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Render Timestamp: 2024-11-01T10:57:40.996Z
Commit: 23cb9f61fe67e1e9093fd644a533c4ff516a6463
XML generation date: 2024-09-20 06:20:05.525
Product last modified at: 2024-10-28T14:30:10.994Z
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PDP - Template Name: ChIP Kit
PDP - Template ID: *******ae3c2cc

DNA Purification Buffers and Spin Columns (ChIP, CUT&RUN, CUT&Tag) #14209

    Product Information

    Product Usage Information

    Use as directed in the respective SimpleChIP® Chromatin IP kit, the CUT&RUN Assay kit, and the CUT&Tag Assay kit protocols. Please note that if following the SimpleChIP® Chromatin protocol or the CUT&Tag protocol, there will be excess DNA Binding Buffer (#10007) to accommodate the CUT&RUN protocol.

    Storage

    Store at room temperature. Components are stable for 12 months upon receipt when stored properly.

    Product Description

    This product is offered to enable DNA purification using spin columns with our CUT&RUN Assay Kit (#86652).

    This product also is offered to conveniently provide additional buffer reagents when using our SimpleChIP® (#9002, #9003) and SimpleChIP® Plus (#9004, #9005) Enzymatic Chromatin IP Kits, SimpleChIP® Sonication Chromatin IP Kit (#56383), and CUT&Tag Assay Kit (#77552). These kits provide all the reagents required for performing the respective assays, however there are instances where extra buffers are desired.

    The DNA purification columns combine the convenience of spin-column technology with the selective binding properties of a uniquely designed silica membrane that allows for efficient recovery of DNA and removal of protein contaminants without the need for phenol/chloroform extractions and ethanol precipitations. After DNA purification, the enrichment of particular DNA sequences can be analyzed by a variety of methods.
    For Research Use Only. Not For Use In Diagnostic Procedures.
    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    SimpleChIP is a registered trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit our Trademark Information page.