Determine the necessary mass, volume, or concentration for preparing a solution.
BioReagent,Suitable for molecular biology,for DNA and RNA applications BioReagent,for DNA and RNA applications,Suitable for molecular biology 최소한의 기준선 간섭이 필요한 민감한 크로마토그래피 및 분석 워크플로우용.
Room temperature Normal 출고. 정확한 사양은 로트별 COA를 확인하세요.
SDS, COA, 데이터시트, 사양서를 다운로드할 수 있습니다. 로트별 COA는 로트 번호 조회를 통해 확인할 수 있습니다.
크로마토그래피, 유기 합성 및 교차 커플링 반응 분야의 동료 심사 논문 0편에서 인용되었습니다.
Double-stranded DNA Denaturation Buffer, also known as Neutral Transfer Buffer, is primarily composed of 1.5 M NaCl, trace NaOH, and other components, and does not contain sucrose. This reagent is specifically designed for nucleic acid hybridization experiments, particularly suitable for the denaturation of double-stranded DNA in Southern blot experiments.
This product is for research use only. Not for use in diagnostic procedures or other purposes.
Procedure (For Reference Only)
The product can be used directly according to specific experimental requirements. The following are dedicated steps for DNA denaturation and transfer for different membrane types:
1. Transfer to Uncharged Membranes
1.1 DNA Denaturation: Place the gel in 10 volumes of Double-stranded DNA Denaturation Buffer. Incubate at room temperature for 45 minutes with continuous gentle agitation.
1.2 Neutralization Treatment: Briefly rinse the gel with deionized water. Subsequently, submerge the gel in 10 volumes of DNA Neutralization Buffer I. Incubate at room temperature for 30 minutes with gentle agitation. Replace with fresh DNA Neutralization Buffer I and continue incubation for another 15 minutes.
2. Transfer to Charged Nylon Membranes
2.1 Alkaline Denaturation: Place the gel in 5-10 volumes of DNA Alkaline Transfer Buffer. Incubate at room temperature for 15 minutes with continuous gentle agitation.
2.2 Secondary Denaturation: Replace with fresh DNA Alkaline Transfer Buffer and continue incubation for another 20 minutes with gentle agitation.
Notes
If the target DNA fragment length is less than 20 kb, it is recommended to avoid performing depurination reactions to prevent fragment degradation.
If the single-use volume is small, it is recommended to aliquot the reagent appropriately before use to minimize the impact of repeated freezing and thawing on reagent stability.
Use the reagent as soon as possible after opening to avoid reagent inactivation or contamination, which could affect subsequent nucleic acid transfer and hybridization experiment results.
위험성, 취급, 보관 및 규제 준수를 포괄하는 종합 문서.
<<<<<<< HEAD SDS 다운로드 → ======= SDS 다운로드 → >>>>>>> release248-p3Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | 날짜 | 항목 |
|---|---|---|---|
| Certificate of Analysis | Jun 17, 2026 | D1518770 |
당사의 등급 선택 가이드는 카탈로그의 모든 변형 제품에 대해 순도, 안정제 상태 및 용도 적합성을 다룹니다.
Suitable for molecular biology 등급 가이드 보기 → BioReagent 등급 가이드 보기 → for DNA and RNA applications 등급 가이드 보기 →