RiboPure™ RNA Purification Kit, blood
RiboPure™ RNA Purification Kit, blood
Invitrogen™

RiboPure™ RNA Purification Kit, blood

The RiboPure™-Blood Kit is for the isolation of high-quality RNA directly from whole blood. The kit combines two methods ofRead more
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Catalog NumberQuantity
AM192840 preps
Catalog number AM1928
Price (EUR)
1.136,00
Each
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Quantity:
40 preps
Price (EUR)
1.136,00
Each
Add to cart
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The RiboPure™-Blood Kit is for the isolation of high-quality RNA directly from whole blood. The kit combines two methods of RNA purification to efficiently remove blood components (protein, heme, genomic DNA, and RNases) that can compromise downstream procedures. The kit includes sufficient reagents for 40 RNA purifications from whole blood samples ranging from 0.3–0.5 mL each. Advantages of the RiboPure™-Blood Kit:

• Purify total RNA directly from whole blood—without prior recovery of WBCs
• Simple, fast procedure—from blood to RNA in less than 30 minutes
• Includes RNAlater™ Solution—store blood samples 3 days or more at room temperature
• Includes DNA-free™ Reagents—to ready RNA for RT-PCR and array analysis

Applications
The RiboPure™-Blood Kit produces high yields of pure RNA directly from whole blood, eliminating the need to isolate WBCs prior to RNA purification. RNA recovered using the RiboPure™-Blood Kit can be used in the most challenging applications, including real-time RT-PCR and array analysis. Average yields of RNA are between 2–4 μg/0.5 mL of whole blood (variation is due to differences in WBC numbers between samples).

Stabilize RNA in whole blood
When collecting blood samples for RNA analysis, storage of the samples prior to RNA isolation is often required. The RiboPure™-Blood Kit contains RNAlater Solution for the stabilization of RNA in whole blood. It also “freezes” the gene expression profile of the cells. Treated samples can be safely stored at ambient temperature for extended periods of time (up to three days or more). Blood samples stored in RNAlater™ Solution yield RNA of comparable quality to blood samples processed directly (see figure).

Simple procedure yields highly pure RNA
The RiboPure™-Blood procedure consists of three steps: 1) addition of Lysis Solution directly to RNAlater-treated or fresh whole blood, 2) initial RNA purification by phenol/chloroform extraction, and 3) final RNA purification on a glass fiber filter. An additional DNase treatment can then be performed with the DNA-free™ Reagents included in the kit. The entire procedure, including DNase treatment, can be completed in less than 1 hour.

Accessory products
The RNA can subsequently be enriched for white blood cell (WBC) mRNA using our GLOBINclear™ Kits to selectively remove globin transcripts. The Mouse RiboPure™-Blood RNA Isolation Kit (Cat. No. AM0951) is also available for the recovery of total RNA—and optionally microRNA—directly from mouse or rat blood. Mouse RiboPure™-Blood includes sample tubes preloaded with RNAlater Solution to prevent RNA degradation and preserve RNA profiles.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Final Product TypeTotal RNA
For Use With (Application)Microarray Analysis, Real-Time Quantitative PCR (qPCR), Reverse Transcriptase PCR (RT-PCR), Northern Blotting
High-throughput CompatibilityNot High-throughput Compatible (Manual)
No. of Reactions40 Preps
Prep Scale100 μL to 1 mL Blood Samples (Medium-scale)
Product LineAmbion™, RiboPure™
Purification Time30 min.
Quantity40 preps
Starting Material AmountUp to 0.5 ml whole blood
Yield4 μg
FormatFilter Cartridge, Tube
Isolation TechnologyOrganic Extraction, Spin Column
Sample TypeBlood
TargetTotal RNA
Unit SizeEach
Contents & Storage
• 25 mL Elution Solution (4°C)
• 40 mL Lysis Solution (4°C)
• 25 mL Acid-Phenol:Chloroform (4°C)
• 5 mL Sodium Acetate Solution (4°C)
• 35 mL Wash Solution 1 (room temperature/4°C)
• 70 mL Wash 2/3 Concentrate (room temperature/4°C)
• 100 mL RNAlater™ Solution (room temperature)
• 40 Filter Cartridges (room temperature)
• 80 Collecion Tubes (room temperature)
• 100 μL DNase I, 8 U/μL (-20°C, frost-free)
• 850 μL 20X DNase Buffer (-20°C)
• 1.2 mL DNase Inactivation Reagent (-20°C)
• 1 mL Formaldehyde Load Dye (-20°C)

This kit contains enough reagents for 40 RNA isolation from 300-500 μL whole blood.
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Certificates

