manufacturer/tradename
Magna ChIP®
technique(s)
immunoprecipitation (IP): suitable
shipped in
dry ice
Quality Level
相关类别
General description
Features & Benefits
- Complete set of materials for up to 96 ChIP reactions
- Protein A+G bead blend for ChIP with a broader range of antibodies than A or G alone
- Low Chromatin requirements: 10, 000 to 100, 000 cells per reaction
- Optimized streamlined protocol with only a single buffer for sonication, IP, or wash; and protocols for automated liquid handling systems
- Protocols for using cells or tissues
- Direct analysis of DNA without additional clean-up steps
- Compatible with ChIPAb+ validated antibody and primer sets
Application
Epigenetics & Nuclear Function
Packaging
Physical form
Preparation Note
Other Notes
HT96 Nuclei Isolation Buffer
HT96 ChIP Buffer (Sonication/ChIP/Wash)
Low Stringency IP Wash Buffer
HT96 ChIP Elution Buffer
Proteinase K Solution
Protease Inhibitor Cocktail III
10X Glycine
10X PBS
96 Well ChIP Plate
96 Well Thermal Plate
Plate Seal
Strip Caps
Legal Information
Disclaimer
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
10-13 - German Storage Class 10 to 13
wgk
WGK 3
法规信息
实验方案
Chromatin Immunoprecipitation qPCR for studying gene regulation across conditions.
相关内容
The 3rd edition of An Introduction to Antibodies and Their Applications provides a concise overview of some of the key features for the use of antibodies and immunochemical techniques in biological research. This handy reference guide supplements the techniques described in literature, recorded in general laboratory procedures, and described on individual product data sheets. Antibody design, development, and production are our expertise. Stringent validation of our antibodies is only one component of a comprehensive process we undertake to provide the antibodies most cited by the research community (see section Antibody Quality on page 2 for an in-depth look at our expertise).
New Products: Antibodies, Assays, Small Molecules, Inhibitors, and Proteins
Chromatin immunoprecipitation (ChIP) has been widely adapted for the study of gene-specific and genome-wide distribution of specific DNA- and RNA-binding proteins or protein modifications. Similar to standard protein immunoprecipitation assays, ChIP involves isolation of immunocomplexes using a solid medium, such as agarose or magnetic beads, coupled to either IgG binding recombinant protein A or protein G. In a typical ChIP experiment either protein A or G is selected for enrichment depending on the antibody isotype. However, proteins A and G possess differing affinities for human and mouse IgGs. Complicating this choice, for some antibody isotypes there is affinity for both protein A and G. In addition, we have observed that independent of the isotype the affinity of a specific antibody for protein A or G can vary depending on the specific clone, purification method, and source.
Magna ChIP™ HT96 Kits for high throughput chromatin immunoprecipitation
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