產(chǎn)品中心
產(chǎn)品詳情
  • 產(chǎn)品名稱:C15orf40 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(kù)存:35
  • 產(chǎn)品文檔:
你添加了1件商品 查看購(gòu)物車
簡(jiǎn)單介紹:
C15orf40 抗原(重組蛋白)公司的服務(wù)和業(yè)務(wù)網(wǎng)絡(luò)遍及國(guó)內(nèi),在同行獲得一致好評(píng),將一直伴隨著顧客的信賴成長(zhǎng),規(guī)模和抗體種類日益擴(kuò)大和更新,一直秉承著代理上等品牌的產(chǎn)品,服務(wù)好每一位顧客,將好的科學(xué)技術(shù)和方法推薦給顧客的服務(wù)宗旨。
詳情介紹:

中文名稱: C15orf40 抗原(重組蛋白)

英文名稱: C15orf40 Antigen (Recombinant Protein)

別     名:  chromosome 15 open reading frame 40

相關(guān)類別: 抗原

儲(chǔ)      存: 冷凍(-20℃) 

概      述

Fusion protein corresponding to a region derived from 28-153 amino acids of human C15orf40


技術(shù)規(guī)格

Full name:

chromosome 15 open reading frame 40

Swissprot:

Q8WUR7

Gene Accession:

BC019820

Purity:

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

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.





姓名:
電話:
您的需求: