FOXP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2721382

Produktdetails

Target: FOXP2 (Forkhead Box P2 (FOXP2))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses FOXP2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human FOXP2 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: 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.

Antigendetails

Target: FOXP2 (Forkhead Box P2 (FOXP2))

Andere Bezeichnung: Foxp2 (FOXP2 Produkte)

Synonyme: 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

Hintergrund: 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].

Molekulargewicht: 79.7 kDa

NCBI Accession: NP_055306