We narrowed to 154 results for: plasmid

Browse Addgene's collection of plasmids for the generation and study of stem cells, from iPSC generation to directed differentiation.

CRISPR plasmids for precisely editing DNA bases without inducing a DNA break.

Plasmids from the Structural Genomics Consortium (SCG), which are primarily used for determining protein 3D structure and crystallography.

CRISPR plasmids with dCas9 fused to FokI for creating double-strand breaks (DSBs).

This resource is a collaboration between the Cell Migration Consortium (CMC) and Addgene, which highlights CMC depositing labs and plasmids.

CRISPR plasmids based on Cas13 designed to precisely edit RNA targets.

CRISPR/Cas plasmids for labeling and visualization of genomic loci.

Find prime editor plasmids for (search and replace) genome editing.

Addgene's curated collection of plasmids for cancer research, organized by signaling pathway.

Addgene’s immunology collection contains plasmids for genes involved in innate and adaptive immune signaling and cell-cell communication.

Browse AAV transfer, packaging, and helper plasmids in Addgene's repository.

Empty gRNA expression vectors for insertion of custom gRNA target sequences.

CRISPR plasmids for activating or upregulating gene expression in various model organisms.

CRISPR plasmids for transcriptional repression of target genes.

Catalytically inactive CRISPR plasmids for purification of target loci.

Find plasmids for CRISPR-associated transposases (CASTs) for insertion of donor DNA.

CRISPR plasmids that create double strand breaks in DNA.

CRISPR nickase plasmids for the generation of single-strand breaks.

Overview of Addgene's viral preparation service for plasmids and pooled libraries. Viral preparation options include lentivirus and AAV.

Find materials created at Addgene, including empty backbones, control vectors, viral packaging and expression plasmids, and more.