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GE25-0500-71

RNAspin Mini 50

greener alternative

Cytiva 25-0500-71

同義詞:

Mini RNA Extraction Kit, RNAspin Mini Kit

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About This Item

分類程式碼代碼:
41105501
NACRES:
NA.52

製造商/商標名

Cytiva 25-0500-71

包裝

pkg of 50 preps

環保替代產品特色

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

容量

100 μg binding capacity

環保替代類別

一般說明

illustra RNAspin Mini RNA Isolation Kit is designed for rapid extraction of high-quality RNA from a wide range of sample types.

illustra RNAspin Mini Isolation Kit can be used to isolate total RNA from cultured cells, tissue, bacteria, or yeast. The isolated RNA is of a high enough quality and quantity (up to 100 μg) for multiple downstream experiments and sensitive enzymatic applications like RT-PCR, primer extension, and RNase protection assays. The RNAspin Mini Kit has been used for the isolation of high-quality total RNA from several types of source material including hard-to-lyse bacterial strains, and applied in downstream experiments such as quantitative reverse transcriptase PCR (QRT-PCR), Northern blot, and microarray experiments. The kit is supplied with a full protocol booklet with a detachable, quick reference protocol card, and all the necessary components including prefilters and DNase I.

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has Inherently Safer Chemistry.
illustra RNAspin Mini RNA Isolation Kit is designed for rapid extraction of high-quality RNA from a wide range of sample types.

illustra RNAspin Mini Isolation Kit can be used to isolate total RNA from cultured cells, tissue, bacteria, or yeast. The isolated RNA is of a high enough quality and quantity (up to 100 μg) for multiple downstream experiments and sensitive enzymatic applications like RT-PCR, primer extension, and RNase protection assays. The RNAspin Mini Kit has been used for the isolation of high-quality total RNA from several types of source material including hard-to-lyse bacterial strains, and applied in downstream experiments such as quantitative reverse transcriptase PCR (QRT-PCR), Northern blot, and microarray experiments. The kit is supplied with a full protocol booklet with a detachable, quick reference protocol card, and all the necessary components including prefilters and DNase I.

應用

Used for the isolation of high-quality total RNA from a wide range of source material including hard-to-lyse bacterial strains. Purified RNA is suitable for use in sensitive downstream applications such as quantitative reverse transcriptase PCR (qRT-PCR), Northern blot and microarray experiments.

特點和優勢

  • High-quality output RNA from diverse sample types.
  • Recovers high-quality total RNA due to the removal of genomic DNA through on-column DNase I treatment.
  • For maximum yield and purity, prefilters are included to reduce lysate viscosity.
  • Results can be obtained with even small amounts of precious sample.
  • Lysis buffer is less susceptible to foaming to ensure valuable RNA sample is not wasted.
  • Simple and convenient format that is suitable for all levels of expertise.

儲存和穩定性

Please be aware this product may be shipped 90 days before the expiration date. For more information on the batch specific expiration date, please contact technical service.

分析報告

To view the Certificate of Analysis for this product, please visit www.cytiva.com.

法律資訊

illustra is a trademark of Cytiva

象形圖

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訊號詞

Warning

儲存類別代碼

3 - Flammable liquids


分析證明 (COA)

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文章

This page shows possible causes and solutions for problems that may occur during RNA preparation.

This article describes the evaluation of Whatman FTA cards from Cytiva for their ability to collect, store, and isolate high-quality RNA from a variety of crude biological samples.

條款

Spectrophotometry can be used to estimate DNA or RNA concentration and to analyze the purity of the preparation.

DNA 和 RNA 樣本的純度和濃度會影響下游應用的結果,例如 PCR。檢視評估和測量核酸純度和濃度的方法。

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

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