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True Stranded mRNA Sample Prep LS Protocol Experienced User Card and Lab Tracking Form FOR RESEARCH USE ONLY Date: Illumine Kit Lot #: Description: NOTE Unless familiar with the LS protocol in the
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How to fill out truseq stranded mrna sample:

01
Begin by labeling all the necessary tubes and plates for the truseq stranded mrna sample according to the protocol instructions.
02
Thaw the reagents and primers required for the sample preparation and make sure they are properly mixed before use.
03
Extract total RNA from the cells or tissues using a suitable method such as TRIzol or a column-based purification kit.
04
Assess the RNA quality and quantity using a spectrophotometer or a fluorometer. Ensure that the RNA integrity number (RIN) is above a certain threshold, as specified in the protocol.
05
Dilute the RNA to the desired concentration using nuclease-free water or an appropriate buffer. Mix gently by pipetting up and down.
06
Prepare the master mix by combining the necessary reagents, including the fragmented RNA, first-strand synthesis buffer, dNTPs, random primers, and reverse transcriptase. Mix thoroughly but gently to avoid introducing air bubbles.
07
Add the master mix to each sample tube containing the diluted RNA, ensuring that the reaction is mixed well by pipetting up and down several times.
08
Incubate the samples in a thermal cycler according to the protocol's temperature and duration specifications for reverse transcription.
09
After the reverse transcription step, add second-strand synthesis mix, DNA polymerase, and buffer to each sample tube containing the first-strand cDNA. Mix gently.
10
Incubate the samples in a thermal cycler as indicated in the protocol to generate double-stranded cDNA.
11
Optional: If necessary, perform adenylation and ligation steps to add adapters for sequencing.
12
Purify the cDNA by using a suitable method such as magnetic bead-based purification or column-based purification to remove unincorporated primers, enzymes, and other contaminants.
13
Assess the cDNA quality and quantity using a spectrophotometer or a fluorometer. Ensure that the concentration is within the recommended range for downstream applications.
14
Proceed with downstream applications such as library preparation, sequencing, or gene expression analysis, as required.

Who needs truseq stranded mrna sample?

01
Researchers studying gene expression in different tissues or cell types may require truseq stranded mRNA samples. Examining gene expression patterns can provide insights into various biological processes and disease mechanisms.
02
Scientists investigating transcriptional regulation, alternative splicing, or mRNA isoform analysis could benefit from truseq stranded mRNA samples. These samples can help identify specific RNA isoforms and discern gene regulation mechanisms.
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Pharmaceutical companies developing drugs or therapies might utilize truseq stranded mRNA samples to analyze gene expression changes in response to treatment. This analysis can aid in understanding drug mechanisms, identifying potential biomarkers, or assessing drug efficacy.
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Medical diagnostic laboratories studying gene expression alterations in disease conditions may use truseq stranded mRNA samples to identify potential biomarkers, define disease subtypes, or monitor treatment response.
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TruSeq Stranded mRNA Sample is a type of sample preparation method used in RNA sequencing to analyze the gene expression profile of mRNA molecules.
Researchers and laboratories conducting RNA sequencing experiments are required to file TruSeq Stranded mRNA Sample.
TruSeq Stranded mRNA Sample can be filled out following the specific protocol provided by the manufacturer or the laboratory conducting the RNA sequencing experiment.
The purpose of TruSeq Stranded mRNA Sample is to prepare RNA samples for sequencing in order to analyze gene expression levels and patterns.
TruSeq Stranded mRNA Sample should report details of the mRNA molecules being analyzed, experimental conditions, and any other relevant information for the RNA sequencing experiment.
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