北京现货重组人神经调节蛋白1β(NRG1)优惠

特别声明：本产品及我公司所售其他产品均为科研类试剂产品，严禁用于药物、医疗及其他非科研用途。

北京百奥莱博专业生产销*(代"售")北京现货重组人神经调节蛋白1β(NRG1)优惠，我公司供应的分子生物学试剂品类齐全，且具有优势价格，欢迎新老客户垂询订购。

名称：北京现货重组人神经调节蛋白1β(NRG1)优惠
品牌：百奥莱博
英文名：Recombinant Human Neuregulin-1 beta
产地：国产|进口
编号：JN1223
规格：10μg|50μg|500μg|1mg
本品由我们的大肠杆菌表达系统制备而成，目的基因编码的Thr176-Lys246表达纯化得来。

NRG1质量控制：＞95%(还原性SDS-PAGE)

NRG1制剂：冻干品

NRG1保存：
冻干蛋白置于-20℃以下可长期保存，室温条件下可稳定保存3周。
复溶蛋白溶液可在4～7℃保存2～7天，可分装后置于-20℃保存三个月。

NRG1复溶：
打开试剂管前请先离心。
复溶浓度推荐大于100 μg/ml。
冻干蛋白请溶于ddH2O。
复溶后，请根据用量分装冻存，避免反复冻融。

关于NRG1：
neuregulin-1 (heregulin-1，NRG1) is a member ofneuregulin family, which is comprised of four genes that encode a large number of secreted or membrane-bound isoforms. All family members share an EGF-like domain that interacts with the ErbB family of tyrosine kinase receptors. NRG1 isoforms can be classified into type I, type II and type III isoforms. NRG1 directs ligand for ERBB3 and ERBB4 tyrosine kinase receptors, concomitantly recruits ERBB1 and ERBB2 coreceptors, resulting in ligand-stimulated tyrosine phosphorylation and activation of the ERBB receptors. NRG proteins show distinct spatial and temporal expression patterns and play important roles during development of both the nervous system and the heart.

北京现货重组人神经调节蛋白1β(NRG1)优惠极具性价比，此外，我公司正火爆促销以下产品：

·重组人凝血因子IX
编号：JN1279
英文名称：Recombinant Human Coagulation factor IX
规格：10μg|50μg|500μg|1mg
本品由我们的哺乳动物细胞表达系统制备而成，目的基因编码的Thr29-Thr461在C端含有His标签。

Coagulation factor IX质量控制：＞95%(还原性SDS-PAGE)

Coagulation factor IX制剂：液体

Coagulation factor IX保存：收到货后请置于-20℃，可保存6个月，避免反复冻融。

关于Coagulation factor IX：
Coagulation factor IX(F9), is a member of the peptidase S1 family. It contains two EGF-like domains, a Gla domain and a peptidase S1 domain. It is primarily expressed in the liver and secreted in plasma. Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca2+ ions, phospholipids, and factor VIIIa. Mutations in position 43 and 46 prevents cleavage of the propeptide, mutation in position 93 probably fails to bind to cell membranes, mutation in position 191 or in position 226 prevent cleavage of the activation peptide. Mutations of human F9 can result in thrombophilia and recessive X-linked hemophilia B (HEMB). An X-linked blood coagulation disorder characterized by a permanent tendency to hemorrhage, due to factor IX deficiency. It is phenotypically similar to hemophilia A, but patients present with fewer symptoms. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma.


北京现货重组人神经调节蛋白1β(NRG1)优惠关键词：重组神经调节蛋白1β,重组人NRG1,重组人神经调节蛋白1β蛋白,JN1223

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北京现货重组人神经调节蛋白1β(NRG1)优惠关键词：重组神经调节蛋白1β,重组人NRG1,重组人神经调节蛋白1β蛋白,JN1223

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