FGF13 anticorps

N° du produit ABIN2459900

Détail du produit anti-FGF13 anticorps

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

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FGF13 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FGF13.

Information d'application

Indications d'application: FGF13 antibody can be used for detection of FGF13 by ELISA at 1:62500. FGF13 antibody can be used for detection of FGF13 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store FGF13 antibody at -20 °C.

Détails sur FGF13

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

Autre désignation: FGF13 (FGF13 Produits)

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

Sujet: FGF13 is probably involved in nervous system development and function.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 to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.

Poids moléculaire: 27 kDa

ID gène: 2258

NCBI Accession: NP_004105

UniProt: Q92913

Pathways: Regulation of Cell Size