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  • 產(chǎn)品名稱:COL1A2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(jià)格:3580
  • 產(chǎn)品庫存:35
  • 產(chǎn)品文檔:
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簡單介紹:
針對不同行業(yè)的需求,我司不斷完善、更新技術(shù)和方法。COL1A2抗原(重組蛋白)在實(shí)驗(yàn)室應(yīng)用的比較廣泛,被業(yè)內(nèi)眾多的科研人士認(rèn)可和推廣。公司以上等,齊全的抗體產(chǎn)品和上等的技術(shù)團(tuán)隊(duì)得到了國家各大實(shí)驗(yàn)高校及科研單位的認(rèn)可和贊譽(yù),擁有和好的知名度和口碑。
詳情介紹:


中文名稱: COL1A2抗原(重組蛋白)

英文名稱: COL1A2 Antigen (Recombinant Protein)

儲     存:  冷凍(-20℃)

相關(guān)類別: 抗原

概     述

Fusion protein corresponding to a region derived from 1133-1366 amino acids of human COL1A2

技術(shù)規(guī)格

Full name:

collagen, type I, alpha 2

Synonyms:

OI4

Swissprot:

P08123

Gene Accession:

BC042586

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 the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.





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