Erythropoietin (EPO) (EPO/1368), 0.2mg/mL, Clone: [EPO/1368], Mouse, Monoclonal

Artikelnummer: BOT-BNUB1368-100
Artikelname: Erythropoietin (EPO) (EPO/1368), 0.2mg/mL, Clone: [EPO/1368], Mouse, Monoclonal
Artikelnummer: BOT-BNUB1368-100
Hersteller Artikelnummer: BNUB1368-100
Alternativnummer: BOT-BNUB1368-100-100UL
Hersteller: Biotium
Wirt: Mouse
Kategorie: Antikörper
Applikation: IHC, WB
Spezies Reaktivität: Human
Immunogen: Recombinant fragment of human EPO protein (aa28-162) (exact sequence is proprietary)
Alternative Synonym: EP, EPO alpha, EPO, Epoetin, Erythropoietin, MVCD2
This antibody recognizes a protein of about 37 kDa, which is identified as Erythropoietin (EPO). Erythropoietin is a secreted, glycosylated cytokine hormone composed of four alpha helical bundles. It is the primary factor responsible for regulating erythropoiesis during steady-state conditions and in response to blood loss and hemorrhage in the adult organism. Erythropoietin is synthesized by the kidney and stimulates the proliferation and maturation of bone marrow erythroid precursor cells. The protein is found in the plasma and regulates red cell production by promoting erythroid differentiation and initiating hemoglobin synthesis.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Klonalität: Monoclonal
Konzentration: 0.2 mg/mL
Klon-Bezeichnung: [EPO/1368]
Molekulargewicht: 37 kDa
UniProt: P01588
Puffer: PBS, 0.05% BSA, 0.05% azide
Quelle: Animal
Anwendungsbeschreibung: Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Immunofluorescence: 1-2 ug/mL|Immunohistology (formalin) 4-8 ug/mL|Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 min|Flow Cytometry 0.5-1 ug/million cells/0.1 mL|Western blotting 0.5-1 ug/mL|Optimal dilution for a specific application should be determined by user