rabbit polyclonal antibodies against gat 1 (Alomone Labs)
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rabbit polyclonal antibodies against gat 1
Rabbit Polyclonal Antibodies Against Gat 1, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+polyclonal+antibodies+against+gat+1/Anti-GABA+Transporter+1+(GAT-1)+(extracellular)+Antibody/pmc09472560-120-5-10
Average 93 stars, based on 7 article reviews
Rabbit Polyclonal Antibodies Against Gat 1, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+polyclonal+antibodies+against+gat+1/Anti-GABA+Transporter+1+(GAT-1)+(extracellular)+Antibody/pmc09472560-120-5-10
Average 93 stars, based on 7 article reviews
rabbit polyclonal antibodies against gat 1 - by Bioz Stars,
2026-10
93/100 stars
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Incubation:Article Title: Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD Article Snippet: .. Membranes were incubated with primary Article Title: Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humans. Article Snippet: .. Membranes were incubated with primary Article Title: A missense mutation in SLC6A1 associated with Lennox-Gastaut syndrome impairs GABA transporter 1 protein trafficking and function Article Snippet: .. Membranes were incubated with primary Article Title: Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism Article Snippet: .. Membranes were incubated with primary Article Title: Genetic mosaicism, intrafamilial phenotypic heterogeneity, and molecular defects of a novel missense SLC6A1 mutation associated with epilepsy and ADHD. Article Snippet: Background: Mutations in SLC6A1, encoding γ-aminobutyric acid (GABA) transporter 1 (GAT-1), have been recently associated with a spectrum of neurodevelopmental disorders ranging from variable epilepsy syndromes, intellectual disability (ID), autism and others.. To date, most identified mutations are de novo.. We here report a pedigree of two siblings associated with myoclonic astatic epilepsy, attention deficit hyperactivity disorder Article Title: Astrocytic GABA transporter 1 deficit in novel SLC6A1 variants mediated epilepsy: Connected from protein destabilization to seizures in mice and humans Article Snippet: .. Membranes were incubated with primary |