FOXP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
Quick Overview for FOXP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2721382)
Target
See all FOXP2 ProteinsProtein Type
Origin
Source
Application
Purity
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Protein Characteristics
- Transcript Variant 1
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Purification tag / Conjugate
- This FOXP2 protein is labelled with Myc-DYKDDDDK Tag.
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Characteristics
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- Recombinant human FOXP2 (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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Forkhead Box P2 (FOXP2) (AA 1-714) protein (His tag)
custom-made FOXP2 Origin: Mouse Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
Forkhead Box P2 (FOXP2) (AA 1-715) protein (His tag)custom-made FOXP2 Origin: Human Host: HEK-293 Cells Recombinant > 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
Forkhead Box P2 (FOXP2) (AA 616-715) protein (GST tag)FOXP2 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AA, AP
Forkhead Box P2 (FOXP2) (AA 1-67) protein (GST tag)FOXP2 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AA, AP
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Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays -
Comment
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The tag is located at the C-terminal.
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Restrictions
- For Research Use only
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Concentration
- 50 μg/mL
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Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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Storage
- -80 °C
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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.
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- FOXP2 (Forkhead Box P2 (FOXP2))
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Alternative Name
- Foxp2
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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].
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Molecular Weight
- 79.7 kDa
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NCBI Accession
- NP_055306
Target
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