The phrase "after testes" is grammatically correct but may not be commonly used in written English without context.
It can be used in medical or biological discussions, particularly when referring to events or processes that occur following the testes.
Example: "The hormone levels fluctuate significantly after testes development in males."
Alternatives: "following testes" or "subsequent to testes".
Consistent with the pattern observed for the tissue-enriched genes, the three placental tissues were among the tissues with the highest number of tissue-specific genes, only after testes and brain.
Similarly, in the tammar, testosterone administration to male pouch young had no visible effect on testicular structure, although oestrogen given after testes development was initiated did cause a small degree of testicular dysgenesis [ 20].
After testes had been pulverized using mortar and tamper cooled in liquid nitrogen, TRIzol® Reagent (Invitrogen, Breda, the Netherlands) was added to the material and RNA was isolated using an RNeasy Mini Kit (Qiagen, Venlo, the Netherlands) with DNase treatment according to the manufacturer's protocol with minor modifications.
After perfusion, testes were removed and postfixed in the above mentioned fixative.
After collection, testes were fixed overnight (o/n) in 4% PFA or Bouins fixative and embedded in paraffin using standard procedures the following day.
After dehydration, testes were embedded in methyl methacrylate (MMA), 2 µm sections were cut with a Leica RM 2155 microtome with a tungsten carbide D-profile microtome knife and stained with toluidine blue.
After dissection, testes were snap frozen on dry ice and stored at −70°C until analysis.
After dissection, testes were snap frozen on dry ice and stored at −70°C before analysis.
One hour after injection, testes were dissected, fixed in 4% paraformaldehyde or Bouin, paraffin embedded and sectioned.
After excision, testes were weighed to determine the gonadosomatic index (GSI; i.e., gonad mass as a proportion of total body mass).
After dissection, testes were separately stored in 200 μl of a non-activating medium (for mixture see [ 72]) for later in vitro fertilization (sperm from the left testis) and sperm morphology determination (sperm from the right testis).
