FGF13 Antikörper
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- Target Alle FGF13 Antikörper anzeigen
- FGF13 (Fibroblast Growth Factor 13 (FGF13))
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Reaktivität
- Human, Ratte, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FGF13 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- Immunogen
- fibroblast growth factor 13
- Isotyp
- IgG
- Top Product
- Discover our top product FGF13 Primärantikörper
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- Applikationshinweise
- Optimal working dilution should be determined by the investigator.
- Kommentare
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Transfected HEK-293 cells were subjected to SDS PAGE followed by western blot with FNab03090( FGF13 Antibody) at dilution of 1:1000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Buffer
- PBS with 0.02 % sodium azide and 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.
- Handhabung
- Avoid repeated freeze / thaw cycles.
- Lagerung
- -20 °C
- Haltbarkeit
- 12 months
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- 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
- Synonyms:FHF2 Background: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
- 28-30 kDa
- Gen-ID
- 2258
- UniProt
- Q92913
- Pathways
- Regulation of Cell Size
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