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 pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.
Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.
SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.
Cité dans 0 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.
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.
Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.
<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.
Rechercher le COA →Résumé de référence rapide des spécifications et applications du produit.
Voir la fiche technique →Attributs de qualité complets et critères d'acceptation pour cette qualité.
Voir la fiche de spécifications →Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
| Certificate of Analysis | Jun 17, 2026 | D1518770 |
Notre guide de sélection des qualités couvre la pureté, le statut du stabilisant et l'adéquation à l'application pour toutes les variantes de notre catalogue.
Voir le guide des qualités Suitable for molecular biology → Voir le guide des qualités BioReagent → Voir le guide des qualités for DNA and RNA applications →