SimpleChIP® Human GATA-6 Promoter PrimersProduct information
|500 µl (250 PCR reactions)||-||Unavailable in your region|
SimpleChIP® Control PCR Primers
SimpleChIP® Human GATA-6 Promoter Primers #5550
|5550S||500 µl (250 PCR reactions)||---||In Stock||---|
|5550||carrier free and custom formulation / quantity||email request|
Product is assembled upon order. Please allow up to three business days for your product to be processed.
|Applications||Reactivity||Primer Anneal / Extension||PCR Product Length|
|Chromatin IP||Human||65 °C||199 bp|
SimpleChIP® Human GATA-6 Promoter Primers contain a mix of forward and reverse PCR primers that are specific to a region of the human GATA-6 promoter. These primers can be used to amplify DNA that has been isolated using chromatin immunoprecipitation (ChIP). Primers have been optimized for use in SYBR® Green quantitative real-time PCR and have been tested in conjunction with SimpleChIP® Enzymatic Chromatin IP Kits #9002 and #9003 and ChIP-validated antibodies from Cell Signaling Technology. The GATA-6 gene promoter is bivalent in stem cells, containing both histone H3 tri-methyl Lys4 and tri-methyl Lys27 epigenetic marks. When the GATA-6 gene is activated during endoderm development, the promoter becomes monovalent, as the histone H3 tri-methyl Lys27 mark is removed and the tri-methyl Lys4 mark is retained.
Directions For Use
- Label the appropriate number of PCR tubes or PCR plates compatible with the model of real-time PCR machine to be used. PCR reactions should be performed in duplicate and should include a tube with no DNA to control for contamination, and a serial dilution of a 2% total input chromatin DNA (undiluted, 1:5, 1:25, 1:125), which is used to create a standard curve and determine amplification efficiency.
- Add 2 µl of the appropriate ChIP DNA sample to each tube or well of the PCR plate.
- Prepare a master PCR reaction mix as described below. Add enough reagents for two extra reactions to account for loss of volume. Add 18 µl of the master PCR reaction mix to each PCR reaction tube or well of the PCR plate.
Reagent Volume for 1 PCR Reaction (20 µl)
|Nuclease-free H2O||6 µl|
|5 µM SimpleChIP® Primers||2 µl|
|2X SYBR® Green Reaction Mix||10 µl|
- Start the following PCR reaction program:
- Initial Denaturation: 95°C for 3 min.
- Denaturation: 95°C for 15 sec.
- Anneal and Extension: Primer-specific temp. for 60 sec.
- Repeat steps b and c for a total of 40 cycles.
- Analyze quantitative PCR results using software provided with the real-time PCR machine.
SimpleChIP® Human GATA-6 Promoter Primers were tested on DNA isolated from cross-linked cells using the SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003. Real-time PCR was performed in duplicate on a serial dilution of 2% total input DNA (20 ng, 4 ng, 0.8 ng, and 0.16 ng) using a real-time PCR detection system and SYBR® Green reaction mix. The PCR amplification efficiency (E) and correlation coefficient (R2) were calculated based on the corresponding threshold cycle (CT) of each dilution sample during 40 cycles of real-time PCR (95°C denaturation for 15 sec, 65°C anneal/extension for 60 sec).
PCR product melting curves were obtained for real-time PCR reactions performed using SimpleChIP® Human GATA-6 Promoter Primers. Data is shown for both duplicate PCR reactions using 20 ng of total DNA. The melt curve consists of 80 melt cycles, starting at 55°C with increments of 0.5°C per cycle. Each peak is formed from the degradation of a single PCR product.
The chromatin immunoprecipitation (ChIP) assay is a powerful and versatile technique used for probing protein-DNA interactions within the natural chromatin context of the cell (1,2). This assay can be used to either identify multiple proteins associated with a specific region of the genome or to identify the many regions of the genome bound by a particular protein (3-6). ChIP can be used to determine the specific order of recruitment of various proteins to a gene promoter or to "measure" the relative amount of a particular histone modification across an entire gene locus (3,4). In addition to histone proteins, the ChIP assay can be used to analyze binding of transcription factors and co-factors, DNA replication factors, and DNA repair proteins. When performing the ChIP assay, cells are first fixed with formaldehyde, a reversible protein-DNA cross-linking agent that "preserves" the protein-DNA interactions occurring in the cell (1,2). Cells are lysed and chromatin is harvested and fragmented using either sonication or enzymatic digestion. Fragmented chromatin is then immunoprecipitated with antibodies specific to a particular protein or histone modification. Any DNA sequences that are associated with the protein or histone modification of interest will co-precipitate as part of the cross-linked chromatin complex and the relative amount of that DNA sequence will be enriched by the immunoselection process. After immunoprecipitation, the protein-DNA cross-links are reversed and the DNA is purified. Standard PCR or quantitative real-time PCR are often used to measure the amount of enrichment of a particular DNA sequence by a protein-specific immunoprecipitation (1,2). Alternatively, the ChIP assay can be combined with genomic tiling micro-array (ChIP on chip) techniques, high throughput sequencing (ChIP-Seq), or cloning strategies, all of which allow for genome-wide analysis of protein-DNA interactions and histone modifications (5-8). SimpleChIP® primers have been optimized for amplification of ChIP-isolated DNA using real-time quantitative PCR and provide important positive and negative controls that can be used to confirm a successful ChIP experiment.
- Orlando, V. (2000) Trends Biochem Sci 25, 99-104.
- Kuo, M.H. and Allis, C.D. (1999) Methods 19, 425-33.
- Agalioti, T. et al. (2000) Cell 103, 667-78.
- Soutoglou, E. and Talianidis, I. (2002) Science 295, 1901-4.
- Mikkelsen, T.S. et al. (2007) Nature 448, 553-60.
- Lee, T.I. et al. (2006) Cell 125, 301-13.
- Weinmann, A.S. and Farnham, P.J. (2002) Methods 26, 37-47.
- Wells, J. and Farnham, P.J. (2002) Methods 26, 48-56.
Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know!
- 9007 ChIP-Grade Protein G Agarose Beads
- 9006 ChIP-Grade Protein G Magnetic Beads
- 9002 SimpleChIP® Enzymatic Chromatin IP Kit (Agarose Beads)
- 9003 SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads)
- 9733 Tri-Methyl-Histone H3 (Lys27) (C36B11) Rabbit mAb
- 9751 Tri-Methyl-Histone H3 (Lys4) (C42D8) Rabbit mAb
This product is intended for research purposes only. The product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.
SYBR is a registered trademark of Life Technologies Corporation.
SimpleChIP is a registered trademark of Cell Signaling Technology, Inc.
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.