Products - DNA Microarrays - Bacterial Whole Genome Microarrays for Gene Expression and Genotyping Applications in Prokaryotic Genomics
Arrayit Bacteria Microarrays enable comprehensive genome-wide gene expression analysis of important bacterial species including Escherichia coli, Bacillus subtilis, Salmonella typhimurium and Staphylococcus aureus. Genomic microarray content is derived from complete and fully annotated bacterial genomic sequences to provide the most complete gene coverage available for these bacterial species. Bacteria Microarrays offer the highest sensitivity and specificity of any product on the market, empowered by long-mer oligonucleotides, proprietary attachment and surface chemistry, and a unique tiling design. Bacteria Microarrays allow users to rapidly and economically explore cell signalling, chemotaxis, metabolism, pathogenicity, DNA replication, transcription, translation and many other bacterial pathways. Arrayit offers a complete line of instruments, tools, kits, reagents and software to fully support Bacteria Microarrays experimentation. Complete bacterial genome gene expression services are also available.
- Quality Control
- Product Description
- Kit Contents
- Technical Notes
- Short Protocols
- Complete Protocols
- Technical Assistance
- Troubleshooting Tips
- Recommended Equipment
- Ordering Information
- Storage Conditions
The use of ArrayIt® brand products will improve the precision, speed and affordability of your microarray research in genomics, proteomics, biomedicine, pharmaceuticals and diagnostics. This handbook contains all the information required to take full advantage of Arrayit's Bacteria DNA Microarrays.
Arrayit uses the highest quality control (QC) and quality assurance (QA) measures to ensure the quality of our ArrayIt® Pathways Human DNA Microarrays. The finest science and engineering was used to develop this product. The use of advanced bioinformatics, ultra-pure oligonucleotides, superior surface chemistry and the world’s most advanced microarray cleanroom manufacturing facilities guarantees that Bacteria Microarrays outperform the highest industry standards.
Arrayit Bacteria Microarrays represent the most advanced bacteria DNA microarrays in the industry. These microarrays are designed using complete and fully annotated bacterial genome sequence using sophisticated tiling informatics and the highest gene content available. These microarrays are manufactured in state-of-the-art class 1 cleanrooms using proprietary printing technology and the strictest QC and QA procedures. All our microarrays offer quality and performance that cannot be obtained from any other microarray, PCR or next generation sequencing approach. These microarrays are compatible with all slide based microarray scanners.
Users will appreciate the following features of the Pathways Focused DNA Microarrays:
- Designed from complete and fully annotated bacterial genome sequences
- Annotated across GenBank, UniGene, GoldenPath, RefSeq and AceView
- Made using long oligonucleotide elements
- Tiled long-mer design streamlines data analysis
- Devoid of pseudogenes, and redundant and chimeric sequences
- Control sequences add precision and reliability
- Contains widely used Ambion and Stratagene controls
- Detect many bacterial mRNAs in a single hybridization reaction
- Manufactured using proprietary printing technology
- Oligonucleotides exhibit high purity levels
- Printed on atomically smooth glass substrates for improved precision
- Proprietary series 3 Arrayit glass offers world’s lowest intrinsic fluorescence
- Compatible with an installed base of >10,000 slide scanners
- Allow validation of Affymetrix, Agilent, ABI, GE, Qiagen PCR arrays and other vendors
- 75 µl reaction volume accelerates kinetics and minimizes sample consumption
- Format compatible with all standard data quantification and mining packages
- Compatible with dozens of DNA and RNA amplification and labeling schemes
- Utilize fluorescent, colorimetric and chemilluminscent detection
- One, two, three and four color detection possible
- Detect limit: 1 mRNA per 1,000,000
- Dynamic range: >1,000,000-fold
- Chip-to-chip CVs: ±20%
- Corner chamfer provides unambiguous spatial orientation
- Barcode assists in data tracking
- Sophisticated anti-static packaging improves usability
- Produced in our automated manufacturing facilities
- Microarrays are shipped ready for hybridization.
