Erythropoietin (EPO) (EPO/1367), 0.2mg/mL, Clone: [EPO/1367], Mouse, Monoclonal

Catalog Number: BOT-BNUB1367-100
Article Name: Erythropoietin (EPO) (EPO/1367), 0.2mg/mL, Clone: [EPO/1367], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB1367-100
Supplier Catalog Number: BNUB1367-100
Alternative Catalog Number: BOT-BNUB1367-100-100UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Application: IHC
Species Reactivity: Human
Immunogen: Recombinant fragment of human EPO protein (aa28-162) (exact sequence is proprietary)
Alternative Names: 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.
Clonality: Monoclonal
Concentration: 0.2 mg/mL
Clone Designation: [EPO/1367]
Molecular Weight: 37 kDa
UniProt: P01588
Buffer: PBS, 0.05% BSA, 0.05% azide
Source: Animal
Application Notes: 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|Optimal dilution for a specific application should be determined by user