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Recombinant Human Erythropoietin/EPO (C-6His)
Recombinant Human Erythropoietin is produced by our Mammalian expression system and the target gene encoding Ala28-Arg193 is expressed with a 6His tag at the C-terminus. Bon Opus Cat. #C001

Recombinant Human Erythropoietin/EPO (C-6His)

SKU: C001-10ug
$74.00Price
Quantity
[{"key":"C001-50ug","value":"Backorder"},{"key":"C001-10ug","value":"Backorder"},{"key":"C001-500ug","value":"Backorder"},{"key":"C001-1mg","value":"Backorder"}]

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Endotoxin
Less than 0.1 ng/ug (1 EU/ug) as determined by LAL test.
Accession Number
P01588
Species
Human
Expression System
Human Cells
Target Sequence
Ala28-Arg193
Tag
C-His
Formulation
Lyophilized from a 0.2 um filtered solution of PBS, pH 7.4.
Packaging
Ambient
Background
Erythropoietin (EPO) is a glycoprotein hormone that is principally known for its role in erythropoiesis, where it is responsible for stimulating proliferation and differentiation of erythroid progenitor cells. Erythropoietin is a member of the EPO/TPO family. It is a secreted, glycosylated cytokine composed of four alpha helical bundles. The differentiation of CFU-E (Colony Forming Unit-Erythroid) cells into erythrocytes can only be accomplished in the presence of EPO. Physiological levels of EPO in adult mammals are maintained primarily by the kidneys, whereas levels in fetal or neonatal mammals are maintained by the liver. EPO also can exert various non-hematopoietic activities, including vascularization and proliferation of smooth muscle, neural protection during hypoxia, and stimulation of certain B cells. Genetic variation in erythropoietin is associated with susceptbility to microvascular complications of diabetes type 2. These are pathological conditions that develop in numerous tissues and organs as a consequence of diabetes mellitus. They include diabetic retinopathy, diabetic nephropathy leading to end-stage renal disease, and diabetic neuropathy.
Purity
Greater than 95% as determined by reducing SDS-PAGE.
Erythropoietin; Epoetin; EPO
Alternative Names
Wang, A. L. et al. Comparison of Glycoprotein Separation Reveals Greater Impact of Carbohydrates and Disulfides on Electrophoretic Mobility for CE-SDS versus SDS-PAGE. Journal of pharmaceutical and biomedical analysis 180, 2019
Citation
Measured in a cell proliferation assay using TF‑1 human erythroleukemic cells. The ED50 for this effect is 80-250 pg/ml.
Activity
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