Web• Using smaller amounts of ready reaction mix – ABI still recommend the use of 8ul of the mix in a 20ul total volume – As the mix is relative expense most people use less than the 8ul –4ul and even 2ul are commonly used. – However if you want to use even less reagent, it Web• 2 × 20-ml tubes of BigDye™ Terminator v3.1 Ready Reaction Mix • 2 tubes M13 (-21) Primer • 2 tubes pGEM Control DNA • 2 × 28-ml tubes of 5X Sequencing Buffer (may be stored at 4°C) Store kit at -15°C to -25°C and avoid repeated freeze-thaw cycles. Format: 96- or 384-well Plate, 8-well Strips, 12-well Strips: For Use With ...
Taq PCR Reaction Mix - Sigma-Aldrich
WebReady-mix format reduces setup time. Reproducibility - Reduces the risk of contamination from multiple pipet steps and provides consistent performance across both reactions and time. High Specificity & Yield - JumpStart Taq DNA polymerase, an antibody inactivated hot-start enzyme, is designed to minimize non-specific amplification while ... Web“Ready-To-Load Sanger Sequencing (BigDye reactions performed by customer)” ... Appendix 1: BigDye Reaction The following is the master mix and protocol that the Genomics Core at Cornell University follows for Sanger sequencing premixed template and primer sample. Mix for each sample in 96 or 384 well PCR plate: fmsweb aos
Big Dye sequencing protocol - University of California …
WebContents & Storage. Each kit contains 2 × 20-ml tubes of BigDye™ Terminator v1.1 Ready Reaction Mix, 2 tubes of M13 (-21) Primer, 2 … WebReady Reaction Mix and are ready to use. These reagents are suitable for performing fluorescence-based cycle sequencing reactions on single-stranded or double-stranded DNA templates, on polymerase chain reaction (PCR) fragments, and on large templates, e.g., BAC clones. The dNTP mix includes dITP in place of dGTP to minimize band Webvolumes for a single 20 μL 1-step RT-qPCR reaction. For multiple reactions, prepare a master mix of components common to all reactions to minimize pipetting error, then dispense the appropriate volumes into the qPCR plate before adding the template. Steps 1. Thaw reagents: Thaw, mix, and briefly centrifuge each component before use. 2. green silk throw