Simple Commercial Access To Powerful Precision Cas-CLOVER Gene Editing And Stable piggyBac® Protein Production Technologies

Browse and select Cas-CLOVER and piggyBac reagents, or schedule a call if you would like to speak to an expert team member. Our technology is available for license fee-free research evaluation followed by commercial use options with full freedom to operate (FTO). Backed by a multi-institutional, globally issued intellectual property portfolio.

Our-Powerful-Gene-Editing-Toolbox

Demeetra's Fields of Use include Bioprocessing, Synthetic Biotechnology and Agriculture. Simply request Cas-CLOVER or piggyBac reagents below. We will send a quote, a simple evaluation agreement, protocols and can provide expert support to your team

Demeetra-Shop-Workflow-Icons-1-Order-Reagents-Gene-Editing-Technology

Order Reagents

Demeetra-Shop-Workflow-Icons-2-In-House-or-Outsource-Evaluation-Gene-Editing-Technology

Complete In-House/
Outsource Evaluation

Demeetra-Shop-Workflow-Icons-3-Commercial-License-Gene-Editing-Technology

Decide To Get A
Commercial License

Browse by system, and add reagents to your cart, and checkout at the bottom of the page:

Mammalian-icon

Mammalian Gene Editing

SKU #TECHNOLOGYDESCRIPTIONRESOURCEPRICE+
rDMT5-011Cas-CLOVER mRNACas-CLOVER mRNA: Codon optimized mRNA for mammalian systems. Use our gRNA pair design overview or Demeetra can custom design the target pairs for you (contact us below). Order gRNAs from your favorite provider and transform with the mRNA for high efficiency and clean editing.
Components: 1 vial containing 25µg of mRNA
Design Guide$650
rDMT5-027piggyBacSuper piggyBac Transposase mRNA:Codon optimized for mammalian systems. Transform cells with piggyBac mRNA and piggyBac transposon (pDMT5-028) for stable integration. Use for any cell of interest for biomanufacturing, food products, agriculture and synthetic biology
Components: 1 vial containing 25µg of mRNA
User Guide$650
rDMT5-020piggyBacExcision-Only piggyBac Transposase mRNA:Use Excision-only piggyBac transposase to remove previously integrated piggyBac transposons for phenotype reversions and Footprint-Free gene editing.
Components: 1 vial containing 25µg of mRNA
User Guide$650
pDMT5-029piggyBacSuper piggyBac Transposase Plasmid:Codon optimized for mammalian systems. Transform cells with piggyBac plasmid and piggyBac transposon (pDMT5-028) for stable integration. Use for any cell of interest for biomanufacturing, food products, agriculture and synthetic biology. Please note this plasmid is not expandable.
Components: 1 vial containing 25µg of plasmid DNA
Map

User Guide
$650
pDMT5-030piggyBacExcision-Only piggyBac Transposase DNA:Use Excision-only piggyBac transposase to remove previously integrated piggyBac transposons for phenotype reversions and Footprint-Free gene editing. Please note this plasmid is not expandable.
Components: 1 vial containing 25µg of plasmid DNA
Map

User Guide
$650
pDMT5-028piggyBacpiggyBac Transposon:Using the flexible MCS, clone in your promoter, gene and other components for optimal expression in your system. Includes ampicillin resistance.
Components: 1 vial containing 10µg of plasmid DNA
Map$350
Plant-icon

Plant Gene Editing

Plant Cas-CLOVER Gene Editing Plasmid Vector Suite: Codon optimized T-DNA based plant transformation vectors for gene knockout in plants using the Cas-CLOVER system. Expression promoters for Cas-CLOVER, gRNA’s, selection markers and other details are listed below along with links to the maps.
All vectors are 5µg per vial.

PLASMID
SKU#
CODON OPTIMIZATIONCAS-CLOVER PROMOTERGRNA PROMOTERHOST SELECTIONBACTERIAL SELECTIONPLASMID NOTESMAP LINKPRICE+
pDMT1-1A. thalianaCaMV35SOsU3HygromycinKanamycinSequential cloning of gRNAsMap$500
pDMT3-4A. thalianaCaMV35SAtU6-26HygromycinKanamycinSequential cloning of gRNAsMap$500
pDMT1-123A. thalianaCaMV35SOsU6HygromycinKanamycinSequential cloning of gRNAsMap$500
pDMT1-112A. thalianaCaMV35SOsU3KanamycinKanamycinSequential cloning of gRNAsMap$500
pDMT1-114A. thalianaCaMV35SAtU6-26KanamycinKanamycinSequential cloning of gRNAsMap$500
pDMT1-116A. thalianaCaMV35SOsU3GlufosinateKanamycinSequential cloning of gRNAsMap$500
pDMT1-118A. thalianaCaMV35SAtU6-26GlufosinateKanamycinSequential cloning of gRNAsMap$500
Yeast-icon

