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
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 />
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