跳转至内容
Merck
CN
所有图片(3)

文件

安全信息

XNAP

Sigma-Aldrich

REDExtract-N-Amp™植物PCR试剂盒

sufficient for 100 extractions, sufficient for 100 amplifications

登录查看公司和协议定价
所有图片(3)
别名:
Plant direct PCR kit, Plant direct PCR kit with loading dye
UNSPSC代码:
12352200
NACRES:
NA.55

用途

sufficient for 100 amplifications
 sufficient for 100 extractions
 sufficient for 100 reactions

质量水平

200

特点

dNTPs included
hotstart

技术

PCR: suitable

颜色

red

运输

wet ice

储存温度

−20°C

正在寻找类似产品? 访问 产品对比指南

相关类别

一般描述

The REDExtract-N-Amp™植物PCR试剂盒能够通过直接PCR（聚合酶链反应）快速检测植物病原体。这些试剂盒提供了从植物叶片快速提取基因组DNA以及通过直接PCR扩增靶标所需的所有试剂。REDExtract-N-Amp PCR ReadyMix™含有染料，可作为追踪染料并方便地将PCR反应产物上样到琼脂糖凝胶上进行分析。

应用

REDExtract-N-Amp™ Plant PCR试剂盒已用于：
  • 从菌丝草坪和树叶中提取基因组DNA
  • 筛选推定转基因马铃薯植株的叶片组织
  • 进行聚合酶链式反应（PCR）
  • 从大麻种子和干果体鳃中分离DNA

特点和优势

  • 一步提取PCR所需的植物基因组DNA，只需不到15分钟
  • 无需冷冻、机械破碎、有机萃取、柱纯化或液氮冷冻植物组织、机械破碎、有机提取、柱纯化或沉淀
  • 专门配制的PCR ReadyMix，与提取液配套使用
  • 热启动抗体支持高特异性PCR扩增基因组DNA
  • REDExtract-N-Amp™不需要凝胶分析所需的装载缓冲液或跟踪染料
  • 符合高通量植物基因分析要求
  • 提取物稳定：在4 °C环境下稳定至少6个月

组分

试剂盒包括稀释溶液、提取溶液和Extract-N-Amp PCR Reaction Mix。

其他说明

有关其他信息，请参阅www.sigma-aldrich.com/extract-n-amp。

法律信息

购买本产品包括豁免根据产品说明书中所规定的专利提起的诉讼，仅可将所购买的量用于购买者自己的内部研究。′其他专利权（例如5′核酸酶工艺的专利权）不得明示、暗示或禁止反言。 有关购买许可的更多信息，可联系许可总监（Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA）获取。
根据美国专利号 5,338,671和5,587,287以及其他国家的相应专利获得抗体体外研究许可。

本产品的使用受到如下一项或多项美国专利及其对应的境外专利声明保护： 5,789,224、5,618,711、6,127,155和美国境外的声明，对应于过期的美国专利号5,079,352。 购买本产品，即相当于依照境外的专利声明获得了一份受限制、不可转让的使用许可，即将此等数量的产品用于购买者′内部的研究用途。未通过明示、暗示或禁止反言形式授予购买者任何专利主张下的权利、执行任何专利方法的权利或开展任何形式的商业服务的权利，包括但不限于出于经济利益或其他商业考虑报告购买者′的活动结果。本品仅供研究使用。如需用于Roche专利许可的诊断用途，需另外征得Roche许可。有关购买许可的更多信息，可联系许可总监（Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA）获取。
REDExtract-N-Amp is a trademark of Sigma-Aldrich Co. LLC
ReadyMix is a trademark of Sigma-Aldrich Co. LLC

相关产品

产品编号
说明
价格

XNAPE

REDExtract-N-Amp™植物PCR试剂盒, sufficient for 100 extractions, sufficient for 500 amplifications

XNAP2

Extract-N-Amp™植物PCR试剂盒, sufficient for 100 extractions, sufficient for 100 amplifications

XNAR

Extract-N-Amp™植物PCR试剂盒, sufficient for 1000 extractions, sufficient for 1000 amplifications

