MICROBExpress™ Bacterial mRNA Enrichment Kit
MICROB<i>Express</i>&trade; Bacterial mRNA Enrichment Kit
Invitrogen™

MICROBExpress™ Bacterial mRNA Enrichment Kit

The MICROBExpress™ Bacterial mRNA Enrichment Kit is for the purification of bacterial mRNA by removing rRNA from total RNA. SufficientRead more
Promo ImagePromotion
Promo code:P5906365
Don't miss out: buy 3, only pay for 2
Promo ImagePromotion
Promo code:RPUZZ25
Stock up on essentials to piece your discovery together
Have Questions?
Catalog NumberQuantity
AM1905Promo Image20 preps
Catalog number AM1905
Price (USD)
756.00
Each
In stock
Add to cart
Quantity:
20 preps
Recurring order eligible. Learn more »
Price (USD)
756.00
Each
Add to cart
Ask our AI about this Product
The MICROBExpress™ Bacterial mRNA Enrichment Kit is for the purification of bacterial mRNA by removing rRNA from total RNA. Sufficient reagents for 20 mRNA purifications, each from 10 μg of total RNA are provided. Features of the MICROBExpress Kit:

• Dramatically increase the sensitivity of array analyses and other procedures
• Removes >95% of 16S and 23S rRNA from bacterial RNA
• Simple procedure takes less than 2 hours
• Works with many Gram positive and Gram negative bacteria

Rapid purification of bacterial mRNA
Isolating mRNA from bacteria has been virtually impossible, until now. The MICROBExpress Kit uses a novel technology to remove >95% of the 16S and 23S rRNA from total RNA of E. coli and other bacterial species. The kit is suitable for mRNA purification from a broad spectrum of Gram positive and Gram negative bacteria. The mRNA isolated with the MICROBExpress Kit is a superior template for synthesizing labeled cDNA for array analysis, and is ideal for quantitative RT-PCR, northern applications, and cDNA library construction. Efficient removal of 16S and 23S rRNA from bacterial RNA dramatically increases sensitivity in downstream procedures (see figure).

Start with any total RNA sample
This host-bacterial cell total RNA mixture can be obtained by a variety of RNA isolation methods. The MICROBExpressKit specifically removes rRNAs; small RNAs (i.e., tRNA and 5S rRNA) are not removed. Using total RNA that lacks small RNAs as the starting material for MICROBExpressKit produces the highest possible level of mRNA enrichment (see accessory products). In the first step of the MICROBExpress Kit procedure, total RNA is mixed with an optimized set of capture oligonucleotides that bind to the bacterial 16S and 23S rRNAs. Next, the rRNA hybrids are removed from the solution using derivatized magnetic microbeads. The mRNA remains in the supernatant and is recovered by ethanol precipitation.

Accessory products
A magnetic stand is required for use this kit. They are available in several formats, including the Single Place Magnetic Stand (Cat. No. AM10026), 6 Tube Magnetic Stand (Cat. No. AM10055), and 96-well Magnetic Stands (Cat. Nos. AM10027 and AM10050). The RiboPure™-Bacteria Kit (Cat. No. AM1925) is ideal for the purification of total RNA lacking small RNAs. Small RNAs can be removed from total RNA using the MEGAclear™ Kit (Cat. No. AM1908).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Final Product TypemRNA (Bacterial)
For Use With (Application)Microarray Analysis, Reverse Transcriptase PCR (RT-PCR), cDNA Library Construction, Northern Blotting
High-throughput CompatibilityNot High-throughput Compatible (Manual)
No. of Reactions20 Preps
Product LineAmbion™, MICROBEnrich
Quantity20 preps
Isolation TechnologyHybridization Capture, Magnetic Bead
Sample TypeTotal RNA (Bacterial)
TargetTotal RNA
Unit SizeEach
Contents & Storage
Store Control RNA, Capture Oligo Mix, Glycogen, and 3M Sodium Acetate at -20°C.

