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Hr dna repair template

Manufactured by TriLink

HR DNA repair template is a laboratory product designed for DNA repair research. It functions as a template for homologous recombination (HR) repair, a process essential for maintaining genomic integrity. The template can be utilized in various experimental setups requiring HR-mediated DNA repair.

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2 protocols using hr dna repair template

1

CRISPR-Cas9 Flag-Knockin Mice Generation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Flag-knockin mice were generated using CRISPR-Cas9-mediated genome editing. Guide RNA was designed and ordered from Synthego (Redwood City, California, USA), guide for flag-knockin mice (5´ ACGTTTGGCACTAAGCTCTT AGG 3´). Homologous recombination (HR) DNA repair template was ordered from Integrated DNA Technologies (IDT, Coralville, Iowa, USA), template for flag-knockin mice (5´TCTGCATGTGGTTTTTATGGGGTTTTCCTTCATCGTTCTTTGTGAATCTCCTAAGAGCTGACTACAAAGACCATGACGGTGATTATAAAGATCATGACATCGATTACAAGGATGACGATGACAAGGCTTAGTGCCAAACGTATCCTAGGGAAACAGGTAGCTTGTTTTCTAAAAAGCTTGAGTAGAAA3´). Embryo microinjection into FVBxB62J F1 hybrid zygotes was performed as previously described27 (link), using 50 ng/ul of sgRNA, 25 ng/ul of HR DNA repair template, 50 ng/ul of Cas9 mRNA (TriLink Biotechnologies) and 50 ng/ul of Cas9 HiFi protein (IDT). We genotyped the flag-knockin mice using the primer sets, loci12F430, 5´GTCAGTGCTCACTTGGGATATG3´, and Flag_Rev, 5ĆCTTGTCATCGTCATCCTTGTA3´, which yield a 390bp amplicon.
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2

CRISPR-Cas9 Flag-Knockin Mice Generation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Flag-knockin mice were generated using CRISPR-Cas9-mediated genome editing. Guide RNA was designed and ordered from Synthego (Redwood City, California, USA), guide for flag-knockin mice (5´ ACGTTTGGCACTAAGCTCTT AGG 3´). Homologous recombination (HR) DNA repair template was ordered from Integrated DNA Technologies (IDT, Coralville, Iowa, USA), template for flag-knockin mice (5´TCTGCATGTGGTTTTTATGGGGTTTTCCTTCATCGTTCTTTGTGAATCTCCTAAGAGCTGACTACAAAGACCATGACGGTGATTATAAAGATCATGACATCGATTACAAGGATGACGATGACAAGGCTTAGTGCCAAACGTATCCTAGGGAAACAGGTAGCTTGTTTTCTAAAAAGCTTGAGTAGAAA3´). Embryo microinjection into FVBxB62J F1 hybrid zygotes was performed as previously described27 (link), using 50 ng/ul of sgRNA, 25 ng/ul of HR DNA repair template, 50 ng/ul of Cas9 mRNA (TriLink Biotechnologies) and 50 ng/ul of Cas9 HiFi protein (IDT). We genotyped the flag-knockin mice using the primer sets, loci12F430, 5´GTCAGTGCTCACTTGGGATATG3´, and Flag_Rev, 5ĆCTTGTCATCGTCATCCTTGTA3´, which yield a 390bp amplicon.
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