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  • 产品名称:UBAP2L 抗原(重组蛋白)

  • 产品型号:100ug
  • 产品厂商:通蔚生物
  • 产品价格:800
  • 产品库存:35
  • 产品文档:
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简单介绍:
UBAP2L 抗原(重组蛋白)为了适应市场需要和长远发展,近年来,引进相关技术专业人才和消化国外先进的技术,不断进行产品和技术的更新改进,同时,完善的质量保证体系,提高企业的整体管理水平,一切努力和付出,惟愿助您一臂之力。
详情介绍:
中文名称: UBAP2L 抗原(重组蛋白)

英文名称: UBAP2L Antigen (Recombinant Protein)

别     名:  ubiquitin associated protein 2-like; NICE-4

储     存:  冷冻(-20℃)

相关类别: 抗原

概     述

Fusion protein corresponding to C terminal 200 amino acids of human UBAP2L

技术规格

Full name:

ubiquitin associated protein 2-like

Synonyms:

NICE-4

Swissprot:

Q14157

Gene Accession:

BC003170

Purity:

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

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

UBAP2L, also known as NICE4, is a protein that is ubiquitously expressed. Phosphorylated upon DNA damage, NICE4 contains one UBA domain and is expressed as 4 isoforms produced by alternative splicing events. The gene that encodes NICE4 maps to human chromosome 1. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.







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