EpoR rabbit pAb

EpoR rabbit pAb

AO-06-ES5138-100

EpoR rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES5138
Product nameEpoR rabbit pAb
ReactivityHuman;Mouse;Rat;Monkey
ApplicationsWB;IF;ELISA
Other nameEPOR; Erythropoietin receptor; EPO-R
Size100μL
Unit price ($)248
Human gene ID2057
Human Swiss-ProtP19235
SourceRabbit
IsotypeIgG
TargetEpoR
Fields>>Cytokine-cytokine receptor interaction;>>PI3K-Akt signaling pathway;>>JAK-STAT signaling pathway;>>Hematopoietic cell lineage;>>Pathways in cancer
Gene nameEPOR
Protein nameErythropoietin receptor
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID13857
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP14753
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtQ07303
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human Epo-R. AA range:341-390
SpecificityEpoR Polyclonal Antibody detects endogenous levels of EpoR protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/40000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)65kD
BackgroundThis gene encodes the erythropoietin receptor which is a member of the cytokine receptor family. Upon erythropoietin binding, this receptor activates Jak2 tyrosine kinase which activates different intracellular pathways including: Ras/MAP kinase, phosphatidylinositol 3-kinase and STAT transcription factors. The stimulated erythropoietin receptor appears to have a role in erythroid cell survival. Defects in the erythropoietin receptor may produce erythroleukemia and familial erythrocytosis. Dysregulation of this gene may affect the growth of certain tumors. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010],
Functiondisease:Defects in EPOR are the cause of erythrocytosis familial type 1 (ECYT1) [MIM:133100]. ECYT1 is an autosomal dominant disorder characterized by increased serum red blood cell mass, elevated hemoglobin and hematocrit, hypersensitivity of erythroid progenitors to erythropoietin, erythropoietin low serum levels, and no increase in platelets nor leukocytes. It has a relatively benign course and does not progress to leukemia.,domain:Contains 1 copy of a cytoplasmic motif that is referred to as the immunoreceptor tyrosine-based inhibitor motif (ITIM). This motif is involved in modulation of cellular responses. The phosphorylated ITIM motif can bind the SH2 domain of several SH2-containing phosphatases.,domain:The box 1 motif is required for JAK interaction and/or activation.,domain:The WSXWS motif appears to be necessary for proper protein folding and thereby efficient intracellular tra
Subcellular locationCell membrane; Single-pass type I membrane protein.; [Isoform EPOR-S]: Secreted . Secreted and located to the cell surface.
ExpressionErythroid cells and erythroid progenitor cells. Isoform EPOR-F is the most abundant form in EPO-dependent erythroleukemia cells and in late-stage erythroid progenitors. Isoform EPOR-S and isoform EPOR-T are the predominant forms in bone marrow. Isoform EPOR-T is the most abundant from in early-stage erythroid progenitor cells.

Additional Images

Image 1
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Western Blot analysis of HepG2 cells using EpoR Polyclonal Antibody
Image 2
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Immunofluorescence analysis of HeLa cells, using Epo-R Antibody. The picture on the right is blocked with the synthesized peptide.
Image 3
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Western blot analysis of lysates from COS7 cells, treated with EPO 20U/ml 15', using Epo-R Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES5138-100
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Hurry! only 10 items left in stock.

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