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#P-2010-48 EpiQuik Acetyl_Histone H3 ChIP Kit
Product name : EpiQuik Acetyl_Histone H3 ChIP Kit
Catalog number : P-2010-48
Quantity: 48 reactions
Supplier name : EpigenTek
Data sheet: Ask more or other datasheet now !
More Details about
The EpiQuik™ Acetyl-Histone H3 ChIP Kit is a convenient package of tools that allows the experimenter to investigate interactions of histone H3 acetylation and DNA in vivo efficiently. The entire procedure can be completed within 5 hours and produces far superior results than any competitor kits. The EpiQuik™ Acetyl-Histone H3 ChIP Kit is suitable for combining the specificity of immunoprecipitation with qualitative and quantitative PCR, MS-PCR, DNA sequencing, and southern blot, as well as DNA microarray.
WHY CHOOSE THE EPIQUIK™ ACETYL-HISTONE H3 ChIP KIT?
- The fastest procedure available, which can be finished within 5 hours.
- Strip microwell format makes the assay flexible: manual or high throughput.
- Columns for DNA purification are included: save time and reduce labor.
- Compatible with all DNA amplification-based approaches.
- Simple, reliable, and consistent assay conditions.
The EpiQuik™ Acetyl-Histone H3 ChIP Kit contains all reagents required for carrying out a successful chromatin immunoprecipitation for acetyl-histone H3 from mammalian cells. Particularly, this kit includes a ChIP-grade acetyl-histone H3 antibody and a negative control normal mouse IgG. Chromatin in the cells is extracted, sheared, and added into the microwell immobilized with the antibody. Acetyl-histone H3 protein-DNA complex is captured by the antibody and DNA is released and purified through the specifically designed Fast-Spin Column. Eluted DNA can be used for various down-stream applications.
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WP2359: Parkin-Ubiquitin Proteasomal System pathway
Related Genes :
 Aberrant histone methylation in the patients with immune thrombocytopenia.
 Aberrant histone modification in peripheral blood B cells from patients with systemic sclerosis.
 Aberrant histone acetylation and methylation levels in woman with endometriosis.
 Abnormal histone modifications in PBMCs from patients with psoriasis vulgaris.
 Abnormal histone modification patterns in lupus CD4+ T cells.
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