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TPO Polyclonal Antibody
TPO Polyclonal Antibody
TPO Polyclonal Antibody
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经销商客户: ¥440.0
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商品描述

商品属性

Target:TPO

Fields:Cytokine-cytokine receptor interaction;JAK-STAT signaling pathway;Hematopoietic cell lineage

Gene Name:THPO

Protein Name:Thrombopoietin

Human Gene Id:7066

Human Swiss Prot No:P40225

Mouse Gene Id:21832

Mouse Swiss Prot No:P40226

Rat Gene Id:81811

Rat Swiss Prot No:P49745

Immunogen:The antiserum was produced against synthesized peptide derived from the Internal region of human THPO. AA range:41-90

Specificity:TPO Polyclonal Antibody detects endogenous levels of TPO protein.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500 - 1:2000. IHC: 1:100-1:300. ELISA: 1:20000.. IF 1:50-200

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name:THPO;MGDF;Thrombopoietin;C-mpl ligand;ML;Megakaryocyte colony-stimulating factor;Megakaryocyte growth and development factor;MGDF;Myeloproliferative leukemia virus oncogene ligand

Observed Band(KD):38kD

Background: Megakaryocytopoiesis is the cellular development process that leads to platelet production. The main functional protein encoded by this gene is a humoral growth factor that is necessary for megakaryocyte proliferation and maturation, as well as for thrombopoiesis. This protein is the ligand for MLP/C_MPL, the product of myeloproliferative leukemia virus oncogene. Mutations in this gene are the cause of thrombocythemia 1. Alternative promoter usage and differential splicing result in multiple transcript variants differing in the 5' UTR and/or coding region. Multiple AUG codons upstream of the main open reading frame (ORF) have been identified, and these upstream AUGs inhibit translation of the main ORF at different extent. [provided by RefSeq, Feb 2014],

Function:disease:Defects in THPO are a cause of essential thrombocythemia (ET) [MIM:187950]. ET is inherited as an autosomal dominant trait which is characterized by elevated platelet levels due to sustained proliferation of megakaryocytes, and frequently lead to thrombotic and haemorrhagic complications.,domain:Two-domain structure with an erythropoietin-like N-terminal and a Ser/Pro/Thr-rich C-terminal.,function:Lineage-specific cytokine affecting the proliferation and maturation of megakaryocytes from their committed progenitor cells. It acts at a late stage of megakaryocyte development. It may be the major physiological regulator of circulating platelets.,similarity:Belongs to the EPO/TPO family.,

Subcellular Location:Secreted.

Expression: Brain,Fetal liver,Liver,Placenta,

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