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17-10522 Magna Nuclear RIP™ (Native)
Nuclear RNA-Binding Protein Immunoprecipitation Kit

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24 assays  Kit capacity: 24 RNA-binding protein immunoprecipitation assays using a native (non-cross-linked) nuclear lysate
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      Key Specifications Table

      Key Applications
      RIP, Protein Interaction Assays
      Catalogue Number17-10522
      Trade Name
      • Magna Nuclear RIP
      DescriptionMagna Nuclear RIP™ (Native)
      Nuclear RNA-Binding Protein Immunoprecipitation Kit
      OverviewFeatures and Advantages

      • Generates native chromatin to allow analysis of a variety of chromatin-associated RNAs
      • Flexible, scalable input requirements: Recover RNA from millions of cells or as few as 100,000 cells (native)
      • Magnetic protein A/G bead blend and optimized buffer system results in low backgrounds and high signal-to-noise ratios
      • Suitable for analysis by RT-qPCR or RIP-seq
      • Complete set of reagents and detailed protocol to enable first-time success

      Magna Nuclear RIP™ Kits are specially designed to allow the discovery and analysis of a variety of chromatin associated RNAs such as long non-coding RNAs, enhancer RNAs and miRNAs . These chromatin-associated RNAs often regulate gene expression and can be analyzed with applications including quantitative reverse transcription polymerase chain reaction (RT-PCR), microarray analysis (RIP-chip) and next generation sequencing (RIP-Seq).

      Nuclear RIP can be performed using chromatin that has interactions stabilized by formaldehyde treatment (cross-linked) or chromatin that has not been treated with a cross linking reagent (native). While both of these approaches are similar in that they are designed to recover chromatin associated RNA, the reagents used and the details of the protocol and types of interactions typically detected are different. Native RIP is expected to recover high affinity, more direct interactions between proteins encoded RNA binding motifs and candidate RNAs. In contrast, nuclear RIP with cross-linked chromatin can capture higher molecular weight complexes in in vivo configurations with possibly lower affinities. For less well understood proteins and protein complexes often both approaches are used.

      The kit described here is for the native approach. If a cross-linked approach is of interest please visit the product page for the Magna Nuclear RIP
      (Cross-Linked) Kit , catalogue # 17-10520or the EZ-Magna Nuclear RIP (Cross-Linked) Kit, catalogue # 17-10521.
      Materials Required but Not DeliveredReagents
      • Cells or tissue, stimulated or treated as needed for the experimental system
      • Antibody of interest for RNA-binding protein immunoprecipitation (RIP)
      • Negative Control Antibody
      • PBS (RNase free)
      • (e.g. Fisher, Cat. # BP2438-4)
      • TRIzol® Reagent Life Technologies Cat. #15596-026) or similar organic extraction reagent
      • Chloroform (e.g. Fisher, Cat. # BP1145)
      • Isopropanol (molecular biology grade)
      • 100% Ethanol (molecular biology grade)
      • Precipitation Carrier (e.g. Pellet Paint® Co-Precipitant (125 reactions, EMD Millipore Cat. # 69049) or linear Acrylamide (5mg/mL) if samples are intended for Next Gen Sequence library preparation.
      • Nuclease Free Water
      • Liquid nitrogen (Optional)
      • Reagents for qRT-PCR Analysis and/or Reagents for RNA-Seq Library Construction (optional)

      • 1 mL Syringes
      • 27G Needles
      • Dounce homogenizer (loose pestle, necessary for tissue samples but optional for cultured cells)
      • Magnetic Separation Stand (e.g. Magna GrIP™ Rack 8 well, (Cat. # 20-400) or PureProteome™ Magnetic Stand, (Cat. # LSKMAGS08)
      • Vortex mixer
      • Rotating wheel/platform
      • Microcentrifuge capable of up to 12,000 x g
      • -80°C freezer
      • Variable temperature water bath or incubator
      • Rotating microtube mixer
      • Real-time PCR thermal cycler
      Product Information
      • Nuclei Isolation Buffer
      • RIP Lysis Buffer
      • Protein A/G Magnetic Beads
      • RIP Lysis Buffer
      • 0.5M EDTA
      • DNase I (RNase Free) 2 U/μL
      • DNase I Reaction Buffer
      • Protease Inhibitor Cocktail III, Animal Free
      • RNAse Inhibitor
      PresentationTwo boxes containing key reagents for generation of native nuclear lysates and performance of 24 individual RNA-binding protein immunoprecipitation (RIP) reactions.
      Quality LevelMQ100
      ApplicationMagna Nuclear RIP (Native) RNA-Binding Protein Immunoprecipitation Kit is designed for the analysis of chromatin associated RNA such lncRNAs, enhancer RNAs and miRNAs.
      Key Applications
      • RNA Binding Protein Immunoprecipitation (RIP)
      • Protein Interaction Assays
      Biological Information
      Physicochemical Information
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Usage Statement
      • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
      Storage and Shipping Information
      Storage ConditionsUpon receipt, store components at the temperatures indicated on the labels.
      Kit components are stable for 6 months from date of shipment when stored as directed.
      Packaging Information
      Material Size24 assays
      Material PackageKit capacity: 24 RNA-binding protein immunoprecipitation assays using a native (non-cross-linked) nuclear lysate
      Transport Information
      Supplemental Information
      Global Trade Item Number
      Catalog Number GTIN
      17-10522 04055977127379