GABA T-1 Polyclonal Antibody, 20ul[BT-AP03420] Centrifuges Defects in ACAT1 are associated

Defects in ACAT1 are associated with 3-ketothiolase deficiency

audible alert function

resulting in the reconfiguration of cadherin-actin filament connections

Activity of the encoded protein is stimulated by the Gs alpha subunit of G protein-coupled receptors and is inhibited by protein kinase A

Family members are characterized by an extended extracellular region with a variable number of N-terminal epidermal growth factor (EGF)-like domains coupled to a TM7 domain via a mucin-like spacer domain

GABA T-1 Polyclonal Antibody, 20ul[BT-AP03420] Centrifuges Defects in ACAT1 are associatedSLC6A1 (Solute Carrier Family 6 Member 1) is a Protein Coding gene. Diseases associated with SLC6A1 include myoclonic atonic epilepsy and myoclonic astastic epilepsy. Among its related pathways are Circadian entrainment and Benzodiazepine Pathway, Pharmacodynamics. GO annotations related to this gene include neurotransmitter: sodium symporter activity and gamma aminobutyric acid: sodium symporter activity. An important paralog of this gene is SLC6A4.