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Table 3 Primer sequences used in this study

From: A single blastocyst assay optimized for detecting CRISPR/Cas9 system-induced indel mutations in mice

Primers

Sequences (5′-3′)

Purpose

3525A

CCGAAGGTAACTGGCTTCAGCAGAGCGCAG

Optimized nuclease treatment (Figure 1)

bGpA2

AACATATGCCATATGCTGGCTGCCATGAAC

Optimized nuclease treatment (Figure 1)

5S

GCCCGAGCTGGAAGCGAGAG

CRISPR/Cas9-mediated mutation (Figure 2A-D)

6A

AAGTAGGAAGCAGCATTAAGT

CRLSPR/Cas9-mediated mutation (Figure 2A-D)

1S

CTGAGTTGTGATAGCTGGCA

CRISPR/Cas9-mediated HR (Figure 4A-C)

3S

AACGTGACCTTAGCCAAGTC

CRISPR/Cas9-niediated HR (Figure 4A-C)

2A

AGTCCAGTTGCACCAGTCCTTG

CRISPR/Cas9-mediated HR (Figure 4A-C)

4A

GTACTCATACCAGCAAGGTAG

CRISPR/Cas9-mediated HR (Figure 4A-C)

PGKL1

GTTGGCGCCTACCGGTGGATGTGGAATGTG

CRISPR/Cas9-mediated HR (Figure 4A-C)

PGKL2

TGTGQGAGGCCAGAGGCCACTIGTGTAG

CRISPR/Cas9-mediated HR (Figure 4A-C)

RbGA472S

TTCCTCCTCTCCTGACTACTCCCAGTCATA

CRISPR/Cas9-mediated FIR (Figure 4A-C)

RbGA504S

CTGTCCCTCTTCTCTTATGAAGATCCCTC

CRISPR/Cas9-mediated HR (Figure 4A-C)