FOXP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
-
- Target See all FOXP2 Proteins
- FOXP2 (Forkhead Box P2 (FOXP2))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 1
-
Origin
- Human
-
Source
- HEK-293 Cells
- Purification tag / Conjugate
- This FOXP2 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
-
- Recombinant human FOXP2 (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product FOXP2 Protein
-
-
- Application Notes
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
-
The tag is located at the C-terminal.
- Restrictions
- For Research Use only
-
- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
-
- Target
- FOXP2 (Forkhead Box P2 (FOXP2))
- Alternative Name
- Foxp2 (FOXP2 Products)
- Synonyms
- CAGH44 Protein, SPCH1 Protein, TNRC10 Protein, 2810043D05Rik Protein, AI449000 Protein, CAG-16 Protein, D0Kist7 Protein, RGD1559697 Protein, FOXP2 Protein, spch1 Protein, cagh44 Protein, tnrc10 Protein, xlFoxP2 Protein, foxP2 Protein, foxP Protein, Foxp2 Protein, foxP2b Protein, foxp2a Protein, forkhead box P2 Protein, lmw-gs Protein, forkhead box transcription factor Protein, forkhead box P2 L homeolog Protein, FOXP2 Protein, Foxp2 Protein, foxp2 Protein, foxP2 Protein, foxp1c Protein, foxp2.L Protein
- Background
- This gene 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. 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.[provided by RefSeq, Feb 2010].
- Molecular Weight
- 79.7 kDa
- NCBI Accession
- NP_055306
-