FGF13 Antikörper
-
- Target Alle FGF13 Antikörper anzeigen
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
-
Reaktivität
- Human, Ratte, Maus
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser FGF13 Antikörper ist unkonjugiert
-
Applikation
- Western Blotting (WB), Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human FGF13 (NP_004105.1).
- Isotyp
- IgG
- Top Product
- Discover our top product FGF13 Primärantikörper
-
-
- Applikationshinweise
- WB 1:500-1:2000 IHC 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
-
- Target
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
- Andere Bezeichnung
- FGF13 (FGF13 Produkte)
- Synonyme
- FGF13 antikoerper, fgf2 antikoerper, fhf2 antikoerper, fgf13 antikoerper, FGF-13 antikoerper, xFGF13 antikoerper, FGF2 antikoerper, FHF-2 antikoerper, FHF2 antikoerper, Fhf2 antikoerper, zgc:101784 antikoerper, fibroblast growth factor 13 antikoerper, fibroblast growth factor 13 L homeolog antikoerper, fibroblast growth factor 13a antikoerper, FGF13 antikoerper, fgf13 antikoerper, fgf13.L antikoerper, Fgf13 antikoerper, fgf13a antikoerper
- Hintergrund
- 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' end results in several transcript variants encoding different isoforms with different N-termini.
- Molekulargewicht
-
Observed_MW: 28 kDa
Calculated_MW: 21 kDa/22 kDa/25 kDa/27 kDa/28 kDa
- Gen-ID
- 2258
- UniProt
- Q92913
- Pathways
- Regulation of Cell Size
-