Pierce™ Magnetic RNA-Protein Pull-Down Kit
Pierce™ Magnetic RNA-Protein Pull-Down Kit
Thermo Scientific™

Pierce™ Magnetic RNA-Protein Pull-Down Kit

The Thermo Scientific Pierce Magnetic RNA-Protein Pull-Down Kit provides researchers with a streamlined, robust method to enrich protein-RNA interactions usingRead more
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Catalog number 20164
Price (USD)
954.00
Each
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Price (USD)
954.00
Each
Add to cart
The Thermo Scientific Pierce Magnetic RNA-Protein Pull-Down Kit provides researchers with a streamlined, robust method to enrich protein-RNA interactions using end-labeled RNA as the bait.

Features of the Magnetic RNA-Protein Pull-Down Kit:

Direct – capture ribonucleoprotein complexes directly with end-labeled RNA; does not use or require antibodies for pull-down
Easy to use – no spin cups or centrifugation necessary for the enrichment of RBP; procedure streamlined for minimal hands-on time (less than 3 hours) after RNA labeling reaction
Flexible – use in vitro transcribed RNA or synthetic RNA for labeling of various lengths and complexity; proteins successfully enriched using endogenous, over-expressed, and in vitro translated lysates
Specific – low bead background; unrelated RNA or mutated RNA does not significantly enrich specified RBPs
Economical – less expensive than purchasing commercially synthesized end-labeled RNA, magnetic beads, and reagents separately
Complete – contains both labeling and enrichment modules with buffers necessary for assay; positive control RNA, negative control RNA, and RBP antibody included

The Magnetic RNA-Protein Pull-Down Kit provides reagents to efficiently enrich RNA Binding Proteins (RBPs) using RNA end-labeled with desthiobiotin and streptavidin magnetic beads. The complete kit contains sufficient reagents for 20 RNA labeling reactions and 20 protein-RNA pull-down assays. This direct enrichment of the protein-RNA interaction provides an alternative to antibody capture of protein-RNA complexes or moieties incorporated into the nucleic acid. An added advantage to the kit is that it includes validated controls for both the labeling and pull-down assay. The kit is amenable to several downstream applications, including Western blotting and Mass Spectrometry (MS).

Includes:
Complete kit contains the Pierce RNA 3'-End Desthiobiotinylation Kit, positive and negative RNA controls, nucleic-acid compatible streptavidin magnetic beads, and buffers for RBP enrichment and elution

Requires:
User-supplied RNA and lysate (experimental sample)

Applications:
• Mutational analysis
• Structure function analysis
• Identification of RNA:Protein interactions
• MS analysis of unknown RNA:protein binding pairs or complexes

Utilizing labeled RNA as bait for RNA-binding protein enrichment is advantageous over antibody enrichment in that it captures the interaction directly. Included in this kit is the Pierce RNA 3'-End Desthiobiotinylation Kit, which uses T4 RNA ligase to attach a single cytidine bisphosphate nucleotide to the 3'-ends of single-stranded RNA. Desthiobiotin may be used for detection or as an elutable affinity handle. The length of the spacer between the nucleotide and desthiobiotin has been optimized for efficient attachment to the beads without compromising the accessibility of the RNA to protein.

The procedure for enrichment of RNA binding proteins has been optimized for ease-of-use. The labeled RNA is first captured to the beads to orient the RNA for protein binding. RNA-bound beads are then equilibrated in Protein RNA Binding buffer before protein lysate is added. After washing, sample can be eluted using either nondenaturing Biotin Elution Buffer or SDS-PAGE loading buffer. Eluted samples are ready for a variety of downstream applications, including Western blotting or Mass spectrometry.

The control system for the pull-down assay utilizes 3'-untranslated region androgen receptor (AR) RNA, poly(A)25 RNA, and mammalian cell lysate. The proximal 3'-untranslated region (UTR) of androgen receptor RNA contains UC-rich regions for HuR and Poly(C) Binding Proteins (CP1 and 2). These RNA binding proteins regulate mRNA stability (HuR) and mRNA turnover and translation (CP1 and 2). The negative control RNA, poly(A)25 RNA, does not contain HuR or poly(C) BP binding sites.

