TBE Buffer (Tris-borate-EDTA) (10X)
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TBE Buffer (Tris-borate-EDTA) (10X)
Thermo Scientific™

TBE Buffer (Tris-borate-EDTA) (10X)

Thermo Scientific 10X TBE Buffer (Tris-borate-EDTA) is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE자세히 알아보기
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카탈로그 번호수량
B521 L
카탈로그 번호 B52
제품 가격(KRW)
75,000
キャンペーン価格
Ends: 31-Dec-2025
83,000
할인액 8,000 (10%)
Each
카트에 추가하기
수량:
1 L
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
75,000
キャンペーン価格
Ends: 31-Dec-2025
83,000
할인액 8,000 (10%)
Each
카트에 추가하기
Thermo Scientific 10X TBE Buffer (Tris-borate-EDTA) is the most commonly used buffer for DNA and RNA polyacrylamide gel electrophoresis. TBE is used with non-denaturing or denaturing (7 M urea) gels. It is also routinely used for DNA automated sequencing gel. TBE can also be used for agarose gels, but is not recommended for preparative gels for recovery of nucleic acids. Since borate in TBE buffer is a strong inhibitor for many enzymes, TAE buffer (Tris Acetate-EDTA buffer, 10X powder, sc-296647) is recommended when looking at enzymatic applications for the DNA sample.

Applications

• Electrophoresis of nucleic acids in agarose and polyacrylamide gels
• Used both as a running buffer and as a gel preparation buffer
• Filtered through a 0.22 μm membrane
• Recommended for electrophoresis of RNA and DNA fragments smaller than 1500 bp

Note
Double-stranded linear nucleic acid molecules migrate about 10% slower in TBE buffer than in TAE buffer.
For Research Use Only. Not for use in diagnostic procedures.
사양
제품 유형TBE Buffer
수량1 L
농도10X
Unit SizeEach

자주 묻는 질문(FAQ)

For the purpose of recovering and solubilizing nucleic acids in alcohol, can TAE running buffer be used instead of TBE running buffer when running a pre-cast TBE gel?

A TAE running buffer used in conjunction with a TBE gel would create high current and may lead to gel hydrolysis. Also, the acetate ion in TAE migrates faster than the borate ion in TBE buffer, and can create fuzzy bands. It is possible to try soaking the TBE gel (run in TBE buffer) in the TAE buffer following the run and then eluting from that. Since nucleic acids diffuse out of the gel relatively slowly, this may work.

Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.