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  • 產(chǎn)品名稱:NKX25 抗原(重組蛋白)

  • 產(chǎn)品型號:100ug
  • 產(chǎn)品廠商:通蔚生物
  • 產(chǎn)品價格:800
  • 產(chǎn)品庫存:35
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我司專業(yè)經(jīng)銷生命科學(xué)領(lǐng)域NKX2-5 抗原(重組蛋白),有著豐富服務(wù)經(jīng)驗和深厚專業(yè)背景的團隊為您提供技術(shù)服務(wù)和支持,各種標本、種屬、具體指標齊全,檢測范圍以及試劑盒內(nèi)容及其配制,我們努力的腳步不會就此停息,我們的成績離不開廣大新老客戶的支持與厚愛,在未來的一年里,我們將更加努力,用上等的產(chǎn)品與誠摯的服務(wù)回饋廣大用戶!
詳情介紹:



中文名稱: NKX2-5 抗原(重組蛋白)

英文名稱: NKX2-5 Antigen (Recombinant Protein)

別     名:  NK2 homeobox 5; CSX; CSX1; VSD3; CHNG5; HLHS2; NKX2E; NKX2.5; NKX4-1

儲     存:  冷凍(-20℃)

相關(guān)類別: 抗原

概     述

Fusion protein corresponding to N terminal 150 amino acids of human NKX2-5

技術(shù)規(guī)格

Full name:

NK2 homeobox 5

Synonyms:

CSX; CSX1; VSD3; CHNG5; HLHS2; NKX2E; NKX2.5; NKX4-1

Swissprot:

P52952

Gene Accession:

BC025711

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 homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.






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