Each Bacteria Microarrays kit contains the following components:
- 1 x Genomic Bacteria Microarray
- 1 x Cover Slip (25 x 40 mm)
- 1 x Bateria Microarrays Gene List
- 1 x GAL File Quantification Spot Map
Figure 2. Arrayit Bacterial Escherichia coli, Bacillus subtilis, Salmonella typhimurium and Staphylococcus aureus microarays use the same packaging as our H25K Human Genome Microarrays. Each kit manufactured and packaged in class 1 cleanrooms and heat-sealed in anti-static packaging to ensure optimal performance and indefinate shelf life if stored clean and dry.
Figure 3. Arrayit Bacterial Microarays are manufactured in an 18 x 22 mm area (hatched) located in the horizontal center and 19 mm from the top of the 25 x 76 mm glass substrate slide. The corner chamfer and barcode are located at the top of the substrate slide as shown. The printed microarray is compliant with the TrayMix S4 Hybridization Station instruments, which react the labeled sample with the microarray in a lumen created by a gasket (double red lines).
Figure 4. Arrayit Bacterial Microarays are manufactured in an 18 x 22 mm area (green) located in the horizontal center and 19 mm from the top of the 25 x 76 mm glass substrate slide. The corner chamfer and barcode are located at the top of the substrate slide as shown. The printed microarray is compliant with cover slips (left) and automated hybridization with the TrayMix S4 (left center) and Agilent (right center) instruments. Custom microarrays (right) can be printed in an 18 x 47 mm region for compliance with many formats.
Arrayit Bacteria Microarray oligonucleotides contain sense strand information, and therefore nucleic acid probe mixtures reacted with these microarrays must contain anti-sense molecules to hybridize to the sense oligonucleotides present on the chip. The long oligonucleotide sequences present in each feature are annotated across the AceView, Entrez, RefSeq, UniGene, KnownID, and GenBank databases. Each oligonucleotide also includes a unique MicroarrayID, which identifies the sequence on microarary and allows customers to purchase the sequence by specifying the MicroarrayID. Gene descriptions are based on the best descriptions available from GenBank and AceView. GAL files and gene lists for Bacterial Whole Genome Microarrays are provided by electronic mail at firstname.lastname@example.org.
Short Protocol (Steps 1-7)
1. Prepare a labeled probe from a biological sample.
3. React the probe sample with a Bacterial Microarray to allow molecular binding.
4. Wash the Bacterial Microarray to remove unbound probe molecules.
5. Detect Bacterial Microarray signals by scanning or imaging.
6. Quantify the Bacterial Microarray signals.
7. Perform data analysis.
Complete Protocol (Steps 1-7)
1. Prepare a labeled probe from a biological sample. Bacteria Microarrays contain specific sets of long oligonucleotides representing genes in a specific Pathways in the human genome. These microarrays can be used to query a single probe mixture, or multiple probes prepared using multiple fluorescent labels in multi-color DNA and RNA hybridization. For gene expression applications, each oligonucleotide designed to be complimentary to the 3’ end of a gene and is optimized to hybridize to as many transcripts as possible in cases where genes express multiple mRNAs. Each spot will detect a majority of transcripts for every gene on the microarray single reaction. There are three fundamental principles that should be used for sample preparation: (1) Sample integrity must be high. DNA, mRNA and protein molecules must be full length and free of contaminating enzymes that can produce nucleic acid and protein degradation. (2) Probe labeling must be efficient. Probes should be checked prior to reactions with to ensure that the probe mixtures are highly fluorescent. The most common cause of poor performance is poor sample/probe preparation. (3) Probe mixtures must be pure. Prior to hybridization, probe mixtures should be purified to remove non-incorporated dyes and other contaminants that can increase background noise. This step is well worth the small investment in time and money, as it will greatly increase performance. Direct and indirect fluorescent and non-fluorescent labeling techniques have been described extensively in the literature and a host of commercial labeling kits are available from many different vendors. Arrayit offers an extensive line of purification, amplification and labeling kits for DNA, mRNA and protein labeling applications. For gene expression applications, Arrayit’s Micro-Total RNA Extraction Kit, MiniAmp Bacterial mRNA Amplification Kit, Indirect Amino Allyl Fluorescent Labeling Kit, and Universal Reference mRNA are highly recommended for maximum signal strength.
