Zymo-Seq ATAC Library Kit provides a simple and streamlined workflow for Assay for Transposase Accessible Chromatin with high throughput Sequencing (ATAC-Seq) library preparation from mammalian cell and tissue input. This all-inclusive kit features an easy to follow protocol capable of preparing ATAC-Seq libraries from as little as 50,000 cells in as little as 4 hours with minimal hands on time.
Initial cell lysis is gentle, ensuring that while the important nuclei are spun out of the lysed cell and collected, the contaminating mitochondrial DNA stays within the cell and is discarded. Next, the transposase, preloaded with Illumina adaptors, simultaneously fragments and tags (tagments) open chromatin regions in one rapid reaction. Finally, the tagmented DNA is indexed and amplified via PCR with UDI Tag Primer Set, generating high quality libraries that are ready to be sequenced on any Illumina instrument.
Ready to Use: Preassembled buffers allow for lightning-fast library preparation in as little as 4 hours without compromising quality.
Improved Performance: Prepare libraries with 7x less mitochondrial contamination, saving reads and increasing sequencing depth.
Outstanding Consistency: Produce highly correlated replicates from both fresh and frozen samples.
DESCRIPTION
Zymo-Seq ATAC Library Kit provides a simple and streamlined workflow for Assay for Transposase Accessible Chromatin with high throughput Sequencing (ATAC-Seq) library preparation from mammalian cell and tissue input. This all-inclusive kit features an easy to follow protocol capable of preparing ATAC-Seq libraries from as little as 50,000 cells in as little as 4 hours with minimal hands on time.
Initial cell lysis is gentle, ensuring that while the important nuclei are spun out of the lysed cell and collected, the contaminating mitochondrial DNA stays within the cell and is discarded. Next, the transposase, preloaded with Illumina adaptors, simultaneously fragments and tags (tagments) open chromatin regions in one rapid reaction. Finally, the tagmented DNA is indexed and amplified via PCR with UDI Tag Primer Set, generating high quality libraries that are ready to be sequenced on any Illumina instrument.
TECHNICAL SPECIFICATIONS
DNA Input
For optimal results, use 50,000 cells per technical replicate. Cells should present viability (measure of the proportion of live cells within a population) >80%. Recommend using cell counter to measure viability accurately.
Equipment Required
Microcentrifuge, Biosafety cabinet, Cell counter, water bath, thermocycler, and thermoshaker with capacity to heat to 37°C and shake at 1000 rpm (We recommend USA Scientific Mixer HC™ with a thermo block that can fit 1.5 mL tubes and 2 mL Low Binding tubes).
Library Storage
Libraries eluted in DNA Elution Buffer may be stored at 4°C overnight or at -20°C for long term storage.
Processing Time
~ 4 hours
Reagents Not Provided
Trypan blue, PBS, DNase I, cell media, trypsin, FBS, and DMSO.
Sequencing Platform Compatibility
Libraries are compatible with Illumina sequencing platforms (HiSeq™, NextSeq™, NovaSeq™).
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Price
4.985,00 RON (preturile sunt fara TVA)
Description
HIGHLIGHTS
Ready to Use: Preassembled buffers allow for lightning-fast library preparation in as little as 4 hours without compromising quality.
Improved Performance: Prepare libraries with 7x less mitochondrial contamination, saving reads and increasing sequencing depth.
Outstanding Consistency: Produce highly correlated replicates from both fresh and frozen samples.
DESCRIPTION
Zymo-Seq ATAC Library Kit provides a simple and streamlined workflow for Assay for Transposase Accessible Chromatin with high throughput Sequencing (ATAC-Seq) library preparation from mammalian cell and tissue input. This all-inclusive kit features an easy to follow protocol capable of preparing ATAC-Seq libraries from as little as 50,000 cells in as little as 4 hours with minimal hands on time.
Initial cell lysis is gentle, ensuring that while the important nuclei are spun out of the lysed cell and collected, the contaminating mitochondrial DNA stays within the cell and is discarded. Next, the transposase, preloaded with Illumina adaptors, simultaneously fragments and tags (tagments) open chromatin regions in one rapid reaction. Finally, the tagmented DNA is indexed and amplified via PCR with UDI Tag Primer Set, generating high quality libraries that are ready to be sequenced on any Illumina instrument.
TECHNICAL SPECIFICATIONS
DNA Input
For optimal results, use 50,000 cells per technical replicate. Cells should present viability (measure of the proportion of live cells within a population) >80%. Recommend using cell counter to measure viability accurately.
Equipment Required
Microcentrifuge, Biosafety cabinet, Cell counter, water bath, thermocycler, and thermoshaker with capacity to heat to 37°C and shake at 1000 rpm (We recommend USA Scientific Mixer HC™ with a thermo block that can fit 1.5 mL tubes and 2 mL Low Binding tubes).
Library Storage
Libraries eluted in DNA Elution Buffer may be stored at 4°C overnight or at -20°C for long term storage.
Processing Time
~ 4 hours
Reagents Not Provided
Trypan blue, PBS, DNase I, cell media, trypsin, FBS, and DMSO.
Sequencing Platform Compatibility
Libraries are compatible with Illumina sequencing platforms (HiSeq™, NextSeq™, NovaSeq™).