MinElute 96 UF PCR Purification Kit

使用超滤方法高通量纯化多至15 μg PCR产物（长度小于100 bp）

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MinElute 96 UF PCR Purification Kit (4)

Cat. No. / ID: 28051

4 MinElute 96 UF PCR Purification Plates

Pieces

Inquire

MinElute 96 UF PCR Purification Kit 旨在用于分子生物学应用。该产品不能用于疾病诊断、预防和治疗。

✓ 全天候自动处理在线订单

✓ 博学专业的产品和技术支持

✓ 快速可靠的（再）订购

特点

非常小的洗脱体积
纯化速度快，操作容易
回收率高，重复性好

产品详情

MinElute 96 UF PCR Purification Kit基于超滤技术，使用96孔板，用于>100 bp的PCR产物的高通量纯化。特殊设计的板子可将DNA洗脱至非常小的体积（20 μl），获得高产、高度浓缩的DNA。该流程可在BioRobot Universal System上自动化进行。使用MinElute体系纯化的DNA片段可直接用于各种应用，包括：测序、微芯片分析、连接和转化、限制性酶切、标记、显微注射、PCR和体外转录。MinElute 96 UF PCR Purification Kit需使用QIAvac Multiwell真空装置（货号：9014579）。

绩效

MinElute 96 UF PCR Purification Kit使用96孔板高通量纯化PCR产物。在BioRobot 3000（已停产）、BioRobot 8000或BioRobot Universal System上全自动处理1–8个96孔板，或在QIAvac Multiwell Manifold（货号：9014579，需合适的真空管，如QIAvac Multiwell管，建议使用孔板振荡器）上处理1个96孔板。纯化>100 bp的DNA的回收率为80–95%。使用少量洗脱液（人工操作需20 µl，如使用BioRobot工作站则需30 µl）即可将纯化的PCR产物从膜表面洗脱下来，得到高浓度DNA（参见）用于各种下游应用。无论是人工操作还是全自动流程都可处理多达150 µl的PCR产物。

查看图表

Highly concentrated DNA eluates.

原理

QIAGEN MinElute 96 UF PCR Purification Kit设计独特，结合了多孔技术的便利性和超滤膜的高效分离特性。使用孔板可对>100 bp的双链DNA片段进行快速高效回收，并除去引物（<20mers）、未整合的核苷酸链和盐。

程序

MinElute 96 UF PCR Purification Kits运用超滤技术，在真空环境下使用QIAvac纯化PCR产物（参见""）。在真空条件下，将PCR产物上样超滤板的孔中。引物、盐和未整合的核苷酸链等小分子通过滤膜，而大于100 bp的PCR产物留下来。水、DMSO或缓冲液如SSC等可以作为洗脱液。MinElute 96 UF PCR Purification操作流程可在BioRobot 3000（已停产）、BioRobot 8000、或BioRobot Universal System上全自动进行。

查看图表

MinElute 96 UF PCR Purification procedure.

应用

MinElute 96 UF系统纯化得到的DNA片段可直接用于各种应用，包括：

测序
微阵列分析
连接和转化
限制性酶切
标记

辅助数据和图表

miScript miRNA QC PCR Array layout for plate formats E and G.

Specifications

Features	Specifications
Binding capacity	<150 µl
Recovery: oligonucleotides dsDNA	Recovery: oligonucleotides, dsDNA
Elution volume	20–30µl
Format	96-well plate
Fragment size	>100 bp
Removal <10mers 17–40mers dye terminator proteins	Removal <20mers
Technology	Ultrafiltration
Sample type: applications	DNA, oligonucleotides: PCR reactions
Processing	Manual/automated

资源

For efficient, high-throughput purification of PCR products

Publications

Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.

Pfeifer D; Pantic M; Skatulla I; Rawluk J; Kreutz C; Martens UM; Fisch P; Timmer J; Veelken H;

Blood; 2006; 109 (3):1202-10 2006 Oct 19 PMID:17053054

Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes.

Baron CA; Tepper CG; Liu SY; Davis RR; Wang NJ; Schanen NC; Gregg JP;

Hum Mol Genet; 2006; 15 (6):853-69 2006 Jan 30 PMID:16446308

Multilocus sequence typing of Staphylococcus aureus isolated from high-somatic-cell-count cows and the environment of an organic dairy farm in the United Kingdom.

Smith EM; Green LE; Medley GF; Bird HE; Dowson CG;

J Clin Microbiol; 2005; 43 (9):4731-6 2005 Sep PMID:16145134

Multilocus sequence typing of intercontinental bovine Staphylococcus aureus isolates.

Smith EM; Green LE; Medley GF; Bird HE; Fox LK; Schukken YH; Kruze JV; Bradley AJ; Zadoks RN; Dowson CG;

J Clin Microbiol; 2005; 43 (9):4737-43 2005 Sep PMID:16145135

Pooled association genome scanning: validation and use to identify addiction vulnerability loci in two samples.

Liu QR; Drgon T; Walther D; Johnson C; Poleskaya O; Hess J; Uhl GR;

Proc Natl Acad Sci U S A; 2005; 102 (33):11864-9 2005 Aug 9 PMID:16091475

FAQ

We do not recommend the use of samples containing mineral oil since mineral oil will not be removed during the purification procedure.

FAQ ID -360

Yes, you may use part of the MinElute 96 UF Plate, and use the rest of the plate later. In contrast to silica membrane based plates, the unused part of the UF plate does not need to be taped off. We do not recommend to re-use MinElute 96 UF Plates more than 2-4 times.

FAQ ID -355

Yes, please follow the User-Developed Protocol 'Concentration of RNA in 96-well plates using the MinElute 96 UF PCR Purification Kit' (RN03).

FAQ ID -1546