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Controls somatic sexual differentiation.
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doublesex is required in the TN1A neurons during development to increase the density of the TN1A arbors that interact with dendrites of the hg1 motoneuron.
The Flavin-containing monooxygenase-2 (Fmo-2 (show FMO2 Antibodies)) gene, a likely direct dsx target, was investigated to elucidate how sexually dimorphic expression and its evolution are brought about.
DSX targets include transcription factors and signaling pathway components providing for direct and indirect regulation of sex-biased expression
Silencing doublesex expressing neurons makes females unreceptive to courtship and copulation.
These results reveal a process that builds, via dsx(M) and social experience, the potential for a more flexible sexual behavior, which could be evolutionarily conserved as dsx-related genes that function in sexual development are found throughout the animal kingdom.
male-like pattern of SCR expression is independent of dsx function, and dsx F must be responsible for bringing about dimorphism in SCR expression, whereas dsx M function is required with Scr for the morphogenesis of sex comb.
The respective sex-specific product of the gene doublesex promotes programmed cell death of terminal neuroblasts in females, and is needed for their survival, but not proliferation, in males.
These results suggest that the foreleg provides a unique opportunity for examining the context-dependent functions of DSX.
dsx protein is required to induce female postmating behavioral responses
Dsx is a transcriptional target of Abdominal-B, and its regulation sculpts sex-specific abdomen morphology.
Controls somatic sexual differentiation. Binds directly and specifically to the FBE (fat body enhancer) of the yolk protein 1 and 2 genes (Yp1 and Yp2). This enhancer is sufficient to direct the female-specific transcription characteristic of the Yp genes in adult fat bodies. Involved in regulation of male- specific expression of takeout in brain-associated fat body.