Yeast Gene Editing

Yeast Cas-CLOVER Gene Editing Vector Suite: We offer a series of yeast-based shuttle vectors for the expression of a Saccharomyces cerevisiae codon optimized version of Cas-CLOVER. In this platform we have designed the plasmids such that gRNA expression is polyscistronic. Expression of the Cas-CLOVER is driven by ScRNR2 promoter, and individual guides are expressed by ScSNR52 and are liberated via an intervening tRNA.

PLASMID
SKU#
CODON OPTIMIZATIONCAS-CLOVER PROMOTERGRNA PROMOTERHOST SELECTIONHOST REPLICATIONBACTERIAL SELECTIONPLASMID NOTESMAP LINKPRICE+
pDMT1-124S. cerevisiaeScRNR2No Guide Expression CassetteLEU2CEN/ARSAmpicillinBsaI sites have been mutatedMap$500
pDMT1-125S. cerevisiaeScRNR2ScSNR52LEU2CEN/ARSAmpicillinTwo guides can be cloned via GGAMap$500
pDMT1-126S. cerevisiaeScRNR2ScSNR52URA3CEN/ARSAmpicillinTwo guides can be cloned via GGAMap$500
pDMT1-127S. cerevisiaeScRNR2ScSNR52KanRCEN/ARSAmpicillinTwo guides can be cloned via GGAMap$500
pDMT1-128S. cerevisiaeScRNR2ScSNR52HygRCEN/ARSAmpicillinTwo guides can be cloned via GGAMap$500

Yeast piggyBac Engineering Vector Suite: All vectors are 10µg of plasmid DNA.

PLASMID
SKU#
CODON OPTIMIZATIONDESCRIPTIONMAP LINKPRICE+
pDMT3-23S. cerevisiaeTaking advantage of the unique massive cargo capacity, this ~25kb piggyBac transposon vector contains all genetic components required for engineering the yeast mevalonate pathway (MVA) in a single-step for the production of a high value secondary metabolites. View data.Map$1998
pDMT4-1S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-1 has a native URA3 promoter driving a URA3 auxotrophic marker.Map$650
pDMT4-2S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-2 has a defective URA3 promoter driving a URA3 auxotrophic marker allowing for more potential integrations of the transposon cassette.Map$650
pDMT4-3S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-3 has a native LEU2 promoter driving a LEU2 auxotrophic marker.Map$650
pDMT4-4S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-4 has a defective LEU2 romoter driving a LEU2 auxotrophic marker allowing for more potential integrations of the transposon cassette.Map$650
pDMT4-5S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-5 has a native HIS3 promote driving a HIS3 auxotrophic marker.Map$650
pDMT4-6S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-6 has a defective HIS3 promoter driving a HIS3 auxotrophic marker allowing for more potential integrations of the transposon cassetteMap$650
pDMT4-7S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-7 has a native TRP1 promoter driving a TRP1 auxotrophic marker.Map$650
pDMT4-8S. cerevisiaeCustomizable piggyBac transposon vector containing a large multiple cloning site (MCS) flanked by piggyBac ITRs for integration and core insulators which protect against gene silencing. pDMT4-8 has a defective TRP1 promoter driving a TRP1 auxotrophic marker allowing for more potential integrations of the transposon cassette.Map$650

GGA = Golden Gate Assembly

Total Reagents: 0

"*" indicates required fields

Buyer Information

Shipping Address

Billing address same as shipping address

Billing Address

Demeetra's Fields of Use include Bioprocessing, Synthetic Biotechnology and Agriculture. Simply request Cas-CLOVER or piggyBac reagents below. We will send a quote, a simple evaluation agreement, protocols and can provide expert support to your team

cell

Cell-Based Bioprocessing

Cell line development, cultured meats and protein production

agriculture

Agriculture

Advanced crop trait engineering, the non-GMO way

synthetic

Synthetic Biotechnology

Harnessing the power of targeted yeast editing and stable expression

Enhance your gene editing research interests with Cas-CLOVER. The recorded webinars hosted by Genetic Engineering & Biotechnology News are available below so that you can watch the areas that apply to your research.

Tseten-Jamling

Tseten Jamling, PhD.

Scientist, BMS

Maximilian-Richter

Maximilian Richter, PhD.

Senior Scientist, Immuno-Oncology, Poseida Therapeutics