XNAPR

REDExtract-N-Amp™植物PCR试剂盒, sufficient for 1000 extractions, sufficient for 1000 amplifications

XNAPS

REDExtract-N-Amp™植物PCR试剂盒, sufficient for 10 extractions, sufficient for 10 amplifications

R4775

REDExtract-N-Amp™ PCR ReadyMix™, Ready-to-use 2X PCR Master Mix with Loading Dye

E3004

提取-N-Amp™ PCR ReadyMix™, Amplifications to support Extract-N-Amp Plant and Extract-N-Amp Tissue

E8155

Extract-N-Amp™ PCR Diluent, colorless, storage temp.:2-8°C

D5688

Dilution Solution, Extract-N-Amp Plant Dilution Solution

XNAPG

SYBR® Green Extract-N-Amp™植物PCR试剂盒, sufficient for 100 preparations

S4320

SYBR® Green Extract-N-Amp™ PCR ReadyMix™, Amplifications to support Extract-N-Amp Plant and Extract-N-Amp Tissue

E0781

Extract-N-Amp™ PCR ReadyMix™ with qPCR Reference dye, 125 mL sufficient for 10000 amplifications, hotstart, dNTPs included

象形图

Exclamation markEnvironment
GHS07,GHS09

警示用语：

Warning

危险分类

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品
含少量动物源组分生物产品

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ （Lot或Batch）字后找到。

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Rebeca Cobos et al.
Applied and environmental microbiology, 81(18), 6474-6483 (2015-07-15)
Grapevine trunk fungal pathogens, such as Diplodia seriata and Phaeomoniella chlamydospora, can infect plants through pruning wounds. They cause grapevine trunk diseases and are involved in grapevine decline. Accordingly, the protection of pruning wounds is crucial for the management of
Yolanda Arana-Gabriel et al.
Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 49(3), 632-640 (2018-02-28)
The present study conducted a genetic characterization and determined growth rate and biomass production in solid and liquid media, using strains obtained from wild edible sporomes of Lyophyllum that grow in high mountains. Vegetative isolation was used to obtain a
Samuel J Harrison et al.
Plant methods, 2, 19-19 (2006-11-08)
The floral dip method of transformation by immersion of inflorescences in a suspension of Agrobacterium is the method of choice for Arabidopsis transformation. The presence of a marker, usually antibiotic- or herbicide-resistance, allows identification of transformed seedlings from untransformed seedlings.
Giuseppe Forlani et al.
Forensic science international. Genetics, 52, 102464-102464 (2021-01-19)
The availability of molecular markers able to distinguish drug-type from fiber-type Cannabis sativa cultivars would allow fast and cheap analysis of any plant specimen, including seeds and leaves. Several approaches to this issue have been described, mainly using polymorphisms in
Siobhan M Brady et al.
Molecular systems biology, 7, 459-459 (2011-01-20)
Tightly controlled gene expression is a hallmark of multicellular development and is accomplished by transcription factors (TFs) and microRNAs (miRNAs). Although many studies have focused on identifying downstream targets of these molecules, less is known about the factors that regulate
查看所有相关文献

商品

Extract-N-Amp™ Plant PCR Kits

Extract-N-Amp kits extract and amplify genomic DNA, optimized for plant tissue without inhibition concerns.

Extract-N-Amp™ Product Guide

Extract-N-Amp™ PCR kits are the world’s first integrated extraction and amplification process for rapid blood, tissue or plant assays.

Genomic DNA Purification and Assessment

Simple DNA/RNA purification methods aid genome analysis from various sources, enhancing research efficiency.

基因组DNA样品纯化和质量评估

简单的DNA和RNA纯法方法大幅推动了基因组和基因表达的分析和鉴定。人们需要快速、方便地从多种细胞来源分离DNA和RNA，包括哺乳动物、植物和细菌培养物来源的细胞和组织。

相关内容

Modern Plant Breeding

Explore technology and reagent portfolios for plant breeding workflows, accelerating the development of new crop varieties.

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门