2. React the probe sample with microarray to allow molecular binding. The microarray on the chip is located 10mm down from the top printed on the same side as the barcode of glass substrate. For additional help with side orientation, the 1.4 mm cropped corner of the glass substrate (“chamfer”) should be located in the upper right corner of the glass substrate when the barcode is facing upward. Powder free nitrile gloves should be worn at all time while handling microarrays to avoid the transfer of dust, debris, hand oils, and other contaminants that can interfere with hybridization and detection. ArrayIt® Microarray Cleanroom Gloves provide superior hand protection for microarray applications. The recommended probe sample volume for Bacteria Microarrays is 50 µl, which will form a 60 µm sample layer on the microarray when using a 25 x 40 mm lifter type cover slip. The recommended hybridization buffer is HybIt® 2 Hybridization Solution. Arrayit provides an affordable and widely used line of Hybridization Cassettes and these work very well for low to medium throughput applications. Users may also employ the Arrayit TrayMix S4 Automated Hybridization Stations to allow automated reactions and washing. Probe mixtures can be generated from cloned or cellular DNA, RNA or protein, and dozens of fluorescent and non-fluorescent labeling schemes have been described in the literature. For gene expression applications with Bacteria Microarrays use 0.5 µg of amino-allyl labeled cDNA per color (1.0 µg total of green and red probe for two-color experiments) is recommended to produce strong hybridization signals. Probe mixtures should be spun at 18,000 x g for 1 min to pellet debris prior to use. The microarray substrate slide, hybridization cassette or chamber, lifter slip and probe mixture should be pre-heated to 42°C for 5 min prior to hybridization to ensure low and uniform background. Pipette the 50 µl probe mixture directly onto the center of the microarray and quickly place the lifter slip onto the probe droplet, allowing the probe mixture to sheet evenly across the surface. Probe mixtures should be reacted for 3.5 hours at 42°C for gene expression applications, though different times and temperatures can be used for probe mixtures of different concentration and complexity. Probes derived from cloned and recombinant sources will probably produce satisfactory results within 5-10 minutes because the molecular complexity of such sources is low and Bacteria Microarrays performance is extremely high. Probe mixtures derived from complex sources such as human genomic DNA, mRNA and protein may require more than 3.5 hours to produce strong signals. In rare cases, users may opt for up to 18 hour reaction times, though probe drying and elevated background noise can become an issue with prolonged hybridizations. After the hybridization step is complete, users should proceed quickly to the wash steps to prevent probe drying and elevated background.
3. Wash microarrays to remove unbound probe molecules. After the probe binding reaction is complete, the microarray must be washed to remove unbound material. Oligonucleotide-DNA or oligonucleotide-RNA hybrids are typically washed at high-stringency to remove labeled probe molecules that have bound weakly or non-specifically. Lesser stringency can be use in cases where DNA and mRNA probe mixtures are derived from homologous species such as primate, mouse and rat. For protein binding applications, oligonucleotide-protein complexes should be washed to remove proteins that have bound weakly or non-specifically. The oligonucleotides on Bacteria Microarrays are bound covalently to the glass substrate, and therefore the oligonucleotides themselves are stable to elevated temperature (≤70°C), low salt, and other neutral pH (pH 6-8) treatments. Users should avoid extremes in temperature and pH to avoid damaging the oligonucleotides. Protein experiments with bacteria microarrays typically make use of reactions 20-37°C and washes with phosphate-buffered saline (PBS) buffers containing dilute additions of detergent (e.g. 0.1-0.01% TritonX100). Prior to washing, the lifter slip must be removed from the microarray surface to allow efficient washing and to avoid scratching the spots on the surface. For gene expression applications, quickly remove the lifter slip by submerging microarray for 5-10 sec in 42°C in Wash Buffer A and wash as follows: 5 min at 42°C in Wash Buffer A, 5 min at room temperature in Wash Buffer B, and 1 min at room temperature in Wash Buffer C, followed by a 1 sec dunk in dH2O. Washes should be performed in High-Throughput Wash Stations with moderate mixing or in the TrayMix S4 Hybridization Station. Users can experiment with different wash buffers and different temperatures (20-65°C) to optimize the washing process for a particular application. Following the final wash step, microarrays should be dried quickly by centrifugation for 3 sec in an Arrayit Microarray High-Speed Centrifuge in preparation for scanning.
