FGF13 Protein (Transcript Variant 6) (Myc-DYKDDDDK Tag)

N° du produit ABIN2721060

Détail du produit

Antigène: FGF13 (Fibroblast Growth Factor 13 (FGF13))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 6

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette FGF13 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human FGF13 (transcript variant 6) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

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

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

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

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

Antigène: FGF13 (Fibroblast Growth Factor 13 (FGF13))

Autre désignation: Fgf13 (FGF13 Produits)

Synonymes: FGF13 Protein, fgf2 Protein, fhf2 Protein, fgf13 Protein, FGF-13 Protein, xFGF13 Protein, FGF2 Protein, FHF-2 Protein, FHF2 Protein, Fhf2 Protein, zgc:101784 Protein, fibroblast growth factor 13 Protein, fibroblast growth factor 13 L homeolog Protein, fibroblast growth factor 13a Protein, FGF13 Protein, fgf13 Protein, fgf13.L Protein, Fgf13 Protein, fgf13a Protein

Sujet: The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5&apos end results in several transcript variants encoding different isoforms with different N-termini.

Poids moléculaire: 21.4 kDa

NCBI Accession: NP_378668

Pathways: Regulation of Cell Size