FOXP2 Antibodies

Antibodies that detect FOXP2 can be used in several scientific applications, including Western Blot, Immunocytochemistry, Immunohistochemistry, ELISA and Flow Cytometry. These antibodies target FOXP2 in Human, Mouse and Rat samples. Our FOXP2 polyclonal, monoclonal and recombinant monoclonal antibodies are developed in Mouse, Rabbit and Goat. Find the FOXP2 antibody that fits your needs. Choose from 1 of 12 FOXP2 antibodies, which have been validated in experiments with 1 publication and 36 images featured in our data gallery.

Browse primary antibodies for WB, Flow, IHC, ICC/IF, ELISA, IP, and other applications. Antibodies with Advanced Verification data have ... View more Antibodies that detect FOXP2 can be used in several scientific applications, including Western Blot, Immunocytochemistry, Immunohistochemistry, ELISA and Flow Cytometry. These antibodies target FOXP2 in Human, Mouse and Rat samples. Our FOXP2 polyclonal, monoclonal and recombinant monoclonal antibodies are developed in Mouse, Rabbit and Goat. Find the FOXP2 antibody that fits your needs. Choose from 1 of 12 FOXP2 antibodies, which have been validated in experiments with 1 publication and 36 images featured in our data gallery.

Browse primary antibodies for WB, Flow, IHC, ICC/IF, ELISA, IP, and other applications. Antibodies with Advanced Verification data have been validated for specificity to ensure that the antibody binds to the antigen stated. If you cannot find the antibody you're looking for, contact us today to develop custom antibodies for specific targets, species and applications.

Target Information

FOXP2 is a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.

Synonyms

2810043D05Rik; AI449000; CAG repeat protein 44; CAG-16; CAGH44; D0Kist7; DKFZp686H1726; forkhead box P2; forkhead box protein P2; forkhead/winged-helix transcription factor; FOXP2; OTTHUMP00000196932; RGD1559697; SPCH1; TNRC10; trinucleotide repeat containing 10; trinucleotide repeat-containing gene 10 protein

FOXP2 Antibodies

Target Information

Synonyms

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