4. Detect signals by scanning or imaging. Bacteria Microarrays should be inserted into a microarray scanning or imaging device to acquire the signals. The Arrayit InnoScan® 710 and 900 Fluorescence Scanners and the highly affordable Arrayit SpotLight Microarray Fluorescence Scanner works well for this application, though all Bacteria Microarrays are compatible with all major brands of microarray glass microscope slide microarray scanners. Scanners and imagers should be capable of at least 10 µm resolution, the lowest recommended resolution setting. Scanning at 3-5 µm resolution produces higher quality images. The selected scan area should be large enough to capature all spots in a single image. In addition to the resolution and scan area settings, correct settings should be used for wavelength(s), gain, laser intensity, PMT, and other technical parameters required to produce high quality, data-rich images. For expression analysis applications involving complex mixtures of mRNA varying greatly in concentration, multiple scanner settings (e.g. low and high sensitivity) across two or more images can be used to capture signals spanning up to 6 orders of magnitude. Multi-color experimentation involving, for example, cyanine 3 and cyanine 5 labels, obviously require data capture at two different wavelengths (e.g. 532 and 635 nm). Images should be saved as 16-bit TIFF files for quantification and downstream analysis.
5. Quantify the signals. Arrayit MAPIX® ande ImageGene quantification software is highly recommended for quantification. Use GAL file spot map provided with the microarrays. Place grid over the file, making sure that all subgrids and spots are properly aligned. MAPIX® quantification settings should be set to allow the software to find all of the printed spots in an automated manner. The following settings work well for most applications: Max position offset (% pitch) 30, Min. diameter
(% Dth) 80, Max. diameter (% Dth) 190, S/B border width (pixels) 1.6 and Background diameter (pitch) 1.6. Once the grid has been accurately aligned, the quantification process should be initiated to extract data values from H25K using the photmetric calculation command. The extracted data should be saved and then opened in Microsoft Excel or some other software program for downstream analysis.
6. Perform data analysis. Properly quantified images will yield great data. Values should be analyzed using a variety of inclusion and exclusion criteria to ensure statistical relevance of all values. For most applications, background-subtracted median signal intensities provide the most accurate reporting of spot signal intensity. Data from multiple images can be compared to identify up- and down-regulated genes in expression profiling experiments. Arrayit offers highly sophisticated Genome Pathways Builder software analysis for Biomarker Discovery and Validation Services customers. Genome Pathways Builder constructs biological Pathwayss from vast quantities of expression data, providing customers with a detailed molecular understanding of a disease process. Genome Pathways Builder also allows pharmaceutical clients to understand the mode of drug action as well as off-targets as a means of benchmarking pharmaceutical leads prior to and during clinical trials.
Please contact us if you have any questions, comments, suggestions, or if you need technical assistance. By electronic mail, use email@example.com and type "Bacterial Microarrays technical assistance" into the subject line. By telephone, call (408) 744-1331 between the hours of 8AM and 7PM PST Monday through Friday. We want to hear about your successes and are always happy to publish contributed Bacterial Microarray sample data on our website.
1. Weak signals
- Degraded DNA, RNA or protein. Check sample integrity.
- Poor sample labeling efficiency. Check probe mixture.
- Wash stringency too high.
2. High background fluorescence
- Probe mixture drying out during hybridization. Keep hydrated for duration.
- Probe drying after hybridization. Transfer quickly to wash steps.
- Probe volume too low. Use 75.0 µl for bacterial microarrays.
- Purify probe mixture to remove contaminating unincorporated fluors.
- Hybridization time too long. Use a maximum time of 6 hrs.
- Poor washing procedure. Increase time or stringency.
3. Low frequency of differentially expressed genes (gene expression)
- Wash stringency too low. Reduce salt and/or increase temperature.
- Messenger RNA samples highly similar. Check samples/stimuli.
4. Artifacts observed in two-color experiments (gene expression)
- Dye effects to blame. Swap colors and re-examine data.
To order Arrayit Brand Products: call 408-744-1331, fax 408-744-1711, email firstname.lastname@example.org, or click on the purchase buttons above to proceed directly to the purchase pages.
Price (U.S. Dollars)*
Escherichia coli K12 Whole Genome Microarrays
Arrayit Escherichia coli K12 Whole Genome Microarrays contain long-mer oligonucleotides representing 99.1% of the 4,331 genes present in the E. coli genome. The tiled 12,185 oligonucleotides allow analysis of 4,294 genes and each of the 12,185 elements are present in triplicate in the 40K format. Arrayit 40K E. coli chips utilize the standard 25 x 76 mm glass substrate slide format, which is fully supported by Arrayit's entire line of microarray scanners, hybridization stations, tools, kits and reagents. Pricing is per microarray.
