Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by social communication deficits and restricted/repetitive behaviors, affecting approximately 1 in 36 children. Genetic studies have converged on synaptic dysfunction (SHANK3, neurexin-neuroligin signaling), chromatin remodeling, and mTOR pathway dysregulation as core pathogenic mechanisms, informing targeted therapeutic strategies.
Research Use Only (RUO)Not intended for diagnostic or therapeutic procedures.
Fig. 1 Key pathogenic pathways and research targets. abinScience product targets highlighted in orange.
abinScience provides validated antibodies, recombinant proteins, and ELISA kits for key autism spectrum disorder research targets. All products are manufactured by our parent company AtaGenix Laboratories under ISO quality systems. Browse products below or contact us for custom antibody development.
SHANK3 — SHANK3 is a postsynaptic scaffolding protein essential for glutamatergic synapse organization. SHANK3 haploinsufficiency causes Phelan-McDermid syndrome with high ASD penetrance. Anti-SHANK3 antibodies support synaptic density quantification and gene therapy research.
→ Browse SHANK3 antibodies
mTOR Pathway (mTOR, TSC1/TSC2) — mTOR hyperactivation (via TSC1/2 loss) drives ASD in tuberous sclerosis complex. Anti-mTOR and anti-phospho-S6K antibodies enable PI3K/Akt/mTOR signaling studies and rapamycin treatment mechanism research.
→ Browse mTOR pathway antibodies & proteins
Oxytocin / Oxytocin Receptor — Oxytocin modulates social behavior and is under clinical investigation for ASD social deficits. Anti-oxytocin receptor antibodies and recombinant oxytocin support receptor expression profiling and social neuroscience research.
→ Browse oxytocin antibodies & proteins
1. Lord C, et al. Autism spectrum disorder. Lancet. 2018;392(10146):508-520. DOI
2. Bourgeron T. From the genetic architecture to synaptic plasticity in autism spectrum disorder. Nat Rev Neurosci. 2015;16(9):551-563. DOI
3. Sato A. mTOR, a potential target to treat autism spectrum disorder. CNS Neurol Disord Drug Targets. 2016;15(5):533-543. DOI
4. Parker KJ, et al. Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder. Proc Natl Acad Sci USA. 2014;111(33):12258-12263. DOI
E. coli
Q9UHK0
His173-Arg266
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
Q8NFZ4
Val43-Phe616
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
Mammalian cells
Q8NFZ4
Gln15-Ser660
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
Mammalian cells
Q8NFZ4
Gln15-Ser660
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
P51116
Leu14-Ile388
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
P30559
Glu2-Leu38&Thr333-Ala389
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
Q9UHK0
His173-Arg266
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
P51114
Met1-Ala173
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
Q06787
Met1-Val314
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)
E. coli
P78357
Pro926-Glu1190
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Homo sapiens (Human)