Chromatin Immunoprecipitation-on-chip (ChIP-chip)

ChIP-chip Icon

Chromatin immunoprecipitation-on-chip (ChIP-chip) is a powerful tool to map target protein DNA binding sites across entire genomes or within biologically important regions such as promoters. This method is used to map chromatin structure and DNA binding sites of transcription factors and polymerases. Roche NimbleGen offers several types of ChIP-chip arrays for a variety of organisms to meet your specific research needs:

  • Whole-Genome Designs cover all unique genomic regions in single arrays or multi-array sets and offer unbiased, comprehensive genome coverage for the most complete data sets possible.
  • Promoter Designs cover important regulatory regions. Deluxe Promoter arrays offer extensive, single-slide coverage of those regions including gene and miRNA promoters, and CpG islands, while promoter arrays cover only gene promoters.
  • Targeted Designs focus on ENCODE regions (up to 30 Mb), promoters of non-coding RNAs or the HOX clusters.
  • Custom Designs allow researchers to specify their regions of interest for a fine-tiling approach or design their own targeted probes for a tailored array solution.

Advantages

Comprehensive Set of Array Designs Cover All Your Needs

Roche NimbleGen offers whole genome, promoter, and custom array designs, allowing you to choose the design that meets your research requirements. Our whole-genome ChIP-chip designs interrogate the non-repetitive regions of human, mouse, Arabidopsis, rat, dog, chicken, worm, fly, yeast, and E. coli genomes at intervals of 100bp or less for unbiased discovery of promoter/enhancer elements, transcription factor binding, histone modification/replacement, and DNase-I hypersensitivity. NimbleGen human and mouse promoter array designs, based on the latest public genome builds, tile across the promoters of known gene transcripts. You can also order an array design utilized by the ENCODE consortium or tailor an array specific to your experimental design.

High-Resolution, High-Throughput ChIP-chip Analysis

NimbleGen ChIP-chip microarrays are available in four formats: 2.1M (2.1 million probes on a single glass slide), 3x720K (3 identical arrays per glass slide with 720,000 probes per array), 385K (385,000 probes on a single glass slide), and 4x72K (4 identical arrays per glass slide with 72,000 probes per array). This high density provides for high-resolution tiling of your research genome and precise mapping of protein binding sites. With 2.1M arrays, the entire non-repetitive human and mouse genomes can be surveyed at 100bp intervals, each with a set of 10 arrays. Now with 3x720K and 4x72K arrays, you can increase sample throughput and lower cost per sample for targeted ChIP-chip analysis.

High Sensitivity and Specificity Provide Unparalleled Results

Roche NimbleGen's proprietary, light-mediated synthesis process produces high-density microarrays of long oligonucleotide probes (50-75mer). These long oligo arrays, when used in combination with high-stringency hybridization protocols, produce results of unparalleled sensitivity and specificity. In addition, because Roche NimbleGen performs ChIP-chip experiments in a two-color protocol, where control and test samples are co-hybridized to the same array, inter-array variation is eliminated. As a result, NimbleGen ChIP-chip service can readily detect enrichment as low as two-fold of the target binding site in a ChIP sample, which can be extremely challenging for other array platforms to match.

Figure A

Figure A

Figure A. Identification of RNA Polymerase II Binding Sites in MCF7 cells using a HG18 RefSeq Promoter array. NimbleGen's graphical output enables you to visualize protein/DNA interactions.

Easy-to-use Graphical View of Data Aids Discovery

Roche NimbleGen SignalMap software enables you to visually interpret your data and perform peak finding. SignalMap’s graphic representation of your data aids the discovery of promoter/enhancer elements, transcription factor binding, and histone modification/replacement, and DNase-I hypersensitivity. A free, 30-day demo version of SignalMap software is available for download.

Most Up-to-date Genome Builds Ensure Most Accurate Results

NimbleGen ChIP-chip designs are based on the latest genome assemblies and sequence annotations to ensure comprehensive and accurate representation of the genome. In addition, you can continue to access array designs based on past genome data builds, which can be particularly useful for comparisons to prior studies.

Applications & References

Applications References
ChIP-chip Performance
To learn more about the performance of the NimbleGen ChIP-chip platform, review the first ever objective analysis of tiling array platforms, amplification procedures, and signal detection algorithms in a simulated ChIP-chip experiment. Johnson DS, et al. “Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets,” Genome Res.: 18:393-403 (2008)
Transcription Factor Binding
Analyze transcription factor binding from human to A. thaliana using targeted promoter arrays or map factor binding across the entire genome of your choice in an unbiased manner. The combination of isothermal long oligonucelotide probes and high-density make detecting ultra-low fold-changes (less than 2-fold) a reality. Hatzis P, et al. “Genome-wide pattern of TCF7L2/TCF4 chromatin occupancy in colorectal cancer cells,” Mol. Cell Biol.: 28(8):2732-44 (2008)
Krishnakumar R, et al. “Reciprocal binding of PARP-1 and histone H1 at promoters specifies transcriptional outcomes,” Science: 319(5864), 819-821 (2008)
Parelho V, et al. “Cohesins functionally associate with CTCF on mammalian chromosome arms,” Cell: 132(3), 422-433 (2008)
Johnson DS, et al. “Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets, Genome Research: 18(3), 393-403, (2008)
Xu X, et al. “A comprehensive ChIP-chip analysis of E2F1, E2F4, and E2F6 in normal and tumor cells reveals interchangeable roles of E2F family members,” Genome Research: 17(11), 1550-1561, (2007)
Chromatin Structure
Interrogate chromatin structure by using ChIP-chip to analyze histone modifications, histone replacement patterns, and the precise positioning of individual nucleosomes at unprecedented resolution. Due to the inherent flexibility of NimbleGen ChIP-chip arrays, resolution can be defined as low as 1bp to reliably detect even the smallest perturbations within chromatin structure. Kirmizis A, et al. “Arginine methylation at histone H3R2 controls deposition of H3K4 trimethylation,” Nature: 449(7164), 928-932 (2007)
Rinn JL, et al., “Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs,' Cell: 129(7), 1311-1323 (2007)
Heintzman ND, et al. “Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome,”Nature Genetics: 39(3), 311-318 (2007)
Ozsolak F, et al. “High-throughput mapping of the chromatin structure of human promoters,” Nature Biotechnology: 25(2), 244-248 (2007)
Discovery of Genomic Elements
Use ChIP-chip as a tool for identifying and characterizing novel genomic elements and active promoters and enhancers by performing ChIP against RNA polymerase, transcriptional pre-initiation components, and histone modifications. Parelho V, et al. “Cohesins functionally associate with CTCF on mammalian chromosome arms,” Cell: 132(3):422-33 (2008)
Kim TH, et al. “Analysis of the vertebrate protein CTCF-binding sites in the human genome,” Cell: 128, 1231-1245 (2007)
Barrera LO, et al. “Genome-wide mapping and analysis of active promoters in mouse embryonic stem cells and adult organs,” Genome Research: 18(1), 46-59 (2007)
Kim TH, et al. “A high-resolution map of active promoters in the human genome,” Nature: 436(7052), 876-880 (2005)
DNAse Hypersensitivity
Detect and characterize regions of genomic DNA that are highly accessible to cleavage by DNase-I to identify open chromatin regions that permit gene expression. Boyle PA, et al. “High-resolution mapping and characterization of open chromatin across the genome,” Cell: 132, 311-322 (2008)
Follows GA, et al. “Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sites,” Genome Research: 16, 1310-1319 (2006)
Crawford GE, et al., “DNase-chip: a high resolution method to identify DNase-I hypersensitive sites using tiled microarrays,” Nature Methods: 3(7), 503-509 (2006)
Sabo PJ, et al. “Genome-scale mapping of DNase I sensitivityin vivousing tiling DNA microarrays,” Nature Methods: 3(7), 511-518 (2006)

Workflows

ChIP-chip Delivery WorkflowDelivery Workflow Icon

  1. Purchase a NimbleGen catalog array or custom designed array of your choice.
  2. Prepare your ChIP-chip samples in your laboratory.
  3. Label the immunoprecipitated (IP) and Input DNA samples with Cy5 and Cy3 respectively, using the NimbleGen Dual-Color DNA Labeling Kit.
  4. Pool and hybridize the samples to the array using a NimbleGen Hybridization Kit and NimbleGen Hybridization System 4 or 12.
  5. Wash the arrays using the NimbleGen Wash Buffer Kit and the NimbleGen Microarray Dryer.
  6. Scan the array using the 2-μm, high-resolution NimbleGen MS 200 Microarray Scanner.
  7. Analyze the data using NimbleScan software and visualize your ChIP-chip results using SignalMap software.

ChIP-chip Service WorkflowService Workflow Icon

  1. Purchase NimbleGen catalog arrays or custom designed arrays of your choice.
  2. Prepare your ChIP-chip samples in your laboratory and then ship them to Roche NimbleGen.
  3. Roche NimbleGen will manufacture and process the arrays from labeling through data analysis.
  4. Roche NimbleGen will send you raw and analzyed data, genome annotation, and promoter reports.
  5. Visualize your results using SignalMap software.

Availability

Delivery and Service Workflows are not available for every ChIP-chip array design. Please consult the Availability section on this page for a complete list.

Availability

The 2.1M, 3x720K, 385K, and 4x72K array formats and the Delivery and Service workflows are not available for every ChIP-chip array design. Use the table below to identify the availability of different formats and workflows across our ChIP-chip design offerings.

Whole-Genome Designs
 
2.1M

3x720K

385K

4x72K
A. thaliana N/A N/A Service or Delivery Workflow N/A
C. elegans Service or Delivery Workflow N/A Service or Delivery Workflow N/A
D. melanogaster Service or Delivery Workflow N/A Service or Delivery Workflow N/A
E. coli N/A N/A Service or Delivery Workflow N/A
Human Service or Delivery Workflow N/A N/A N/A
Mouse Service or Delivery Workflow N/A N/A N/A
Rat Service or Delivery Workflow N/A N/A N/A
S. cerevisiae N/A N/A Service or Delivery Workflow N/A
Custom Service or Delivery Workflow Service or Delivery Workflow Service or Delivery Workflow Delivery Workflow
Promoter Designs
 
2.1M

3x720K

385K

4x72K
A. thaliana N/A N/A Service or Delivery Workflow N/A
Human Service or Delivery Workflow Service or Delivery Workflow Service or Delivery Workflow N/A
Mouse Service or Delivery Workflow Service or Delivery Workflow Service or Delivery Workflow N/A
Rat N/A Service or Delivery Workflow Service or Delivery Workflow N/A
Custom Service or Delivery Workflow Service or Delivery Workflow Service or Delivery Workflow Delivery Workflow
Targeted Designs
 
2.1M

385K

4x72K
Dog N/A Service or Delivery Workflow N/A
Human N/A Service or Delivery Workflow Delivery Workflow
Custom Service or Delivery Workflow Service or Delivery Workflow Delivery Workflow
KEY:
Service or Delivery Workflow - Delivery OR Service Workflow
Delivery Workflow - Delivery Workflow Only
Service Workflow - Service Workflow Only
N/A - Not Available

Literature

Brochures & Datasheets

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Application Notes & Whitepapers

For a complete listing of literature covering all Roche NimbleGen products and services please visit our literature page.

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