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  • 產(chǎn)品名稱:HSD17B4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:
HSD17B4抗原(重組蛋白)大部分抗體的運(yùn)輸條件是一般的運(yùn)輸過程需要1-2周的時(shí)間,所以是在4℃的條件下來完成的,4℃運(yùn)輸*主要的目的是為了避免反復(fù)凍融對抗體活性的損害(如果使用干冰運(yùn)輸,那么收到時(shí)抗體是凍起來的,為了分裝就需要解凍,這就多了一次凍融的過程),所以運(yùn)輸過程中優(yōu)良避免干冰運(yùn)輸!
詳情介紹:
中文名稱: HSD17B4抗原(重組蛋白)

英文名稱: HSD17B4 Antigen (Recombinant Protein)

別     名:  DBP; MFE-2; MPF-2; PRLTS1; SDR8C1

儲     存:  冷凍(-20℃)

相關(guān)類別: 抗原

概     述:

Fusion protein corresponding to a region derived from 484-736 amino acids of human HSD17B4

技術(shù)規(guī)格

Full name:

hydroxysteroid (17-beta) dehydrogenase 4

Synonyms:

DBP; MFE-2; MPF-2; PRLTS1; SDR8C1

Swissprot:

P51659

Gene Accession:

BC003098

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 protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8.





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