Source was embryos of wild-type fly line; protein produced by endogenous gene.

Under non-reducing conditions, Ten-a has an apparent molecular weight of 600 kDa, twice it\'s predicted monomeric size, which suggests the formation of homodimers via disulfide bridges.

Anti-Ten-a western blot of proteins separated on SDS page under reducing or non-reducing conditions.

Source was cell extract of S2 cell line; bait produced from transfected construct; prey produced from transfected construct.

Ten-a homophilic interactions are similar in strength to Ten-m-Ten-a heterophilic interactions but much weaker than Ten-m homophilic interactions.