ChIP H3K27me3 Sheep Human

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Get tips on using ChIP-IT® Express Chromatin Immunoprecipitation Kits to perform ChIP Human - THP-1

Products Active Motif ChIP-IT® Express Chromatin Immunoprecipitation Kits

Get tips on using ChIP-IT® Express Chromatin Immunoprecipitation Kits to perform ChIP Human - HEK 293

Products Active Motif ChIP-IT® Express Chromatin Immunoprecipitation Kits
EZ-ChIP™ Product

Get tips on using EZ-ChIP™ to perform ChIP Rat - Mesenteric arteries

Products Merck Millipore EZ-ChIP™

Get tips on using ChIP-IT® Express Chromatin Immunoprecipitation Kits to perform ChIP Human - Fibroblast cell lines

Products Active Motif ChIP-IT® Express Chromatin Immunoprecipitation Kits

Get tips on using EZ‐ChIP™ Assay Kit (Cat#17–371) to perform ChIP Human - HeLa

Products Merck Millipore EZ‐ChIP™ Assay Kit (Cat#17–371)

Get tips on using EZ-Magna ChIP™ G - Chromatin Immunoprecipitation Kit to perform ChIP Human - Kupffer Cells

Products Merck Millipore EZ-Magna ChIP™ G - Chromatin Immunoprecipitation Kit

DNA-protein interactions are studied by using ChIP. The basic steps in this technique are crosslinking, sonication, immunoprecipitation, and analysis of the immunoprecipitated DNA. During ChIP, if chromatin is under-fragmented or fragments are too large which can lead to the increased background and lower resolution. Shorter cross-linking times (5-10 min) and/or lower formaldehyde concentrations (<1%) may improve shearing efficiency. If Chromatin is over-fragmented, then optimize shearing conditions for each cell type to improve ChIP efficiency. Over-sonication of chromatin may disrupt chromatin integrity and denature antibody epitopes. If you do not see any product or very little product in the input PCR reactions, add 5–10 μg chromatin per IP.

Proteins ChIP Mouse 3T3-L1 cells

DNA-protein interactions are studied by using ChIP. The basic steps in this technique are crosslinking, sonication, immunoprecipitation, and analysis of the immunoprecipitated DNA. During ChIP, if chromatin is under-fragmented or fragments are too large which can lead to the increased background and lower resolution. Shorter cross-linking times (5-10 min) and/or lower formaldehyde concentrations (<1%) may improve shearing efficiency. If Chromatin is over-fragmented, then optimize shearing conditions for each cell type to improve ChIP efficiency. Over-sonication of chromatin may disrupt chromatin integrity and denature antibody epitopes. If you do not see any product or very little product in the input PCR reactions, add 5–10 μg chromatin per IP.

Proteins ChIP Mouse Gonadotrope cell lines

Get tips on using EpiTect ChIP qPCR Assays to perform ChIP Rat - Brain

Products Qiagen EpiTect ChIP qPCR Assays

Get tips on using EpiTect ChIP OneDay Kit to perform ChIP Mouse - MIN6

Products Qiagen EpiTect ChIP OneDay Kit

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