are available through Addgene (Plasmid # 173125-173151). .. See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable 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 Article Title: Evolution of inwardly rectifying potassium channels and their gene expression in zebrafish embryos. Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense zebrafish kir gene clones are available through Addgene (Plasmid # 173125-173151). .. See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable 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 |