將外源基因導入真核細胞是分子生物學研究中的一項重要技術。轉基因載體主要分為病毒載體系統和非病毒載體系統。病毒載體系統轉染效率高,是體內基因治療的主要工具,但安全性存在隱患,且有免疫原性,體內不能反復應用,制備較復雜,而且所能裝載的外源DNA大小有限,使其應用受到很大限制。非病毒載體是病毒載體的重要補充途徑,一般認為安全性高,載體一般無免疫原性,而且是基于質粒的轉染,易于組裝[1-2]。目前已有的非病毒型載體介導基因轉染的方法有裸DNA注射、磷酸鈣介導、電轉移法、陽離子脂質體及陽離子聚合物介導等。1995年,Boussif*報道了聚乙烯亞胺(polyethylenimine,PEI)可作為非病毒載體,其后,聚乙烯亞胺成為陽離子多聚物研究zui快的領域。為了研究PEI基因轉染試劑的轉染效果,本文通過PEI轉染表達綠色熒光蛋白的pEGFP質粒到293T細胞,以觀察其效果,并測定了多種因素對轉染效率的影響。
訂貨信息如下:
Polyethyleneimine, branched (50% soln. in water, MW 750,000) | 25448-500 | 8576 |
Polyethyleneimine, Linear (MW ~100,000) | 25414-2 | 1568 |
Polyethylenimine "Max", (Mw 160,000) - High Potency Linear PEI | 25439-2 | 2496 |
Polyethylenimine "Max"?, (Mw 4,000*) - High Potency Linear PEI (Equivalent to Mw ~2,500 in Free Base Form) Polyethylenimine | 24885-2 | 2496 |
Polyethylenimine "Max"?, (nominally Mw 40,000*) - High Potency Linear PEI (Equivalent to Mw 25,000 in Free Base Form) | 24765-2 | 2496 |
Polyethylenimine, branched (30% soln. in water, MW 10,000) | 17938-100 | 1920 |
Polyethylenimine, branched (30% soln. in water, MW 70,000) | 00618-100 | 1920 |
Polyethylenimine, branched (30% soln. in water, MW 70,000) | 00618-500 | 5696 |
Polyethylenimine, branched (MW 1,200) | 06088-100 | 1120 |
Polyethylenimine, branched (MW 1,200) | 06088-500 | 3728 |
Polyethylenimine, branched (MW 1,800) | 06089-100 | 1120 |
Polyethylenimine, branched (MW 1,800) | 06089-500 | 3728 |
Polyethylenimine, branched (MW 10,000) | 19850-100 | 1120 |
Polyethylenimine, branched (MW 10,000) | 19850-500 | 4704 |
Polyethylenimine, branched (MW 50,000-100,000) | 06090-100 | 1920 |
Polyethylenimine, branched (MW 50,000-100,000) | 06090-500 | 5696 |
Polyethylenimine, branched (MW 600) | 02371-100 | 1120 |
Polyethylenimine, branched (MW 600) | 02371-500 | 3728 |
Polyethylenimine, branched, permethylated, permethobromide | 21903-10 | 3392 |
Polyethylenimine, Linear (MW 2,500) | 24313-2 | 1568 |
Polyethylenimine, Linear (MW 25,000) | 23966-2 | 1568 |
Polyethylenimine, Linear (MW 250,000) | 24314-2 | 1568 |