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. 2017 Dec 14;8:2120. doi: 10.1038/s41467-017-02214-8

Table 1.

Efficiency of transgenesis with different reporter constructs and treatments

Reporter Injected line Injected DNA Irradiation treatment Injected eggs Positive hatchlings (%) Germline transmission (%) Established lines
EFA::eGFP DV1 PCR 269 39 (14.50) 5 (1.86) NL1
EFA::oGFP DV1 Plasmid 114 28 (24.56) 0
EFA::oGFP DV1 Plasmid 2.5 Gy 42 13 (30.95) 2 (4.76)
EFA::oGFP DV1 Fragment 2.5 Gy 102 4 (3.92) 2 (1.96) NL7
EFA::oCherry DV1 Plasmid 2.5 Gy 80 4 (5.00) 1 (1.25) NL3
EFA::oCherry DV1 Fragment 2.5 Gy 36 6 (16.67) 3 (8.33) NL4, NL5, NL6
EFA::H2B::oGFP DV1 Fragment 2.5 Gy 38 10 (26.32) 2 (5.26) NL20
ELAV4::oGFP DV1 Fragment 2.5 Gy 56 29 (51.79) 2 (3.57) NL21
MYH6::oGFP DV1 Fragment 2.5 Gy 103 13 (12.62) 1 (0.97) NL9
APOB::oGFP DV1 Fragment 2.5 Gy 65 2 (3.08) 1 (1.54) NL22
CABP7::oGFP DV1 Plasmid 20 2 (10.00) 1 (5.00) NL23
CABP7::oNeon Green; ELAV4:: oScarlet-I NL10 Plasmid 137 3 (2.19) 2 (1.46) NL24