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綜合目錄PDF 檔下載連結 - 波仕特生物科技股份有限公司

綜合目錄PDF 檔下載連結 - 波仕特生物科技股份有限公司

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RNA Electrophoresis<br />

產 品 目 錄 Product Catalog<br />

生<br />

化<br />

藥<br />

品<br />

核<br />

酸<br />

電<br />

泳<br />

電 泳 需 要 藥 品 與 緩 衝 液 (Agarose, Electrophoresis Buffer and Related Serial Products)<br />

RNA EZ-VISION ® Loading Buffer, 1.5X (Cat. no.: N717)<br />

- 只 需 一 個 步 驟 即 可 完 成 樣 品 的 準 備 和 denature<br />

- 使 用 方 法 為 1.5X loading dye 形 式<br />

例 : sample 5uL + 10 uL RNA EZ-VISION loading buffer, 60 度 10 分<br />

鐘 --> loading gel --> run gel --> UV 觀 察<br />

- 靈 敏 度 : 150 ng RNA<br />

- 後 續 可 做 Northern Blotting<br />

Formaldehyde-Free RNA Gel Kit (Cat. No.: N726)<br />

- 完 全 不 含 Formaldehyde 和 EtBr, 可 以 不 用 在 Hood 內 操 作<br />

- 只 需 一 個 步 驟 即 可 完 成 樣 品 的 準 備 和 denature<br />

- 一 套 kit 可 作 約 30 片 50 mL 的 膠 片<br />

- 內 含 : Formaldehyde-Free RNA Gel Running Buffer 10X, 2X500 mL,<br />

Formaldehyde-Free RNA Gel Solution 10X, 150 mL, Formaldehyde-Free<br />

RNA Gel Loading Buffer 2X, 3X2 mL<br />

- 後 續 可 做 Northern Blotting<br />

Comparison between ethidium bromide and RNA EZ-<br />

Vision®. Total RNA was purified from K562 cells with Ribozol<br />

RNA Extraction Reagent. Samples were denatured at<br />

65°C for 10 minutes in RNA EZ-Vision® loading buffer containing<br />

either 0.003% ethidium bromide or RNA EZ-Vision®<br />

dye. The denatured RNA was loaded onto a 2% formaldehyde<br />

denaturing agarose gel (Agarose I, Code: 0710) and<br />

resolved for 1.5 hours at 5.1 V/cm. Bands were visualized<br />

by UV illumination and image capture was performed with<br />

a Syngene GBox-HR Gel Doc System with a SYBR® Green<br />

filter.<br />

Northern blot analysis of PGK1 mRNA resolved on Formaldehyde- Free RNA Gel.<br />

Gel A: 20 μg of total yeast RNA was applied per lane to an agarose Formaldehyde-Free RNA Gel and resolved at 8V/cm.<br />

Bands were visualized on a UV transilluminator.<br />

Gel B: Bands were transferred to Hybond N+ membrane and probed overnight with a radiolabelled oligonucleotide to<br />

PGK1 mRNA.<br />

Gel C: Membranes were stripped and reprobed overnight with an oligonucleotide to SCR1 RNA loading control. Data<br />

provided by Jeff Coller, Ph.D., Center for RNA Molecular Biology, Case Western Reserve University, Cleveland, Ohio.<br />

Lane 1: Untransformed control Lane 2: High Copy PGK1 vector Lane 3: Low Copy PGK1 vector Lane 4: High Copy PGK1<br />

vector Lane 5: Low Copy PGK1 vector<br />

Comparison of Formaldehyde -Free RNA dye to ethidium bromide<br />

staining. Total RNA was extracted from K562 cells with Ribozol® RNA<br />

Extraction Reagent (N580). Samples were denatured in Formaldehyde-<br />

Free RNA Loading Buffer containing either ethidium bromide or Formaldehyde-Free<br />

RNA dye and incubated for 10 minutes at 65°C. The<br />

samples were applied to a 2% Formaldehyde-Free RNA Agarose Gel<br />

(Agarose I, Code: 0710) and resolved for 1.5 hours at 5.1 V/cm. Image<br />

capture was<br />

24 Protech Technology Enterprise Co., LTD www.bio-protech.com.tw

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