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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.
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:
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, 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.
特異性
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.
アプリケーション
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
High Prime has been used to label the probes by random hexamer labelling and labelling of probes with 32P by random priming.
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 and labelling of probes with 32P by random priming.
品質
Function tested in the standard assay.
原理
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.
アナリシスノート
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
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
その他情報
For life science research only. Not for use in diagnostic procedures.
保管分類コード
12 - Non Combustible Liquids
WGK
WGK 1
引火点(°F)
No data available
引火点(℃)
No data available
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
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