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A variety of products designed for use in various PCR procedures. Includes dNTPs, enzymes, assays, arrays, master mixes, reagents, and kits. Products can be used for standard, real-time, direct, high fidelity, hot start, and long range PCR protocols.
GenScript M-MuLV Reverse Transcriptase (M-MLV) is derived from a cloned region of the pol gene of MMLV and isolated from an E coli strain overexpressing this construct To increase cDNA yields and get a higher percentage of longer transcripts the M-MLV Reverse Transcriptase has been modified with reduced RNase H activity and expressed free of exogenous RNases and other nucleases The enzyme can synthesize a complementary cDNA strand initiating from a primer using RNA as template (cDNA synthesis) making it ideal for a wide range of applications
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MMLV-RT is a high-quality reverse transcriptase that synthesizes a complementary DNA (cDNA) strand from mRNA or total RNA. With higher thermostability and reduced RNase H activity, it can be used for synthesis with long messenger RNA templates with high sensitivity and efficiency and is ideal for detecting low-level target genes.
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Lyo-Compatible MMLV-RT is a high-concentration, Moloney Murine Leukemia Virus (MMLV) Reverse Transcriptase (RT) with reduced RNase H activity, which exhibits high sensitivity and efficiency for cDNA synthesis and is suitable for incorporation into wet or lyophilized multiplex RT-PCR assays, allowing high sensitivity detection of low copy number RNA targets.
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Chromatographically purified dimeric form with M.W. of 66 kDa and 51 kDa. A solution in 10 mM potassium phosphate, pH 7.4, 1 mM DTT and 20% glycerol. 9068-38-6
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Our AffinityScript Multiple Temperature Reverse Transcriptase is engineered to be highly thermostable, allowing you to reverse transcribe at your preferred reaction temperature.
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igScript™ Reverse Transcriptase (igScript RT) is a recombinant Moloney Murine Leukemia Virus (MMLV) reverse transcriptase with reduced RNase H activity. It is highly efficient at producing full-length cDNA from long RNA templates. igScript RT is an RNA-directed DNA polymerase which lacks 3´ → 5´ exonuclease activity and is capable of producing cDNA from as little as 50 pg of total RNA for real-time RT-PCR analysis and other applications.Applications: First strand cDNA synthesis for PCR or RT-PCR Gene expression data validation by using RT-PCRBenefits: Recombinant MMLV reverse transcriptase with greatly reduced RNase H activity. Active at temperatures up to 55°C. Highly efficient at producing full-length cDNA from as little as 50 pg of total RNA.Product Includes: igScript™ Reverse Transcriptase 10x igScript™ RT Reaction Buffer
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Our AffinityScript Multiple Temperature Reverse Transcriptase is engineered to be highly thermostable, allowing you to reverse transcribe at your preferred reaction temperature.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Bst 3.0 DNA Polymerase is an in silico designed homologue of Bacillus stearothermophilus DNA Polymerase I, Large Fragment engineered for improved isothermal amplification performance and increased reverse transcription activity. Bst 3.0 DNA Polymerase contains 5' to 3' DNA polymerase activity with either DNA or RNA templates and strong strand displacement activity, but lacks 5' to 3' and 3' to 5' exonuclease activity. Bst 3.0 DNA Polymerase demonstrates robust performance even in high concentrations of amplification inhibitors and features significantly increased reverse transcriptase activity compared to Bst DNA Polymerase.
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MW 225.21 g/mol, Purity >99%. Guanosine derivative, competitively inhibits viral DNA polymerase. High specificity for herpes simplex 1 and 2 (EC₅₀ values are 0.04 and 0.44 μM, respectively) and varicella-zoster viruses (IC₅₀ = 0.22 μM).
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phi29 DNA Polymerase is the replicative polymerase from the Bacillus subtilis phage phi29. This polymerase has exceptional strand displacement and processive synthesis properties. The polymerase has an inherent 3' to 5' proofreading exonuclease activity.
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