Bacillus subtilis Whole Genome Microarrays
Arrayit Bacillus subtilis subsp. subtilis str. 168 Whole Genome Microarrays contain long-mer oligonucleotides representing 99.2% of the 4,106 genes present in the B. subtilis genome. The tiled 11,495 oligonucleotides allow analysis of 4,073 genes and each of the 11,495 elements are present in triplicate in the 40K format. Arrayit 40K B. subtilis chips utilize the standard 25 x 76 mm glass substrate slide format, which is fully supported by Arrayit's entire line of microarray scanners, hybridization stations, tools, kits and reagents. Pricing is per microarray.
Proteus mirabilis Whole Genome Microarrays
Arrayit offers Proteus mirabilis Whole Genome Microarrays containing long-mer oligonucleotides representing >98.6% of the 3,740 genes present in the Proteus mirabilis genome. Proteus mirabilis microarrays contain 10,413 oligonucleotides, which allow a survey of 3,686 or 98.6% of the genes present in the Proteus mirabilis genome. Each of the 10,413 oligonucleotides are present in triplicate on the 40K format. Arrayit 40K Proteus mirabilis chips utilize the standard 25 x 76 mm glass substrate slide format, which is fully supported by Arrayit's entire line of microarray scanners, hybridization stations, tools, kits and reagents. Pricing is per microarray.
Staphylococcus aureus MRSA252 Whole Genome Microarrays
Arrayit Staphylococcus aureus subsp. aureus MRSA252 30K Oligonucleotide Microarrays contain long-mer oligonucleotides representing 98% of the 2,744 genes present in the Staphylococcus aureus genome. Staphylococcus aureus microarrays contain 7,459 oligonucleotides replicated 4 times on the microarray for a total of 29,836 oligonucleotide elements in the 30K format, fully compatible with cover slip, TrayMix S4 and Agilent hybridization stations. Arrayit 30K S. aureus microarrays utilize the standard 25 x 76 mm glass substrate slide format, which is fully supported by Arrayit's entire line of microarray scanners, tools, kits and reagents. Pricing is per microarray.
Salmonella typhimurium str LT2 Whole Genome Microarrays
Arrayit Salmonella enterica subsp. enterica serovar typhimurium str LT2 30K Oligonucleotide Microarrays contain long-mer oligonucleotides representing 95% of the 4,525 genes present in the Salmonella typhimurium genome. Salmonella typhimurium microarrays contain more than 4,266 oligonucleotides replicated 6 times on the microarray for a total of more than 25,000 oligonucleotide elements in the 30K format, fully compatible with cover slip, TrayMix S4 and Agilent hybridization stations. Arrayit 30K S. typhimurium microarrays utilize the standard 25 x 76 mm glass substrate slide format, which is fully supported by Arrayit's entire line of microarray scanners, tools, kits and reagents. Pricing is per microarray.
*International pricing may vary as much as 30% (or more depending on country) due to import duties, stocking fees and technical support.
*Add shipping and handling to all orders.
Arrayit DNA Microarrays are manufactured, processed and packaged in advanced class 1 cleanroom facilities and are stable at room temperature (25°C) for 6 months from the date of receipt. Unprocessed microarays from Arrayit have an indefinate shelf life. If you wish to receive your microarrays unprocessed please specify this at the time of ordering. Store in the sealed anti-static shipping envelope and avoid exposure to elevated temperature, humidity, and dust until use.
Arrayit DNA Microarrays are scientifically developed and manufactured in advanced class 1 cleanrooms. They are sold for research purposes only and is not for use in human diagnostics or for drug purposes, and should not be administered to humans in any way. Extreme care and exact attention should be practiced in the use of the materials described herein. All Arrayit products are subject to extensive quality control and are guaranteed to perform as described when used properly. Any problems with these products should be reported to Arrayit immediately. Our liability is limited to the replacement of the product. Any misuse of this product is the full responsibility of the user, and Arrayit makes no warranty or guarantee under such circumstances.
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