human FOXP2 Over-expression AAV
Category: AAV > Over-Expression
Cat. No: AAV-209278
Availability:
3-5 weeks
Name:
AAV-h-FOXP2
This is an AAV expressing Human FOXP2.
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Viral Details
- Viral Backbone
- Recombinant AAV
- AAV-ITR
- AAV2
- AAV Serotype
- Available in AAV1, AAV2, AAV3, AAV5, AAV6, AAV8, AAV9, AAV-DJ, AAV-DJ8, AAV-DJ9 and other wildtype/synthetic AAV capsids
- Promoter
- CMV (default), or choose from 30 different ubiquitous or cell specific promoter
- Reporter
- none, optional GFP, CFP, YFP, RFP or mCherry
- Storage Buffer
- PBS/5% Glycerol
Gene Details
- Species
- Human
- Gene Symbol
- FOXP2
- Gene Name
- forkhead box P2
- Gene ID
- 93986
- Gene Synonyms
- CAGH44; SPCH1; TNRC10
- ORF Size
- 1872 bp
- RefSeq#
- BC143866
- Gene Description
- FOXP2 encodes 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. FOXP2 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.
- UniGene ID
- Hs.656280
- HGNC ID
- HGNC:13875
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