Maxima Reverse Transcriptase (200 U/µL)逆转录酶

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Maxima Reverse Transcriptase (200 U/µL)逆转录酶

货号:EP0741,EP0742,EP0743

规格:2000 units,10000 units,4 x 10000 units

价格:642,2141,6725

产品类型:反转录酶

品牌:Thermo Fisher

描述Thermo Scientific Maxima Reverse Transcriptase (RT) was developed throughin vitroevolution of M-MuLV RT. The enzyme possesses an RNA-dependent and DNA-dependent polymerase activity as well as RNaseH activity. The engineered enzyme features dramatically improved thermostability and robustness, and increased synthesis rates compared to wild type M-MuLV RT.Maxima Reverse Transcriptase is capable of reproducible cDNA synthesis from a wide range of input total RNA amounts (from 1pg to 5µg) at elevated temperatures (50 to 65°C), which makes this enzyme an ideal tool for two step RT-qPCR (see supporting data).Due to its high thermostability,Maxima enzyme maintains full activity during the entire reverse transcription reaction, generates the highest yields of cDNA, and is able to synthesize even very long RNA transcripts up to 20kb. The reaction temperature can be increased up to 65°C for efficient transcription of RNA regions with a high secondary structure or to improve specificity using gene specific primers. Due to its increased synthesis rate, the reverse transcriptase reaction can be completed in 15 to 30 min.Highlights• High yields of full-length cDNA up to 20kb• Active up to 65°C• Thermostable—90% active after incubation at 50°C for 60minutes• High sensitivity—reproducible cDNA synthesis from a wide range of total RNA quantities (1pg to 5µg)• Efficient—complete cDNA synthesis in 15to30 minutes• Incorporates modified nucleotidesApplications• Two step RT-PCR• Two step RT-qPCR• First strand cDNA synthesis• Construction of full length cDNA libraries• DNA labeling• Primer extensionAlso available:Maxima First Strand cDNA Synthesis Kit for RT-qPCRHigh thermostability of Maxima Reverse Transcriptase at 50°CReverse transcriptases were incubated in 1X reaction buffer. At the indicated time points (5 to 240minutes), enzyme activity was determined in a standard activity assay.

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