WebNEBioCalculator®. Use this tool for your scientific calculations and conversions for DNA and RNA. Options include conversion of mass to moles, ligation amounts, conversion of OD to concentration, dilution and molarity. Additional features include sgRNA Template Oligo Design and qPCR library quantification. WebDesigning primers for PCR based cloning: The basic PCR primers for molecular cloning consist of: Leader Sequence: Extra base pairs on the 5' end of the primer assist with restriction enzyme digestion (usually 3 …
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WebDec 6, 2024 · The RNA Primer Function. DNA is a double helix consisting of 2 strands: the leading strand and the lagging strand. When a cell is ready to divide, signals are sent to prepare for DNA replication ... WebJun 8, 2024 · Every RNA primer synthesized during replication can be removed and replaced with DNA strands except the RNA primer at the 5′ end of the newly synthesized strand. This small section of RNA can only be removed, not replaced with DNA. ... In the absence of additional cellular processes, nucleases would digest these single-stranded … henry ford health hospital jackson mi
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WebMay 28, 2015 · I found this method: incubate 2 ug RNA with two volumes of denaturing buffer (50 ul formamide, 20 ul formaldehyde, 10 ul 10 X MOPS, and 2 ul ethidium bromide) denature at 70C for 3 minutes and ... WebThe Nucleoside Digestion Mix is an optimized mixture of enzymes that provides a convenient one-step method to generate single nucleosides from DNA or RNA for quantitative analysis by liquid chromatography-mass spectrometry (LC-MS), eliminating the need for sequential multi-step, time-consuming digestion protocols. Convenient one … WebRestriction enzymes can also be used to generate compatible ends on PCR products. In all cases, one or more restriction enzymes are used to digest the DNA resulting in either non-directional or directional insertion into the … henry ford health lakeside