FTL Antikörper (Light Chain)

Produktnummer ABIN5706159

Dieses Anti-FTL-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von FTL in WB, IHC, ELISA, IF und IP. Geeignet für Human, Maus und Ratte.

Kurzübersicht für FTL Antikörper (Light Chain) (ABIN5706159)

Target: FTL (Ferritin, Light Polypeptide (FTL))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FTL Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)

Produktdetails anti-FTL Antikörper

Bindungsspezifität: Light Chain

Immunogen: ferritin, light polypeptide

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Kommentare:

human placenta tissue were subjected to SDS PAGE followed by western blot with FNab03079(FTL antibody) at dilution of 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Details zu FTL

Target: FTL (Ferritin, Light Polypeptide (FTL))

Andere Bezeichnung: Ferritin light chain

Hintergrund: Synonyms:Ferritin L subunit, Ferritin light chain, ferritin, light polypeptide, FTL Background:This gene encodes the light subunit of the ferritin protein. Ferritin is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in this light chain ferritin gene are associated with several neurodegenerative diseases and hyperferritinemia-cataract syndrome. This gene has multiple pseudogenes.

Molekulargewicht: 20-22 kDa

Pathways: Transition Metal Ion Homeostasis