Related Products
Pierce™ Magnetic RNA-Protein Pull-Down Kit
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Capacity (Metric)50 pmol of RNA per Reaction
Product LinePierce™
Quantity1 Kit
TypeRNA-Protein Pull Down Kit
Sufficient For20 Reactions
FormatKit
Unit SizeEach
Contents & Storage
Sufficient For: 20 RNA-protein complex pull-down reactions
• Pierce Nucleic Acid-Compatible Streptavidin Magnetic Beads, 1 mL (store at 4°C)
• RNA Capture Buffer (1X), 10 mL (store at 4°C)
• Tris (20 mM, pH 7.5), 5 mL (store at 4°C)
• Protein-RNA Binding Buffer (10X), 1 mL (store at 4°C)
• Wash Buffer (1X), 10 mL (store at 4°C)
• Biotin Elution Buffer, 1.5 mL (store at 4°C)
• HuR Monoclonal Antibody (Mouse), 50 μL (store at 4°C)
• Positive RNA Control (AR RNA), 250 pmol (store at -20°C)
• Negative RNA Control (polyA25 RNA), 250 pmol (store at -20°C)
• Pierce RNA 3' End Desthiobiotinylation Kit (part number 20163; store at -20°C)

Frequently asked questions (FAQs)

Can I use Coomassie or silver staining to detect proteins isolated with the Pierce Magnetic RNA-Protein Pull-Down Kit (Cat. No. 20164)?

Proteins isolated with the Magnetic RNA-Protein Pull-Down Kit cannot be detected by Coomassie or silver staining. Gels can be used for detection depending on the amount of total protein used in the experiment. If the protein of interest has an antibody available, it can usually be detected via western blotting. Finally, if the protein isolated is unknown, it can be analyzed by mass spectrometry.

After using the Magnetic RNA-Protein Pull-Down Kit, I would like to analyze my elution fraction by mass spectrometry (MS). How can I do this?

The elution fraction is compatible with preparation of peptides. Samples may be processed using the Mass Spec Sample Prep Kit for Cultured Cells (Cat. No. 89840). Alternatively, the elution fraction may be separated by denaturing PAGE. Bands of interest can be excised, and digested using the In-Gel Tryptic Digestion Kit (Cat. No. 89871).

I am using the Magnetic RNA-Protein Pull-Down Kit and am getting a low signal on my western blot. What is the problem?

Here are the possible causes and solutions:

- Insufficient signal: Increase amount of secondary antibody; Use a more sensitive chemiluminescent detection (e.g., SuperSignal Dura or SuperSignal Femto Chemiluminescent Substrate).
- Poor antibody quality: Pre-screen antibody with cell lysate; Include cell lysate as a control on western blot.
- Protein was insufficient in lysate: Increase amount of sample; Identify alternate source of protein; Use a more concentrated lysate.

With the Magnetic RNA-Protein Pull-Down Kit, I am getting high non-specific binding of the RNA-binding protein. Why is this?

Here are possible causes and solutions:

- Binding reaction was not optimized: Optimize incubation time, temperature, salt and detergent for binding reactions.
- Insufficient washing stringency: Increase stringency of wash buffer; add salt and/or detergent.
- Ratio of labeled RNA to lysate was not optimized: Titrate labeled RNA with protein lysate; Reduce the concentration of lysate to ~2mg/mL.

I got no recovery of the RNA-binding protein when I used the Magnetic RNA-Protein Pull-down Kit. What should I do?

Here are possible causes and solutions:

- Insufficient amount of target protein in the sample: Increase amount of sample.
- Sample was not compatible with the binding reaction: Buffer exchange sample using Zeba Desalting Columns.
- Binding reaction was not optimized: Optimize incubation time, temperature, salt and detergent for binding reactions; Titrate amount of labeled RNA to protein lysate; Use a more concentrated lysate.
- RNA binding protein had low affinity for labeled RNA: Add crosslinking reagent (e.g., UV, etc.) after protein has bound RNA.