Lot #Certificate TypeDateCatalog Number(s)
2722667Certificate of AnalysisMay 18, 2023AM1928
2712571Certificate of AnalysisApr 29, 2023AM1928
2712423Certificate of AnalysisApr 29, 2023AM1928
2703276Certificate of AnalysisApr 13, 2023AM1928
2703241Certificate of AnalysisApr 13, 2023AM1928
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Safety Data Sheets

Frequently asked questions (FAQs)

The former (Cat. No. AM1928) is for isolation of RNA from human blood and the latter (Cat. No. AM1951) is for isolation of RNA from mouse and rat blood. Both kits have the same columns but differ in protocol and the wash 1 buffer, wash 2/3 buffer, and sodium acetate solutions. We do not recommend using the mouse kit for human blood samples. The mouse kit accommodates the difference in viscosity of mouse/rat vs. human blood and also the higher mouse and rat blood RNA yield. The mouse kit allows recovery of either total RNA containing small RNAs or total RNA depleted of small RNAs based on which protocol in the manual was followed. With the RiboPure Blood Purification Kit, using the standard protocol in the manual, you can isolate total RNA depleted of small RNAs, but with an alternate protocol, you can isolate total RNA containing small RNAs. Alternatively, if you need small RNAs alone, then you should follow the above alternate protocol for isolation of total RNAs containing small RNAs, and then follow Section IVA in the mirVana miRNA Isolation Kit manual (Cat. No AM1560).

Its composition is 0.1 mM EDTA in nuclease-free water.

The column cut-off size is 200 nt. Using a RiboPure kit is not appropriate for miRNA recovery. For miRNA isolation, we would suggest using a mirVana kit, the TRIzol Plus RNA Purification Kit, or the PureLink RNA Micro Kit.

The PureLink RNA Mini Kit provides rapid column-based purification of total RNA, without organic lysis (phenol/chloroform). You can obtain up to 1,000 µg of purified RNA from a single extraction. The RiboPure RNA Purification Kits combine a phenol/guanidine thiocyanate solution with a glass-fiber filter purification method.

Please visit our website for tips for working with blood samples.

Find additional tips, troubleshooting help, and resources within our RNA Sample Collection, Protection, and Isolation Support Center.

Citations & References (5)

Citations & References
Abstract
Stability of cord blood RNA measured by house keeping transcripts: relevance for large-scale studies of childhood leukaemia.
Authors:Olsen M, Madsen HO, Hjalgrim H, Ford A, Schmiegelow K
Journal:Leukemia
PubMed ID:17051240
Comparison of the MagNA pure LC automated system and the RiboPure-Blood RNA manual method for RNA extraction from multiple myeloma bone marrow samples conserved in an RNA stabilizer.
Authors:Garcia-Effron G, Gamarra S, Crooke A, Martínez-Sánchez P, Lahuerta J, Martínez-López J
Journal:Int J Lab Hematol
PubMed ID:17474887
'A total of 62 frozen bone marrow specimens conserved in RNA later (Ambion) were processed using two different extraction methods, the MagNA Pure LC system (MAG; Roche) and the manual RiboPure-Blood RNA method (RIBO; Ambion); Beta glucoronidase RNA (GUS) was amplified by LightCycler PCR to evaluate the quality of both ... More
Expression profile of MicroRNAs in young stroke patients.
Authors:Tan KS, Armugam A, Sepramaniam S, Lim KY, Setyowati KD, Wang CW, Jeyaseelan K
Journal:PLoS One
PubMed ID:19888324
The methods currently available for diagnosis and prognosis of cerebral ischaemia still require further improvements. Micro-RNAs (small non-coding RNAs) have been recently reported as useful biomarkers in diseases such as cancer and diabetes. We therefore carried out microRNA (miRNA) profiling from peripheral blood to detect and identify characteristic patterns in ... More
MicroRNA expression in the blood and brain of rats subjected to transient focal ischemia by middle cerebral artery occlusion.
Authors:Jeyaseelan K, Lim KY, Armugam A
Journal:Stroke
PubMed ID:18258830
Several hundred small RNAs called microRNAs (miRNAs) have been identified and characterized from various organisms, including humans. In humans, some of these miRNAs have been found to regulate (patho)physiologic conditions such as tumor progression/regression, cholesterol and glucose homeostasis, etc. In this report, we present data on the miRNAs expressed under ... More
Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome.
Authors:Gong Q, Zhang L, Vincent GM, Horne BD, Zhou Z
Journal:Circulation
PubMed ID:17576861
Long-QT syndrome type 2 (LQT2) is caused by mutations in the human ether-a-go-go-related gene (hERG). More than 30% of the LQT2 mutations result in premature termination codons. Degradation of premature termination codon-containing mRNA transcripts by nonsense-mediated mRNA decay is increasingly recognized as a mechanism for reducing mRNA levels in a ... More
5 total citations

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