Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos

11277081001

Roche

Hexanucleotide Mix

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

Sinônimo(s):

nucleotide mix

Faça loginpara ver os preços organizacionais e de contrato


About This Item

Código UNSPSC:
41106300

forma

solution

Nível de qualidade

uso

sufficient for 50 labeling reactions

embalagem

pkg of 100 μL

fabricante/nome comercial

Roche

técnica(s)

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

cor

colorless

solubilidade

water: miscible

temperatura de armazenamento

−20°C

Descrição geral

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.

Especificidade

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.

Aplicação

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

Características e benefícios

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.

Qualidade

Function tested in the Random Primed DNA Labeling Kit.

Princípio

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.

Nota de preparo

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.

Nota de análise

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

Outras notas

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

Código de classe de armazenamento

12 - Non Combustible Liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

No data available

Ponto de fulgor (°C)

No data available


Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

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
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
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
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

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica