Molth ATAC-Seq Kit
Cat No.: MAT241088S, Size: 12 preps
Introduction
The Molth ATAC-seq Kit offers a streamlined and efficient solution for profiling the epigenetic landscape by identifying regions of open chromatin. Utilizing the powerful Assay for Transposase-Accessible Chromatin via Sequencing (ATAC-Seq) method, this kit simplifies the process of tagging and fragmenting DNA in intact nuclei with a hyperactive Tn5 transposase mutant in a single step, known as "tagmentation." Since its introduction, ATAC-Seq has become a preferred method for its speed, simplicity, and sensitivity, making it ideal for a wide range of sample types. The Molth ATAC-seq Kit provides all the necessary reagents to generate Illumina®-compatible sequencing-ready libraries from as little as 10 mg of tissue or 10,000 cells per reaction, enabling researchers to efficiently explore chromatin accessibility and epigenetic regulation.
Product Highlight
01
High Efficiency and Sensitivity
The Molth ATAC-seq Kit is designed to deliver high-efficiency tagmentation, allowing for the generation of sequencing-ready libraries from minimal starting material. With the ability to process as little as 10 mg of tissue or 10,000 cells, this kit ensures reliable and sensitive detection of open chromatin regions across various sample types.
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Comprehensive Reagent Package
This kit includes all necessary reagents for producing 12 or 48 unique Illumina®-compatible ATAC-Seq libraries, streamlining the workflow for researchers. The comprehensive nature of the Molth ATAC-seq Kit ensures consistency and reproducibility, making it an ideal choice for both novice and experienced users in epigenomic studies.
High-quality ATAC-Seq results
The Molth ATAC-seq Kit consistently delivers high-quality ATAC-Seq results, providing clear and distinct peaks that represent regions of open chromatin. For example, browser tracks of well-known genes like GAPDH, Sox2, and Nestin demonstrate sharp peaks at promoter regions, reflecting active chromatin states that are easily distinguishable from background noise. This level of detail enables researchers to confidently identify and quantify accessible chromatin regions, facilitating deeper insights into gene regulation and epigenetic mechanisms.
