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FOX1, also known as ataxin-2-binding protein 1 (A2BP1) and RNA binding protein fox-1 homolog 1 (RBFOX1), is an RNA binding protein and alternative splicing regulator encoded by RBFOX1 in humans.1,2,3 RBFOX1 is expressed in the brain, skeletal muscle, and heart and undergoes splicing to generate tissue-specific isoforms.4 Neuron-specific FOX1 regulates alternative splicing of genes involved in neuronal development, proliferation, and maintenance.1 Mutations in RBFOX1, including exon deletion, frameshift, and copy number mutations, have been found in patients with rolandic epilepsy, autism, and schizophrenia.2,5,6 Cayman's FOX1 Monoclonal Antibody can be used for immunofluorescence (IF) and Western blot (WB) applications. The antibody recognizes FOX1 isoforms at approximately 46 and 48 kDa from human, bovine, mouse, and rat samples.
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1. RBFOX1 regulates both splicing and transcriptional networds in human neuronal development. Hum. Mol. Genet. 21(19), 4171-4186 (2012).
2. RBFOX1 and RBFOX3 mutations in rolandic epilepsy. PLoS One 8(9), e73323 (2013).
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5. Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144B(7), 869-879 (2007).
6. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat. Genet. 40(7), 880-885 (2008).