17-10521
EZ-Magna NuCLEAR™ RIP (Cross-Linked) Nuclear RNA-Binding Protein Immunoprecipitation Kit
EZ-Magna Nuclear RIP (Cross-Linked) RNA-Binding Protein Immunoprecipitation Kit is designed for the analysis of chromatin associated RNA such lncRNAs, enhancer RNAs and miRNAs.
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Synonym(s):
Magnetic RNA-BP Immunoprecipitation, RNA-Binding Protein Immunoprecipitation
UNSPSC Code:
12161503
eCl@ss:
32161000
NACRES:
NA.32
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Quality Level
manufacturer/tradename
Magna Nuclear RIP
technique(s)
RIP: suitable
activity assay: suitable (protein interaction)
immunoprecipitation (IP): suitable
shipped in
dry ice
Related Categories
General description
Features and Advantages
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. Cross-linked can capture higher molecular weight complexes in in vivo configurations with possibly lower affinities. In contrast native RIP is expected to recover high affinity, more direct interactions between proteins encoded RNA binding motifs and candidate RNAs. For less well understood proteins and protein complexes often both approaches are used.
The kit described here is for the cross-linked approach. If a native approach is of interest please visit the product page for the Magna Nuclear RIP (Native) Kit, catalogue # 17-10522 or the EZ-Magna Nuclear RIP (Native) Kit, catalogue # 17-10523.
- Generates cross-linked 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 5,000 cells
- 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. Cross-linked can capture higher molecular weight complexes in in vivo configurations with possibly lower affinities. In contrast native RIP is expected to recover high affinity, more direct interactions between proteins encoded RNA binding motifs and candidate RNAs. For less well understood proteins and protein complexes often both approaches are used.
The kit described here is for the cross-linked approach. If a native approach is of interest please visit the product page for the Magna Nuclear RIP (Native) Kit, catalogue # 17-10522 or the EZ-Magna Nuclear RIP (Native) Kit, catalogue # 17-10523.
Packaging
Kit capacity: 24 RNA-binding protein immunoprecipitation assays using a cross-linked nuclear lysate
Components
10X Glycine
10X PBS
Nuclei Isolation Buffer
RIP Cross-Linked Lysis Buffer
Protein A/G Magnetic Beads
Nuclear RIP Dilution Buffer
Low Salt Wash Buffer
High Salt Wash Buffer
LiCl Wash Buffer
TE Buffer
RIP Elution Buffer
10% SDS
0.5 M EDTA
DNase I (RNase Free)
DNase I Supplement
DNase I Reaction Buffer
Protease Inhibitor Cocktail III, Animal Free
RNAse Inhibitor
Proteinase K
Control Antibodies and Primers
Normal Mouse IgG Negative Control Antibody
Anti-EZH2 Positive Control Antibody
NEAT1 Positive Control Primers
U1 snRNA Negative Control Primers
10X PBS
Nuclei Isolation Buffer
RIP Cross-Linked Lysis Buffer
Protein A/G Magnetic Beads
Nuclear RIP Dilution Buffer
Low Salt Wash Buffer
High Salt Wash Buffer
LiCl Wash Buffer
TE Buffer
RIP Elution Buffer
10% SDS
0.5 M EDTA
DNase I (RNase Free)
DNase I Supplement
DNase I Reaction Buffer
Protease Inhibitor Cocktail III, Animal Free
RNAse Inhibitor
Proteinase K
Control Antibodies and Primers
Normal Mouse IgG Negative Control Antibody
Anti-EZH2 Positive Control Antibody
NEAT1 Positive Control Primers
U1 snRNA Negative Control Primers
Physical form
Two boxes containing key reagents for generation of cross linked nuclear lysates and performance of 24 individual RNA-binding protein immunoprecipitation (RIP) reactions. Plus box containing positive and negative control antibodies and qPCR primers.
Storage and Stability
Upon 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.
Kit components are stable for 6 months from date of shipment when stored as directed.
Legal Information
NuCLEAR is a trademark of Sigma-Aldrich Co. LLC
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2
WGK
WGK 3
Regulatory Information
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Certificates of Analysis (COA)
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