The True MicroChIP-seq kit provides a robust ChIP protocol suitable for the investigation of histone modifications within chromatin from as few as 10 000 cells, including FACS sorted cells. The kit can be used for chromatin preparation for downstream ChIP-qPCR or ChIP-seq analysis. The complete kit contains everything you need for start-to-finish ChIP including all validated buffers and reagents for chromatin shearing, immunoprecipitation and DNA purification for exceptional ChIP-qPCR or ChIP-seq results. In addition, positive control antibodies and negative control PCR primers are included for your convenience and assurance of result sensitivity and specificity.
The True MicroChIP-seq kit offers unique benefits:
For fast ChIP-seq on low input – check out Diagenode’s µChIPmentation for histones.
The True MicroChIP-seq kit, Cat. No. C01010132 is an upgraded version of the kit True MicroChIP, Cat. No. C01010130, with the new validated protocols (e.g. FACS sorted cells) and MicroChIP DiaPure columns included in the kit.
The True MicroChIP-seq kit protocol has been optimized for the use of 10,000 - 100,000 cells per immunoprecipitation reaction. Regarding chromatin immunoprecipitation, three protocol variants have been optimized:
starting with a batch, starting with an individual sample and starting with the FACS-sorted cells.


Figure 1. ChIP efficiency on 10,000 cells. ChIP was performed on human Hela cells using the Diagenode antibodies H3K4me3 (Cat. No. C15410003), H3K27ac (C15410174), H3K9me3 (C15410056) and H3K27me3 (C15410069). Sheared chromatin from 10,000 cells and 0.1 µg (H3K27ac), 0.25 µg (H3K4me3 and H3K27me3) or 0.5 µg (H3K9me3) of the antibody were used per IP. Corresponding amount of IgG was used as control. Quantitative PCR was performed with primers for corresponding positive and negative loci. Figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).

Figure 2. Integrative genomics viewer (IGV) visualization of ChIP-seq experiments using 50.000 of K562 cells. ChIP has been performed accordingly to True MicroChIP protocol followed by the library preparation using MicroPlex Library Preparation Kit (C05010001). The above figure shows the peaks from ChIP-seq experiments using the following antibodies: H3K4me1 (C15410194), H3K9/14ac (C15410200), H3K27ac (C15410196) and H3K36me3 (C15410192).

Figure 3. (A) Integrative genomics viewer (IGV) visualization of ChIP-seq experiments and heatmap 3kb upstream and downstream of the TSS (B) for H3K4me3. ChIP has been performed using 10.000 of FACS-sorted cells (K562) and H3K4me3 antibody (C15410003) accordingly to True MicroChIP protocol followed by the library preparation using MicroPlex Library Preparation Kit (C05010001). Data were compared to ENCODE standards.
The Chromatin EasyShear Kit – High SDS Recommended for the optimizing chromatin shearing.
ChIP-seq grade antibodies for high yields, specificity, and sensitivity.
Check the list of available primer pairs designed for high specificity to specific genomic regions.
For library preparation of immunoprecipitated samples we recommend to use the MicroPlex Library Preparation Kit - validated for library preparation from picogram inputs.
For IP-Star Automation users, check out the automated version of this kit.
Application note: Best Workflow Practices for ChIP-seq Analysis with Small Samples
I am working with the True MicroChIP & Microplex Library Preparation Kits and several histone modification antibodies like H3K27ac, H3K4me3, H3K36me3, and H3K27me3. I got always very good and reproducible results for my ChIP-seq experiments.
Andrea Thiesen, ZMB, Developmental Biology, Prof. Dr. Andrea Vortkamp´s lab, University Duisburg-Essen, Germany
The True MicroChIP-seq kit is compatible with a broad variety of cell lines, tissues and species - some examples are shown below. Other species / cell lines / tissues can be used with this kit.
Cell lines:
Bovine: blastocysts,
Drosophila: embryos, salivary glands
Human: EndoC-ẞH1 cells, HeLa cells, PBMC, urothelial cells
Mouse: adipocytes, B cells, blastocysts, pre-B cells, BMDM cells, chondrocytes, embryonic stem cells, KH2 cells, LSK cells, macrophages, MEP cells, microglia, NK cells, oocytes, pancreatic cells, P19Cl6 cells, RPE cells,
Other cell lines / species: compatible, not tested
Tissues:
Horse: adipose tissue
Mice: intestine tissue
Other tissues: not tested
| True MicroChIP and MicroPlex kits APPLICATION NOTE From minuscule amounts to magnificent results: reliable ChIP-seq data from 10,000 cells with the ... | Download |
| ChIP kit results with True MicroChIP kit POSTER Chromatin immunoprecipitation coupled with high-throughput sequencing (ChIP-seq) has become the g... | Download |
| Application note: Best Workflow Practices for ChIP-seq Analysis with Small Samples APPLICATION NOTE Combined chromatin immunoprecipitation and next-generation sequencing (ChIP-seq) has become the g... | Download |
| Chromatin shearing with the Diagenode One APPLICATION NOTE The Diagenode One is a new affordable solution for Chromatin shearing in ChIP analysis for ... | Download |
| True MicroChIP-seq Kit MANUAL The True MicroChIP-seq kit provides a robust ChIP protocol suitable for the investigation of hist... | Download |
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Intranasal administration of Acinetobacter lwoffii in a murine model ofasthma induces IL-6-mediated protection associated with cecal microbiotachanges. |
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Single-cell-resolved dynamics of chromatin architecture delineate cell
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Autocrine Vitamin D-signaling switches off pro-inflammatory programsof Th1 cells |
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Histone H1 loss drives lymphoma by disrupting 3D chromatin architecture. |
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Trans- and cis-acting effects of Firre on epigenetic features of theinactive X chromosome. |
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Interaction of Sox2 with RNA binding proteins in mouse embryonic stem cells. |
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Whsc1 links pluripotency exit with mesendoderm specification. |
The epigenetic basis for the impaired ability of adult murine retinal pigment epithelium cells to regenerate retinal tissue. |
Spatial confinement downsizes the inflammatory response of macrophages. |
Automethylation-induced conformational switch in Clr4 (Suv39h) maintains epigenetic stability. |
Epigenetic inheritance mediated by coupling of RNAi and histone H3K9 methylation. |
Insulin promoter in human pancreatic β cells contacts diabetes susceptibility loci and regulates genes affecting insulin metabolism. |
Retinoid-Sensitive Epigenetic Regulation of the Hoxb Cluster Maintains Normal Hematopoiesis and Inhibits Leukemogenesis. |
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Histone Deacetylases 1 and 2 Regulate Microglia Function during Development, Homeostasis, and Neurodegeneration in a Context-Dependent Manner. |