Product Name: FNBP1L/TOCA1 Polyclonal Antibody, HRP Conjugated Catalog No

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Product Name: FNBP1L/TOCA1 Polyclonal Antibody, HRP Conjugated Catalog No. : TAP01-88159R-HRP Intended Use: For Research Use Only. Not for used in diagnostic procedures. Size 100ul Concentration 1ug/ul Gene ID ISO Type Rabbit IgG Clone N/A Immunogen Range Conjugation HRP Subcellular Locations Applications WB, IHC-P Cross Reactive Species Human, Mouse, Rat Source KLH conjugated synthetic peptide derived from human FNBP1L/TOCA1 Applications with WB(1:100-1000), IHC-P(1:100-500) Dilutions Purification Purified by Protein A. Background TOCA-1 is a 605 amino acid protein that localizes to the cytoplasm and the cytoskeleton, as well as to cytoplasmic vesicles and the cell membrane, and contains one FCH domain, one REM repeat and one SH3 domain. Existing as multiple alternatively spliced isoforms, TOCA-1 interacts with CDC42 and is required for the coordination of membrane tubulation with Actin cytoskeletal reorganization during endocytosis. Additionally, TOCA-1 is involved in membrane invagination, tubule formation and Actin polymerization. The gene encoding TOCA-1 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Synonyms C1orf39; FBP1L_HUMAN; FNBP 1L; fnbp1l; Formin binding protein 1 like; Formin-binding protein 1-like; TOCA 1; Toca-1; TOCA1; Transducer of Cdc42 dependent actin assembly 1 ; Transducer of Cdc42 dependent actin assembly protein 1; Transducer of Cdc42-dependent actin assembly protein 1. Storage Aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% Gentamicin. Store at 4°C for 12 months. If unexpected results are observed which cannot be explained by variations in laboratory procedures and a problem with the reagent is suspected, contact Technical Support at [email protected] or your distributor service. .

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Discovery of the First Genome-Wide Significant Risk Loci for ADHD
bioRxiv preprint doi: https://doi.org/10.1101/145581; this version posted June 3, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Discovery of the first genome-wide significant risk loci for ADHD Ditte Demontis,1,2,3† Raymond K. Walters,4,5† Joanna Martin,5,6,7 Manuel Mattheisen,1,2,3,8,9 Thomas D. Als,1,2,3 Esben Agerbo,1,10,11 Rich Belliveau,5 Jonas Bybjerg-Grauholm,1,12 Marie Bækvad-Hansen,1,12 Felecia Cerrato,5 Kimberly Chambert,5 Claire Churchhouse,4,5,13 Ashley Dumont,5 Nicholas Eriksson,14 Michael Gandal,15,16,17,18 Jacqueline Goldstein,4,5,13 Jakob Grove,1,2,3,19 Christine S. Hansen,1,12,20 Mads E. Hauberg,1,2,3 Mads V. Hollegaard,1,12 Daniel P. Howrigan,4,5 Hailiang Huang,4,5 Julian Maller,5,21 Alicia R. Martin,4,5,13 Jennifer Moran,5 Jonatan Pallesen,1,2,3 Duncan S. Palmer,4,5 Carsten B. Pedersen,1,10,11 Marianne G. Pedersen,1,10,11 Timothy Poterba,4,5,13 Jesper B. Poulsen,1,12 Stephan Ripke,4,5,13,22 Elise B. Robinson,4,23 Kyle F. Satterstrom,4,5,13 Christine Stevens,5 Patrick Turley,4,5 Hyejung Won,15,16 ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium, 23andMe Research Team, Ole A.
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