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AB185908

ChIP-Seq High Sensitivity Kit

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(4 Publications)

ab185908 is a complete set of reagents required for carrying out a successful ChIP-Seq starting from mammalian cells or tissues.
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ChIP - ChIP-Seq High Sensitivity Kit (AB185908)
  • ChIP

Supplier Data

ChIP - ChIP-Seq High Sensitivity Kit (AB185908)

Sample results.

A ChIP-sequencing library was prepared using ChIP-Seq High Sensitivity Kit (ab185908) from rat heart chromatin and polyclonal antibodies against H3K4me3, H3(K9/14)ac and, H3K27me3. Sequencing was carried out on an Illumina HiSeq2500. Bioinformatics analysis of ChIP-seq is performed utilizing Bowtie and MACS.

ChIP-sequencing - ChIP-Seq High Sensitivity Kit (AB185908)
  • ChIP-seq

Unknown

ChIP-sequencing - ChIP-Seq High Sensitivity Kit (AB185908)

High sensitive ChIP.

The sheared chromatin isolated from different number of MBD-231 cells was used for ChIP-qPCR analysis of RNA polymerase II enrichment in GAPDH promoters.

Spectrum - ChIP-Seq High Sensitivity Kit (AB185908)
  • Spectrum

Supplier Data

Spectrum - ChIP-Seq High Sensitivity Kit (AB185908)

Size distribution of library fragments.

Ten nanograms of DNA was ChIPed by RNA polymerase II enrichment and used for DNA library preparation.

Key facts

Assay time

7h

Sample types

Tissue, Suspension cells, Adherent cells

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "ChIP-seq": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Product details

ab185908 is a complete set of reagents required for carrying out a successful ChIP-Seq starting from mammalian cells or tissues. The kit is designed to selectively enrich a chromatin fraction containing specific DNA sequences from various species, particularly mammals, and to prepare a ChIP-Seq library for next generation sequencing using Illumina® platforms such as Illumina® Genome Analyzer II, HiSeq and MiSeq systems. The optimized protocol and components of the kit allow capture of low abundance protein/DNA complexes with minimized non-specific background levels and the ability to construct both non-barcoded (singleplexed) and barcoded (multiplexed) ChIP-Seq libraries quickly with reduced bias.

Starting Materials:
Starting materials can include various tissue or cell samples such as culture cells from a flask or plate, fresh and frozen tissues, etc.

Input Amount of Tissue/Cells:

In general, the amount of cells and tissues for each reaction can be 1 x 105 to 1 x 106 and 5 mg to 50 mg, respectively. For optimal preparation, the input amount should be 4 to 5 x 105cells or 20 to 30 mg tissues so that the amount of DNA enriched from the ChIP reaction can range from at least 1 ng to 100 ng.

Illumina® is a registered trademark of Illumina, Inc.

Protein-DNA interaction plays a critical role for cellular functions such as signal transduction, gene transcription, chromosome segregation, DNA replication and recombination, and epigenetic silencing. Identifying the genetic targets of DNA binding proteins and knowing the mechanisms of protein-DNA interaction on a genome-wide scale is important for understanding cellular processes. Chromatin immunoprecipitation (ChIP) followed by next generation sequencing (ChIP-Seq) offers an advantageous tool for studying genome-wide protein-DNA interactions. It allows for detection that a specific protein binds to specific sequences in living cells. In particular, ChIP antibodies targeted against various transcriptional factors (TF) for genome-wide transcription factor binding site analysis by Chip-Seq is in high demand. Such analysis requires that ChIPed DNA contain minimal background for reliably identifying true TF-enriched regions. Currently used ChIP-Seq methods play an important role in identifying genome-wide protein-DNA interaction. The ChIP-Seq High Sensitivity Kit combines microplate-based ultra ChIP and high sensitive DNA library construction technologies.

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
Multi
Appropriate long-term storage conditions
Multi
Storage information
Please refer to protocols

Product protocols

Target data

Publications (4)

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Cancer biology & therapy 25:2299288 PubMed38178596

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WYC-209 inhibited GC malignant progression by down-regulating WNT4 through RARα.

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Pathology, research and practice 238:154076 PubMed36055087

2022

WDR5 drives the development of cervical squamous cell carcinoma by inducing epithelial-mesenchymal transition and cancer-associated fibroblasts formation.

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Fangli Sun,Linmei Mo,Ying Lan,Qiuping Lu,Nengxian Wu,Honglin Song

Scientific reports 11:21500 PubMed34728675

2021

Integrative genome-wide analysis of dopaminergic neuron-specific PARIS expression in Drosophila dissects recognition of multiple PPAR-γ associated gene regulation.

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Volkan Yazar,Sung-Ung Kang,Shinwon Ha,Valina L Dawson,Ted M Dawson

Journal of hepatocellular carcinoma 8:333-348 PubMed33977095

2021

LncRNA-CCDC144NL-AS1 Promotes the Development of Hepatocellular Carcinoma by Inducing WDR5 Expression via Sponging miR-940.

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Yingying Zhang,Hongyu Zhang,Shuhuan Wu
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