Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
URL: http://www.addgene.org/168787
Proper Citation: RRID:Addgene_168787
Bacterial Resistance: Ampicillin
Defining Citation: PMID:35168324
Vector Backbone Description: Vector Backbone:pRecomb-loxp-mCherry-4Gcloningsite-lox2272-66; Vector Types:Cre/Lox, Synthetic Biology, Expression in filamentous fungi; Bacterial Resistance:Ampicillin
Comments: pRecomb-loxp-mcherry-4Gcloningsite-lox71-2272-66 (donor vector 2) is shuttle vector that supports optional transformation-associated recombination cloning in Saccharomyces cerevisiae. Donor vector 2 also contains within the floxed region four cloning sites for the expression of biosynthetic genes under strong alcohol inducible promoters, derived from the vector pYFAC-CH2. As the four-promoter multiple cloning site is flanked by EcoRI sites, donor vector 2 can also be used for cloning genomic fragments containing a BGC.
Expand AllWe found {{ ctrl2.mentions.all_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
A list of researchers who have used the resource and an author search tool
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for pRecomb-loxP-mCherry-4Gcloningsite-lox2272-66.
No alerts have been found for pRecomb-loxP-mCherry-4Gcloningsite-lox2272-66.
Source: Addgene