The largest database of trusted experimental protocols

Dna high sensitivity d5000 screentape

Manufactured by Agilent Technologies

The DNA High Sensitivity D5000 ScreenTape is a laboratory instrument designed for the analysis of DNA samples. It provides automated, high-sensitivity electrophoretic separation and detection of DNA fragments ranging from 100 to 5,000 base pairs in length.

Automatically generated - may contain errors

3 protocols using dna high sensitivity d5000 screentape

1

RNA Extraction and Sequencing Workflow

Check if the same lab product or an alternative is used in the 5 most similar protocols
RNA was extracted using the Qiagen RNeasy Plus mini kit (74134) after homogenization by centrifugation in QIAShredder (79656) microcentrifuge tubes. RNA quantity was determined using the Qubit 2.0 Fluorometer (Thermo Fisher Scientific), and the quality was validated using the TapeStation RNA ScreenTape (Agilent). Two hundred nanograms of DNase I–treated total RNA was used to prepare the library for Illumina sequencing using a QuantSeq 3′ mRNA-Seq Library Preparation kit (Lexogen). Library quantity was determined using qPCR (KAPA Biosystem). Overall library size was determined using the Agilent TapeStation and the DNA High Sensitivity D5000 ScreenTape (Agilent). Equimolar amounts of each sample library were pooled, denatured, and sequenced using high-output, single-read, 75-bp-cycle Illumina NextSeq 500 sequencing kits. Next-generation sequencing was done on a NextSeq 500 (Illumina).
+ Open protocol
+ Expand
2

Illumina Sequencing of 3'mRNA Library

Check if the same lab product or an alternative is used in the 5 most similar protocols
100 ng of DNAse treated total RNA was used to prepare library for Illumina sequencing using the Quant-Seq 3’mRNA-Seq Library Preparation Kit (Lexogen, Vienna, Austria). Library quantity was determined using qPCR (KAPA Biosystem, Wilmington, MA), and overall library size was resolved using the Agilent TapeStation and the DNA High Sensitivity D5000 ScreenTape (Agilent, Santa Clara, CA). Equimolar amount of libraries were pooled, denatured and High-Output, single read, 75 base pair Next Generation Sequencing was done on a NextSeq 500 (Illumina, San Diego, CA).
+ Open protocol
+ Expand
3

Illumina RNA-Seq Library Preparation

Check if the same lab product or an alternative is used in the 5 most similar protocols
100 ng of DNAse treated total RNA was used to prepare library for Illumina sequencing using the Quant-Seq 3’mRNA-Seq Library Preparation Kit (Lexogen, Vienna, Austria). Library quantity was determined using qPCR (KAPA Biosystem, Wilmington, MA), and overall library size was resolved using the Agilent TapeStation and the DNA High Sensitivity D5000 ScreenTape (Agilent, Santa Clara, CA). Equimolar amount of libraries were pooled, denatured and High-Output, single read, 75 base pair Next Generation Sequencing was done on a NextSeq 500 (Illumina, San Diego, CA).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!