A collection of control elements and fluorescent reporters that can be used in combination with the MoClo-YTK toolkit for protein expression and secretion in yeast (Pichia pastoris).

Portal protein from Escherichia coli NCTC9020 prophage

Portal protein from Escherichia coli M885 prophage

Large terminase from Escherichia coli NCTC9020 prophage

Large terminase from Escherichia coli M885 prophage

Expresses LshCas13a for bacterial expression and contains backbone for spacer cloning

Expresses LwCas13a for bacterial expression and contains backbone for spacer cloning

Expresses Lw2Cas13a for bacterial expression and contains backbone for spacer cloning

A plasmid with IFP2.0 coding sequence coded into it. Expresses IFP2.0 with N-term His-tag.

A plasmid with UnaG coding sequence cloned into it. UnaG gene codon optimized for E. coli and B. theta. Expresses UnaG with N-term maltose-binding protein (MBP)-tag and C-term His-tag.

Ready-to-use AAV5 particles produced from pAAV-flex-taCasp3-TEVp (#45580). In addition to the viral particles, you will also receive purified pAAV-flex-taCasp3-TEVp plasmid DNA. EF1a-driven, Cre-dependent, bicicstronic expression of designer pro-taCasp3 and TEVp. These AAV preparations are suitable purity for injection into animals.

Ready-to-use AAV PHP.eB particles produced from CN1851-rAAV-hI56i-minBglobin-iCre-4X2C-WPRE3-BGHpA (#164450). In addition to the viral particles, you will also receive purified CN1851-rAAV-hI56i-minBglobin-iCre-4X2C-WPRE3-BGHpA plasmid DNA. minBetaGlobin-driven expression of Cre in forebrain GABAergic interneurons. For use in combination with Cre-dependent transgenic mouse lines or co-infection with Cre dependent viral vectors. These AAV were produced with the PHPeB serotype, which permits efficient transduction of the central nervous system. These AAV preparations are suitable purity for injection into animals.