The HiPure Fruit RNA Mini Kit provides fast purification of high-quality RNA from fruits, 細胞, 組織, and yeast using silica-membrane spin columns with a binding capacity of 100µg RNA. There is no need for phenol/chloroform extractions and time-consuming steps such as CsCl gradient ultracentrifugation or precipitation with isopropanol or LiCl. RNA purified using the RaPure Total RNA Purification System can be used for applications such as RT-聚合酶鍊式反應, 北方印跡, poly A+ RNA(信使RNA) purification, nuclease protection and in vitro translation.
細節
規格
特徵 | 規格 |
主要功能 | Isolation total RNA from <150 mg fruit or seed using chloroform and Plantzol reagent |
應用領域 | 逆轉錄聚合酶連鎖反應, 定量PCR, 北方雜交, Poly A purification, nucleic acid protection and in vitro translation translation |
純化方法 | 小型的 旋轉柱 |
淨化技術 | 二氧化矽技術, DNA filtration technology |
工藝方法 | 手動的 (離心或真空) |
樣品類型 | Simple plant, petal, peel, seed |
樣品量 | 50-150毫克 |
洗脫體積 | ≥300μl |
每次運行時間 | ≤15 minutes(1-24 samples) |
每根柱的載液量 | 800微升 |
柱結合率 | 100微克 |
原則
The Kit isolates total RNA from up to 150mg plant tissue. A short workflow enables RNA isolation with genomic DNA removal in less than 15 分分鐘. Samples are first lysed and homogenized. The lysate is passed through a DNA Mini column, ethanol is added to the flow-through, and the sample is applied to an RNA column. RNA binds to the membrane and contaminants are washed away. High-quality RNA is eluted in as little as 300µl water using the Kit.
優點
- 高效 DNA 去除 – 一步 RNA萃取 可有效去除基因組DNA
- 高品質 – 一步RNA萃取試劑結合矽膠柱可獲得最高濃度
- 快速地 – 可以提取多個樣本 15 分鐘柱法
- Wide range – 樣本包括動物, 植物, 細菌, 細胞, ETC
- 高輸出 – large sample amount, and the yield can be up to 200μg
套件內容
內容 | R401402 | D401403 |
淨化時間 | 50 準備工作 | 250 準備工作 |
HiPure RNA 迷你柱 | 50 | 250 |
2毫升收集管 | 50 | 250 |
PlantZol Reagent | 60 毫升 | 200 毫升 |
Buffer GXP | 30 毫升 | 150 毫升 |
緩衝器RW1 | 50 毫升 | 200 毫升 |
緩衝器 RW2* | 20 毫升 | 2 X 50 毫升 |
無核糖核酸酶水 | 10 毫升 | 30 毫升 |
儲存和穩定性
The Kit can be stored dry at room temperature (15–25°C) 並且至少穩定 18 在這些條件下幾個月. During shipment, crystals or precipitation may form in the Buffer RLC/PRC1. Dissolve by warming buffer to 37°C.
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