Store Oligo MagBeads, Binding Buffer, and Wash Solution at 4°C

Store Nuclease-free Water, 1.5mL tubes, and Collection tubes at room temperature.
Have questions about this product? Ask our AI assisted search.
This is an AI-powered search and may not always get things right. You can help us make it better with a thumbs up or down on individual answers or by selecting the “Give feedback" button. Your search history and customer login information may be retained by Thermo Fisher and processed in accordance with our Privacy Notice.

Figures

Customers who viewed this item also viewed



Documents & Downloads

Certificates

Lot #Certificate TypeDateCatalog Number(s)
2740724Certificate of AnalysisJun 12, 2023AM1905
2740709Certificate of AnalysisJun 12, 2023AM1905
2712965Certificate of AnalysisApr 29, 2023AM1905
2712959Certificate of AnalysisApr 29, 2023AM1905
2712416Certificate of AnalysisApr 29, 2023AM1905
5 results displayed, search above for a specific certificate

Safety Data Sheets

Citations & References (5)

Citations & References
Abstract
Structure and complexity of a bacterial transcriptome.
Authors:Passalacqua KD, Varadarajan A, Ondov BD, Okou DT, Zwick ME, Bergman NH
Journal:J Bacteriol
PubMed ID:19304856
'Although gene expression has been studied in bacteria for decades, many aspects of the bacterial transcriptome remain poorly understood. Transcript structure, operon linkages, and information on absolute abundance all provide valuable insights into gene function and regulation, but none has ever been determined on a genome-wide scale for any bacterium. ... More
Identification of new genes in Sinorhizobium meliloti using the Genome Sequencer FLX system.
Authors:Mao C, Evans C, Jensen RV, Sobral BW
Journal:BMC Microbiol
PubMed ID:18454850
Sinorhizobium meliloti is an agriculturally important model symbiont. There is an ongoing need to update and improve its genome annotation. In this study, we used a high-throughput pyrosequencing approach to sequence the transcriptome of S. meliloti, and search for new bacterial genes missed in the previous genome annotation. This is ... More
Validation of two ribosomal RNA removal methods for microbial metatranscriptomics.
Authors:He S, Wurtzel O, Singh K, Froula JL, Yilmaz S, Tringe SG, Wang Z, Chen F, Lindquist EA, Sorek R, Hugenholtz P
Journal:Nat Methods
PubMed ID:20852648
The predominance of rRNAs in the transcriptome is a major technical challenge in sequence-based analysis of cDNAs from microbial isolates and communities. Several approaches have been applied to deplete rRNAs from (meta)transcriptomes, but no systematic investigation of potential biases introduced by any of these approaches has been reported. Here we ... More
Transcriptome analysis of a phenol-producing Pseudomonas putida S12 construct: genetic and physiological basis for improved production.
Authors:Wierckx NJ, Ballerstedt H, de Bont JA, de Winde JH, Ruijssenaars HJ, Wery J
Journal:J Bacteriol
PubMed ID:17993537
The unknown genetic basis for improved phenol production by a recombinant Pseudomonas putida S12 derivative bearing the tpl (tyrosine-phenol lyase) gene was investigated via comparative transcriptomics, nucleotide sequence analysis, and targeted gene disruption. We show upregulation of tyrosine biosynthetic genes and possibly decreased biosynthesis of tryptophan caused by a mutation ... More
Profiling Caenorhabditis elegans non-coding RNA expression with a combined microarray.
Authors:He H, Cai L, Skogerbø G, Deng W, Liu T, Zhu X, Wang Y, Jia D, Zhang Z, Tao Y, Zeng H, Aftab MN, Cui Y, Liu G, Chen R
Journal:Nucleic Acids Res
PubMed ID:16738136
Small non-coding RNAs (ncRNAs) are encoded by genes that function at the RNA level, and several hundred ncRNAs have been identified in various organisms. Here we describe an analysis of the small non-coding transcriptome of Caenorhabditis elegans, microRNAs excepted. As a substantial fraction of the ncRNAs is located in introns ... More
5 total citations

Other products to consider



Share catalog number, name or link

1x1 image pixel for data collection