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  • 產(chǎn)品名稱：WFS1 抗原（重組蛋白）

  • 產(chǎn)品型號(hào)：1mg
  • 產(chǎn)品廠商：通蔚生物
  • 產(chǎn)品價(jià)格：3580
  • 產(chǎn)品庫存：35
  • 產(chǎn)品文檔：
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簡(jiǎn)單介紹：
WFS1 抗原（重組蛋白）奉行以人為本、唯才善用，提倡人是核心資本，公平合理并創(chuàng)造性地使用人才，盡可能的給員工提供足夠的舞臺(tái)去發(fā)揮去成長，公司尊重人，尊重每一位員工的個(gè)性，依托這樣的人才觀，將進(jìn)一步完善科學(xué)合理的人力資源管理機(jī)制，造就一個(gè)良好的人才成長空間。
詳情介紹：
中文名稱： WFS1 抗原（重組蛋白）

英文名稱： WFS1 Antigen (Recombinant Protein)

別     名：  Wolfram syndrome 1 (wolframin); WFS; WFRS; WFSL; CTRCT41

相關(guān)類別： 抗原

儲(chǔ)     存：  冷凍（-20℃）
 
概     述

Fusion protein corresponding to a region derived from 691-890 amino acids of human WFS1

技術(shù)規(guī)格

Full name:

Wolfram syndrome 1 (wolframin)

Synonyms:

WFS; WFRS; WFSL; CTRCT41

Swissprot:

O76024

Gene Accession:

BC030130

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene.





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