SYBR¢ç Green Nucleic Acid Gel Stain series
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1. DNA Àü±â¿µµ¿: SYBR¢ç Green I Stain°ú EtBrÀÇ °¨µµ ºñ±³

DNA samples (pBR322 Msp I digest) ranging from 1 to 200 ng per lane were separated on a 10 cm x 16 cm x 0.1 cm, 4% vertical MetaPhor Agarose gel prepared in 1X TBE Buffer. The gel war ren for 1 hours at 488V/cm. Following electrophoresis the gel was divided into two, and one half was stained with 1 §¶/§¢ ethidium bromide while the other was stained with SYBR¢ç Green I Stain (1:10,000 dilution of stock). Detection was achieved with standard 300 nm UV transillumination.

2. RNA Àü±â¿µµ¿: SYBR¢ç Green II Stain°ú EtBrÀÇ °¨µµ ºñ±³

Samples of E. coli total RNA were denatured using the following denaturants:
Lane A: Formaldehyde/ Formamide; Lane B: Formamide; Lane C: Glyoxal. Samples were loaded at 2 §¶/lane for the formaldehyde/formamide and formamide only denatured samples, and 4 §¶/lane for the glyoxal denatured samples. Reliant¢â RNA precast Agarose gels were run at 7 V/cm for 40 minutes in 1X MOPS Buffer and post stained with SYBR Green II¢ç gel stain and photo graphed on the Clare Chemical Research, Inc., Dark Reader¢ç Transilluminator.
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- No.1 agarose: SeaKem¢ç LE Agarose
- »ç¿ëÀÌ °£ÆíÇÑ premade buffer: Lonza AccuGene¢ç Buffer ½Ã¸®Áî
- Gradient PCR ±â±â: TaKaRa PCR Thermal Cycler Touch¢ç
- ³»¿­¼º gel maker set¸¦ Æ÷ÇÔÇÑ µðÁöÅÐ Àü±â¿µµ¿ ÀåÄ¡: Mupid¢ç-One