Journal: STAR Protocols
Article Title: Protocol to measure temporal consumption and feeding choices of Drosophila adults using capillaries
doi: 10.1016/j.xpro.2025.103931
Figure Lengend Snippet: Introduce flies into multiCAFE cage (A) Material needed: (1) a multiCAFE cage, (2) two microscope slides, (3) a comb, (4) a mouth aspirator, and (5) at least 8 flies as needed. (B) Introduce a microscope slide between the vertical branches of the multiCAFE cage, by sliding it in the lateral grooves up to the end. (C) Add a “comb” to prevent the slide from moving up and later to prevent flies from escaping. Flip the cage upside down so that the slide is now at the bottom of the cage. (D) Catch a fly with your aspirator. (E) Slide in a microscope slide over the first cage (that will remain empty) and with a mouth aspirator, blow out one fly in the next cage. Push quickly the microscope slide over the cage to trap the fly. Repeat the process 8 times. Note: usually, we leave empty the cells 1 and 10 (see numbers below the row of cells on the figure). (F) At the end of the process, center the slide and fix it in position with tape on each side. Eventually label each tape to remember how to place the capillaries (here “suc/caf” on the left for “sucrose versus caffeine” and “CS” on the right tab for “Canton S”).
Article Snippet: Fill the capillaries and align them on a microscope glass slide The capillaries are filled by capillarity when plunged into the solution within an Eppendorf.
Techniques: Introduce, Microscopy