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Merck
모든 사진(2)

주요 문서

11585592001

Roche

High Prime

solution, sufficient for 50 labeling reactions, pkg of 200 μL

동의어(들):

high prime, labeling mix

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200 μL
₩620,470

₩620,470


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200 μL
₩620,470

About This Item

UNSPSC 코드:
41105500

₩620,470


구입 가능 여부는 고객센터에 문의하십시오.

양식

solution

Quality Level

사용

sufficient for 50 labeling reactions

포장

pkg of 200 μL

제조업체/상표

Roche

저장 온도

−20°C

일반 설명

Contents:
5x concentrated random primer mix: 1 U/μl Klenow polymerase, labeling grade, 0.125 mM dATP, 0.125 mM dGTP, 0.125 mM dTTP in 50% (v/v) glycerol.
Enzyme and nucleotide mixture for rapid random-primed labeling of DNA with [32P], [35S], or [3H] dCTP. In this method, the complementary DNA strand of denatured DNA is synthesized by Klenow polymerase using the 3′-OH termini of the random oligonucleotides as primers.
High Prime is used for rapid random-primed labeling of DNA with [32P], [35S], or [3H]dCTP to a guaranteed specific activity of >2 x 109 dpm/μg. Incubation time is only 10 minutes at +37°C.
High Prime guarantees efficient labeling of:
  • DNA amounts ranging from 10 ng to 3 μg in a standard reaction
  • DNA of different lengths ranging from small restriction fragments to l or cosmid DNA
  • DNA, supercoiled or linearized
  • DNA in low melting-point agarose.
High Prime-labeled DNA probes are suitable for single-copy gene detection in mammalian DNA in Southern, northern, and dot blots, as well as in colony- or plaque hybridization.
High Prime, a novel labeling mixture, contains optimal concentrations of nucleotides and primers in a highly efficient reaction mix with Klenow enzyme. This convenient "all-in-one" principle of High Prime reduces pipetting steps to a minimum, and increases accuracy and reproducibility of labeling reactions.

특이성

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.

애플리케이션

For the labelling of DNA with radioactive dCTP using random oligonucleotides as primers.
High Prime-labelled probes are used in a variety of hybridization techniques: Southern blots
  • Northern blots
  • Dot/slot blots
  • Screening of gene libraries
  • In situ hybridizations

High Prime has been used to label the probes by random hexamer labelling[1] and labelling of probes with 32P by random priming.[2]

품질

Function tested in the standard assay.

원리

Labeled probes are generated with High Prime according to the random-primed labeling technique. High Prime is a specifically developed reaction mixture containing random oligonucleotides, Klenow polymerase, labeling grade, dATP, dGTP, and dTTP in an optimized reaction buffer concentrate in 50% glycerol for rapid and efficient labeling of DNA with [32P]-, [35S]-, or [3H]-labeled dCTP.

분석 메모

Specific Activity: The standard assay routinely yields a specific activity of 2 x 109 dpm/μg, using different substrate DNAs after 10 minutes of incubation.
Assay Time: 30 minutes
Sample Materials
  • DNA fragments of at least 100 bp
  • Linearized plasmid, cosmid or λDNA
  • Supercoiled DNA
  • Or minimal amounts of DNA (10 ng), e.g., DNA restriction fragments isolated from gels or in molten agarose
Note: The length of the DNA to be labeled does not influence the reaction. Maximal incorporation may require a prolonged incubation period of 30 to 60 minutes.

기타 정보

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

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

No data available

Flash Point (°C)

No data available


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