Merck
CN

NA1020

Sigma-Aldrich

GenElute PCR 纯化试剂盒

sufficient for 70 purifications

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别名:
Gen Elute, PCR纯化
NACRES:
NA.52

用途

sufficient for 70 purifications

质量水平

technique(s)

DNA purification: suitable

储存温度

15-25°C

一般描述

GenElute PCR回收试剂盒可用于从各种其他反应组分(如多余的引物、核苷酸、DNA聚合酶、油和盐)之中快速纯化出单链或双链PCR扩增产物(长度100 bp至10 kb)。该试剂盒将硅胶结合技术的优势与传统离心柱形式结合在一起,同时无需采用昂贵的树脂或苯酚和氯仿等有毒有机化学成分。

应用

GenElute PCR产物纯化试剂盒已被用于从反应的其他组分中快速纯化单链或双链PCR扩增产物(100bp至10kb)。
纯化所得的DNA可用于酶促反应、传统或自动化测序、克隆和微阵列分析。

特点和优势

  • 可在8分钟内纯化出多达100 μl或10 μg 的PCR扩增产物DNA。
  • 可回收95%长度介于100 bp至10 kb之间的PCR产物
  • 可去除99%以上的引物和其他成分
  • 不需要去除有机萃取引入的矿物油
  • 相对于其他市场领先竞争对手,可多获得40%的纯化制备物

其他说明

GenElute PCR回收试剂盒可用于从各种其他反应组分(如多余的引物、核苷酸、DNA聚合酶、油和盐)之中快速纯化出单链或双链PCR扩增产物(长度100 bp至10 kb)。该试剂盒将硅胶结合技术的优势与传统离心柱形式结合在一起,同时无需采用昂贵的树脂或苯酚和氯仿等有毒有机化学成分。

原理

GenElute PCR回收试剂盒将硅胶结合和微量离心形式的优势结合在一起。DNA结合到离心柱内的硅胶膜上。结合所得的DNA经过洗涤后,再在所选的缓冲液中洗脱所得的洁净、浓缩的DNA。每个离心柱至多可纯化100 μL或10 μg经PCR扩增的DNA,至多可纯化出 95%的100 bp至10 kb大小的PCR产物。该试剂盒可去除99%以上的引物和大多数的引物二聚体(可去除<40 bp的片段)。

法律信息

GenElute is a trademark of Sigma-Aldrich Co. LLC

象形图

CorrosionExclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Central nervous system

储存分类代码

8A - Combustible, corrosive hazardous materials

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

危险化学品

分析证书(COA)

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示例

T1503
货号
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25G
包装规格/数量

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1000309185

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索取COA

  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. Can Product NA1020, GenElute PCR Clean-Up Kit, be used for isolation of PCR products labeled with digoxigenin?

    Although we have not tested the kit with digoxigenin-labeled PCR products specifically, it should be fine to use

  6. Can Product No. NA1020, GenElute PCR Clean-Up Kit,  be used to clean up PCR products larger than 10 kb?

    We haven't tested anything bigger than 10 kb, but we would expect larger DNA to bind well.  That said, the bound DNA might be more difficult to elute.  Heating the elution solution to 60-65°C may help with elution.  Incubating a few minutes to allow the elution solution to soak into the binding matrix may also help.

  7. When using Product No. NA1020, GenElute PCR Clean-Up Kit, what is the largest amount of PCR reaction sample that can be processed on one column?

    The upper limit on the PCR reaction volume that can be cleaned up is 100 μl. In that scenario, 500 μl of binding solution would be added for a total of 600 μl volume being applied to the column.

  8. When using GenElute PCR Clean-Up Kit, Product No. NA1020, Can the amount of elution buffer be reduced in order to obtain a more concentrated eluate?

    One may indeed increase concentration by reducing elution volume, but we would not suggest going lower than 25-30 μl. One must keep in mind that if a volume of less than 50 μl is used (for example, 30 μl), the concentration will increase, but the total yield will also be reduced.

  9. Can GenElute PCR Clean-Up Kit, Product NA1020, be used for isolation of labeled PCR products?

    This kit will work with labeled PCR products and no modifications to the standard protocol are needed.

  10. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Hashem Al-Sheikh
Saudi journal of biological sciences, 17(4), 347-352 (2010-10-01)
During a survey of pathogenic and non-pathogenic Pythium spp. in different localities in Egypt, several isolates of Pythia were obtained and maintained on corn meal agar. Among these isolates, Pythium aphanidermatum and Pythium diclinum were obtained from rhizosphere of wheat
Isolation of disseminated neuroblastoma cells from bone marrow aspirates for pretreatment risk assessment by array comparative genomic hybridization.
Vandewoestyne M
International Journal of Cancer. Journal International Du Cancer, 130(5), 1098-1108 (2012)
Najla Chabchoub et al.
The American journal of tropical medicine and hygiene, 80(1), 24-27 (2009-01-15)
Stool samples from 86 immunocompromised patients (51 human immunodeficiency virus (HIV)-infected patients and 35 patients with haematologic malignancies) were systematically screened for intestinal microspordiosis by microscopic examination and polymerase chain reaction (PCR) using universal primer V1/PMP2. Nine samples (10.5%) showed
Andreas Veith et al.
Frontiers in microbiology, 2, 37-37 (2011-07-13)
The sulfur oxygenase reductase (SOR) is the initial enzyme of the sulfur oxidation pathway in the thermoacidophilic Archaeon Acidianus ambivalens. The SOR catalyzes an oxygen-dependent sulfur disproportionation to H(2)S, sulfite and thiosulfate. The spherical, hollow, cytoplasmic enzyme is composed of
Kathleen Gärtner et al.
Retrovirology, 6, 32-32 (2009-04-08)
Foamy viruses (FVs) are the most genetically stable viruses of the retrovirus family. This is in contrast to the in vitro error rate found for recombinant FV reverse transcriptase (RT). To investigate the accuracy of FV genome copying in vivo

实验方案

Follow this procedure to rapidly purify single-stranded or double-stranded PCR amplification products (100 bp to 10 kb) from excess primers, nucleotides, DNA polymerase, oil and salts using the GenElute™ PCR Clean-up Kit.

The SeqPlex DNA Amplification Kit for whole genome amplification (WGA) is designed to facilitate next-generation sequencing (NGS) from extremely small quantities or from degraded/highly fragmented DNA

Genomic DNA from soil samples can be easily damaged by nucleases and contaminating debris resulting in low DNA yields. As a result, the researcher’s ability to perform downstream analysis may be compromised. After isolating DNA from the soil sample, the GenomePlex® Whole Genome Amplification Protocol is followed

面向全基因组扩增(WGA)的SeqPlexDNA扩增试剂盒(SEQXE)专用于对极小量或降解/高度片段化的DNA进行下一代测序(NGS)。

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