Custom Alt-R™ CRISPR-Cas9 guide RNA
Integrated DNA Technologies Inc.Use our proprietary algorithms to design custom Cas9 guide RNAs
Products, services, reviews and techniques used in the identification and validation of the disease-causing target genes and proteins.
Use our proprietary algorithms to design custom Cas9 guide RNAs
Guide RNAs (gRNAs) contain the target-specific sequence for guiding Cas9 protein to a genomic location.
Guide RNAs (gRNAs) contain the target-specific sequence for guiding Cas9 protein to a genomic location.
Guide RNAs (gRNAs) contain the target-specific sequence for guiding Cas9 protein to a genomic location.
Hybridizes to crRNA to activate the Cas9 enzyme.
Hybridizes to crRNA to activate the Cas9 enzyme.
urified carrier DNA that improves delivery of Cas9 ribonucleoprotein (RNP) by electroporation.
Purified carrier DNA that is required for efficient delivery of Cpf1 ribonucleoprotein (RNP) by electroporation.
For detection of on-target or known off-target CRISPR events in cultured cells
An advanced data analysis pipeline for quantifying your genome editing results
Highly multiplexed, targeted amplicon sequencing for critical analysis of your CRISPR edits
NGS-ready amplicon libraries. Fast. Easy. Convenient.
A small molecule compound that has demonstrated an ability to increase the rate of homology-directed repair (HDR).
Deep, targeted amplicon sequencing with highly multiplexed panels for sequencing on Illumina platforms.
DsiRNAs are 27mer duplex RNAs that demonstrate increased potency in RNA interference compared to traditional, 21mer siRNAs. Proprietary design rules produce optimized DsiRNAs that are available only from IDT.
Antisense oligonucleotides (ASOs) are short oligonucleotides that localize to the nucleus and provide a pathway for gene silencing by the RNase H pathway. Phosphorothioate (PS) linkages are available to confer nuclease resistance and, therefore, enhance intracellular stability.
These steric blocking oligonucleotides hybridize to mature miRNAs and inhibit their function.
Complete synthetic genes with 100% sequence verification are provided in a plasmid cloning vector and ready to use in a variety of applications.
Double-stranded DNA fragments for quick and cost-effective cloning
Recombinant SARS-CoV-2 Spike Protein, S1 Subunit, Host Cell Receptor Binding Domain (RBD) derived from E.coli
Recombinant SARS-CoV-2 S1 Subunit Protein with C-terminal His-tag, secreted from the serum-free medium of transfected HEK293 cells. Purchase will also include one vial of normal control (Catalog #. 230-20001), the culture supernatant of HEK293 cell transfected with empty expression vector.
Recombinant SARS-CoV-2 S1 subunit protein with C-terminal His-tag, derived from the transfected human HEK293 cells.
Recombinant SARS-CoV-2 S2 Subunit Protein with C-terminal tag, derived from the transfected human HEK293 cells.
Recombinant SARS-CoV-2 Nucleocapsid Protein with C-terminal His-tag, derived from the transfected human HEK293 cells.
Recombinant Human Angiotensin-converting Enzyme 2 (ACE2) with C-terminal His-tag, derived from the transfected human HEK293 cells.