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  • 產(chǎn)品名稱：ATXN1抗原（重組蛋白）

  • 產(chǎn)品型號：1mg
  • 產(chǎn)品廠商：通蔚生物
  • 產(chǎn)品價格：3580
  • 產(chǎn)品庫存：35
  • 產(chǎn)品文檔：
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簡單介紹：
ATXN1抗原（重組蛋白）自成立以來，就注重企業(yè)信息化的建設(shè)，主要用于科研實驗使用，采用了先進(jìn)的內(nèi)部供應(yīng)鏈信息處理平臺，保證客戶訂單的準(zhǔn)確、高效處理，客戶關(guān)系的管理系統(tǒng)和客戶關(guān)系管理團(tuán)隊，能時間響應(yīng)客戶的售前、售后需求。
詳情介紹：
中文名稱： ATXN1抗原（重組蛋白）

英文名稱： ATXN1 Antigen (Recombinant Protein)

別     名：  ATX1; SCA1; D6S504E

儲     存：  冷凍（-20℃）

相關(guān)類別： 抗原

概     述：

Fusion protein corresponding to C terminal 270 amino acids of human ATXN1

技術(shù)規(guī)格

Full name:

ataxin 1

Synonyms:

ATX1; SCA1; D6S504E

Swissprot:

P54253

Gene Accession:

BC117125

Purity:

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

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions.





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