Accéder au contenu
Merck
Toutes les photos(1)

Key Documents

11277081001

Roche

Hexanucleotide Mix

solution, pkg of 100 μL, sufficient for 50 labeling reactions

Synonyme(s) :

nucleotide mix

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme


About This Item

Code UNSPSC :
41106300

Forme

solution

Niveau de qualité

Utilisation

sufficient for 50 labeling reactions

Conditionnement

pkg of 100 μL

Fabricant/nom de marque

Roche

Technique(s)

Northern blotting: suitable
Southern blotting: suitable
cDNA synthesis: suitable (first strand)
hybridization: suitable

Couleur

colorless

Solubilité

water: miscible

Température de stockage

−20°C

Description générale

Convenient oligonucleotide mixture for rapid random-primed labeling of DNA with radioactive, digoxigenin- or biotin-labeled nucleotides. In this method, the complementary DNA strand is synthesized by Klenow polymerase using the 3′-OH termini of the random oligonucleotides as primers.

Spécificité

Heat inactivation: Stop the reaction by adding 2 μl 0.2 M EDTA (pH 8.0) and/or by heating to 65 °C for 10 minutes.

Application

Hexanucleotide Mix is a mixture of hexanucleotides of all possible sequences for random-primed DNA labeling.
Labeled DNA probes with high specific activity are used in a variety of hybridization techniques:
  • Screening of gene libraries
  • Southern and northern blots
  • In situ hybridizations
  • RT-PCR
  • Generation of cDNA libraries
  • Synthesis of first-strand cDNA
  • in the determination of vector titer
  • Second strand synthesis

Caractéristiques et avantages

The product is a 10x concentrated mixture of random hexanucleotides. Statistically, the mix may contain up to 4,096 different hexanucleotides, but these are probably present in differing amounts.

Contents
10x concentrated mixture of hexanucleotides (62.5 A260 units/ml) in reaction buffer [0.5M Tris- HCl, 0.1M MgCl2, 1mM dithioerythritol (DTE), 2mg/ml BSA, pH 7.2 (+20°C)]
Note: The mix is identical to that supplied in vial 5 of the DIG DNA Labeling and Detection Kit and of the DIG DNA Labeling Kit and in vial 6 of the Random Primed DNA Labeling Kit.

Qualité

Function tested in the Random Primed DNA Labeling Kit.

Principe

The "random primed" DNA labeling method developed by Feinberg and Vogelstein is based on the hybridization of a mixture of all possible hexanucleotides to the DNA to be labeled. All sequence combinations are represented in the hexanucleotide primer mixture, which leads to binding of primer to the template DNA in a statistical manner. Thus, an equal degree of labeling along the entire length of the template DNA is guaranteed. The complementary strand is synthesized from the 3′-OH termini of the random hexanucleotide primer using Klenow enzyme, labeling grade. Modified deoxyribonucleoside triphosphates ([32P], [35S],[3H], or [125I] digoxigenin- or biotin-labeled) present in the reaction are incorporated into the newly synthesized complementary DNA strand.

Notes préparatoires

Assay Time
Standard labeling (radioactive): 50 minutes
Labeling assay with digoxigenin-11-dUTP: 80 minutes

Sample Materials
  • DNA fragments
  • Linearized plasmid DNA
  • λDNA
Note: The length of the DNA fragments to be labeled does not influence the reaction. DNA fragments of 100bp length are labeled equally well as linearized plasmid- or λ-DNA. The input DNA serves solely as template for the synthesis of labeled DNA, and is not degraded during the reaction, making it possible to label minimal amounts of DNA (10ng) using this method.

Synthesis: All 4 bases are used to synthesize this random hexanucleotide mix. In the initial reaction, starter nucleotides are linked to a solid phase support. In subsequent coupling reactions, equimolar amounts of the 4 dNTPs are linked to the starter nucleotides until hexamers are generated. The hexamers are then released from the solid phase support.
Post-synthesis: The oligonucleotides are HPLC purified, desalted, and 5′-phosphorylated.

Remarque sur l'analyse

Absorption: 62.5 A260 units correspond to 2.5 mg/ml of hexanucleotides.

Autres remarques

For life science research only. Not for use in diagnostic procedures.

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

No data available

Point d'éclair (°C)

No data available


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Roumen Voutev et al.
Developmental biology, 298(1), 45-58 (2006-08-01)
Ribosome biogenesis is a cell-essential process that influences cell growth, proliferation, and differentiation. How ribosome biogenesis impacts development, however, is poorly understood. Here, we establish a link between ribosome biogenesis and gonadogenesis in Caenorhabditis elegans that affects germline proliferation and
Andrew L Goodman et al.
Nature protocols, 6(12), 1969-1980 (2011-11-19)
Insertion sequencing (INSeq) is a method for determining the insertion site and relative abundance of large numbers of transposon mutants in a mixed population of isogenic mutants of a sequenced microbial species. INSeq is based on a modified mariner transposon
Elise Alspach et al.
Bio-protocol, 5(10) (2015-05-20)
Immunoprecipitation and subsequent isolation of nucleic acids allows for the investigation of protein:nucleic acid interactions. RNA-binding protein immunoprecipitation (RIP) is used for the analysis of protein interactions with mRNA. Combining RIP with quantitative real-time PCR (qRT-PCR) further enhances the RIP
Chen Ling et al.
Journal of visualized experiments : JoVE, (49)(49), doi:10-doi:10 (2011-03-30)
Recombinant vectors based on a non-pathogenic human parvovirus, the adeno-associated virus 2 (AAV2) have been developed, and are currently in use in a number of gene therapy clinical trials. More recently, a number of additional AAV serotypes have also been
Dilip Kumar et al.
Journal of immunology (Baltimore, Md. : 1950), 182(2), 1011-1020 (2009-01-07)
The MAPKs ERK, JNK, and p38 control diverse aspects of the immune response, including regulation of cytotoxin biology in NK cells and CTL. The chemokine CCL5 is coreleased with the cytotoxins, perforin, the granzymes, and granulysin, during the lethal hit

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique