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一般說明
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.
應用
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[1] and labelling of probes with 32P by random priming.[2]
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]
品質
Function tested in the standard assay.
原則
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.
分析報告
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
其他說明
仅用于生命科学研究。不可用于诊断。
儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
No data available
閃點(°C)
No data available
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