CRISPR Insertion or Deletion Detection System

IndelCheck™ CRISPR/TALEN insertion or deletion detection system
Includes target site PCR kit (IC003) and T7 endonuclease I assay kit (IC005)
IndelCheck™ CRISPR/TALEN insertion or deletion detection system
Includes target site PCR kit (IC004) and T7 endonuclease I assay kit (IC006)
Target site PCR Kit (version 2.0)
PCR reagents for amplifying region flanking CRISPR/TALEN target site, prior to T7 Endonuclease I digestion*
Target site PCR Kit (version 2.0)
PCR reagents for amplifying region flanking CRISPR/TALEN target site, prior to T7 Endonuclease I digestion*
T7 endonuclease I assay kit
Cleave mismatched PCR products using T7 endonuclease I to detect indel mutations
T7 endonuclease I assay kit
Cleave mismatched PCR products using T7 endonuclease I to detect indel mutations
Smart-Join™ Target Site PCR Cloning Kit
Smart-Join™ Target Site PCR Cloning Kit, 20 reaction
Smart-Join™ Target Site PCR Cloning Kit
Smart-Join™ Target Site PCR Cloning Kit, 100 reaction

IndelCheck™ CRISPR/TALEN insertion or deletion detection system IndelCheck™ CRISPR/TALEN insertion or deletion detection system Target site PCR Kit (version 2.0) Target site PCR Kit (version 2.0) T7 endonuclease I assay kit T7 endonuclease I assay kit Smart-Join™ Target Site PCR Cloning Kit Smart-Join™ Target Site PCR Cloning Kit

Price: $206.00 $622.00 $159.00 $479.00 $99.00 $299.00 $249.00 $699.00
Catalog#:
  • IC001
  • IC002
  • IC003
  • IC004
  • IC005
  • IC006
  • IC007
  • IC008
Size: 50 rxns 200 rxns 50 rxns 200 rxns 50 rxns 200 rxns 20 reaction 100 reaction
Qty:
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Product Information

GeneCopoeia’s IndelCheck™ CRISPR insertion or deletion (indel) detection system provides a powerful means for assisting you in your genome editing applications. The IndelCheck™ system can be used for:

  • CRISPR sgRNA functional validation (Figure 1) before undertaking long genome editing projects (3-6 months for genome edited cell lines, or 6-9 months for genome-edited mouse lines), saving you a great deal of time and effort by eliminating CRISPR sgRNAs with poor cleavage efficiency.
  • Screening cell clones for knockout (KO) and knock-in (KI) modifications (Figure 2).

Advantages

  • Complete system to simplify your CRISPR validation and edited clone screening
  • Robust amplification for the target site PCR. No genomic DNA isolation is required
  • Easy to use T7 endonuclease I assay with optimized conditions and positive control