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IFNAR2 (C-6His), Human, Recombinant

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产品概述

产品信息

别名Interferon Alpha/ Beta Receptor 2; IFN-R-2; IFN-Alpha Binding Protein; IFN-Alpha/ Beta Receptor 2; Interferon Alpha Binding Protein; Type I Interferon Receptor 2; IFNAR2; IFNABR; IFNARB
物种Human
表达宿主Human Cells
序列信息Ile27-Lys243
检索号P48551
分子量25.8 kDa
表观分子量46 kDa
标签C-6His
生物活性 Testing in progress

产品特性

纯度>95% as determined by reducing SDS-PAGE.
内毒素< 1.0 EU per μg as determined by LAL test.
保存Lyophilized Protein should be stored at < -20℃, though stable at room temperature for 3 weeks. Reconstituted Protein solution can be stored at 4-7℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
运输The product is shipped at ambient temperature.Upon receipt, store it immediately at the temperature listed below.
制剂Lyophilized from a 0.2 μm filtered solution of 20mM PB, 150mM NaCl, pH 7.2.
复融Please refer to it for detailed information.

背景介绍

Interferon α/ β Receptor 2 (IFN-α/ β R2) is a single-pass type I membrane Protein which belongs to the type II Cytokine Receptor family. It complexes with IFN-α/ β R1 to form the signaling Receptor complex for the family of α and β IFN subtypes. By alternative splicing, IFN-α/ β R2 can exist as a secreted soluble Protein or as a type I membrane Protein. IFN-α/ β R2 is the principal Ligand binding subunit of the Receptor. Ligand binding is stabilized by the subsequent association with IFN-α/ β R1, resulting in the formation of a signaling ternary Receptor complex. IFNAR2 was detected in most lymphocytes, monocytes, and granulocytes, although IFNAR2 expression was higher in the monocytes and granulocytes than in the lymphocytes. Among the lymphocyte subsets, IFNAR2 showed high expression in natural killer (NK) cells and low expression in T lymphocytes. Isoform 1 and isoform 3 of IFNAR2 are directly involved in signal transduction due to their interaction with the TYR kinase, JAK1. Isoform 1 also interacts with the transcriptional factors, STAT1 and STAT2. Both forms are potent inhibitors of type I IFN activity.
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