This is a Validated Antibody Database (VAD) review about human APBA1, based on 3 published articles (read how Labome selects the articles), using APBA1 antibody in all methods. It is aimed to help Labome visitors find the most suited APBA1 antibody.
APBA1 synonym: D9S411E; LIN10; MINT1; X11; X11A; X11ALPHA; amyloid beta A4 precursor protein-binding family A member 1; adapter protein X11alpha; adaptor protein X11alpha; amyloid beta (A4) precursor protein-binding, family A, member 1 (X11); mint-1; neuron-specific X11 protein; neuronal munc18-1-interacting protein 1; phosphotyrosine-binding/-interacting domain (PTB)-bearing protein
Synaptic Systems
not indicated |
| SySy Munc18 antibody was used for western blot in order to investigate the role of sphingolipids in the regulation of synaptic vesicle control. | PLoS ONE (2009) ncbi |
EMD Millipore
not indicated |
| Chemicon anti-Mint1 antibody was used to perform immunohistochemistry in order to study the roles of the amyloid precursor protein in peripheral and central synaptogenesis. . | J Neurosci (2009) ncbi |
Dako
not indicated |
| Dako monoclonal anti-AA amyloid antibody was used in immunohistochemistry to study the association of hereditary lattice corneal dystrophy with corneal amyloid deposits enclosing C-terminal fragments of feratoepithelin. | Invest Ophthalmol Vis Sci (2005) ncbi |
Articles Reviewed
- Zilai Wang et al. (2009). "Presynaptic and postsynaptic interaction of the amyloid precursor protein promotes peripheral and central synaptogenesis".PMID 19726636
- Paola G Camoletto et al. (2009). "Synaptic vesicle docking: sphingosine regulates syntaxin1 interaction with Munc18".PMID 19390577
- Barbara Stix et al. (2005). "Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin".PMID 15790870
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