Journal: bioRxiv
Article Title: Double UP: efficient in utero electroporation via internal controls
doi: 10.1101/571323
Figure Lengend Snippet: Construction and characterization of Double UP. (a) Schematic of Double UP construct. (b) Representative IUE of Double UP without Cre (top) and with pCAG-Cre in a 75:1 molar ratio (bottom). Embryos were electroporated at E14.5 and allowed 3 days to mature (E14.5+3). Scale bar, 100µm. (c) Comparison of migration of mNeon-Green- and mScarlet-positive neurons, E14.5+3. Each dot represents mean distance from the top of the cortical plate of neurons within one slice. Connected dots indicate that those measures came from the same brain. n=10 slices with 100 - 976 neurons from each slice. No significant difference between green and red populations (two-way ANOVA). Error bars not shown for clarity. (d) Comparison of reliability of controls between section matching and Double UP. Full data in . 76 comparisons made for section matching, 61 for Double UP. Only sections that had a perfect match in another brain were included for either analysis. **** p<0.0001., Kolmogorov-Smirnov t-test, two-tailed. Lines indicate mean and SD.
Article Snippet: Double UP superfolderGFP-to-mScarlet, and Double UP mClover3-to-mScarlet are available through Addgene (Addgene #120261 and #120262).
Techniques: Construct, Migration, Two Tailed Test