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一般說明
大分子彻底变性和RNase失活。当裂解物在微量离心管中通过二氧化硅膜旋转时,乙醇的加入会导致RNA结合。 洗涤去除污染物后,在50-100 μL洗脱液中洗脱RNA。 在不到30分钟的时间内可以分离出多达150 μg的总RNA。
如果必须消除所有痕量的DNA污染,建议用DNase I进一步处理。当RNA与GenElute结合柱结合时,可使用柱上DNase I消化装置(DNASE10和DNASE70)进行DNase I消化。或者,为了更严格地去除污染的DNA,可以用扩增级DNase I(AMPD1)处理最终的RNA制剂。
應用
- 大鼠脑的速冻视前区
- 油黑壳菜蛤包含性腺的外套膜组织的中央部分
- 鼠的肝脏
特點和優勢
- 从每个制备物中纯化多达107个细胞或40 mg组织中的总RNA
- 每次制备最多可产生150 μg纯的浓缩总RNA
- 从少至100个细胞中回收RNA
- 简单高效-30分钟内制备12-18次
- 比重力流阴离子交换方法快
- 没有与树脂和磁浆相关的繁琐步骤
- 每个试剂盒的纯化比领先供应商多40%
其他說明
原則
法律資訊
訊號詞
Danger
危險分類
Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Repr. 2 - Skin Corr. 1C - Skin Sens. 1 - STOT RE 2 Oral
標靶器官
Liver,Heart
安全危害
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
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商品
The efficacy of amplification of small quantities of total RNA with the Complete Whole Transcriptome Amplification Kit (WTA2) was examined in this study.
The availability of simple methods for purification of DNA and RNA has greatly facilitated the analysis and characterization of the genome and gene expression. There is a demand to isolate DNA and RNA rapidly and conveniently from a variety of cellular sources, including cells and tissues from mammalian, plant and bacterial cultures.
实验方案
Instructions for purifying viral RNA using GenElute™ Mammalian Total RNA Purification Kits.
Instructions for purifying viral RNA using GenElute™ Mammalian Total RNA Purification Kits.
利用 CRISPR-Cas9 基因组编辑技术创建转基因小鼠
Creating Transgenic Mice using CRISPR-Cas9 Genome Editing
相关内容
Overview of common techniques and downstream applications for extraction and purification of genomic DNA, plasmid DNA, and total RNA from cells, tissue, blood, viruses, and other sample types.
Overview of common techniques and downstream applications for extraction and purification of genomic DNA, plasmid DNA, and total RNA from cells, tissue, blood, viruses, and other sample types.
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