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Services - eChips Custom Microarray Services from TeleChem International, Inc. provide unprecedented access to the microarray revolution at an unbeatable price. By uniting the power of microarray technology with the universality of the Internet, TeleChem makes microarrays affordable, versatile and easy to use. Every microarray is manufactured in one of our state-of-the-art class 100 cleanroom facilities, with the most advanced robotics, surfaces and coupling chemistries in the industry. Our particle- and ribonuclease-free manufacturing laboratories provide microarrays of dazzling quality. eChips allow customers to mine existing databases for sequences of interest and send them by electronic mail for microarraying. Synthesized oligonucleotides and peptides are printed on optically flat SuperAmine or SuperAldehyde substrates. eChips allow researchers to create a nearly infinite variety of microarrays for basic research, clinical, pharmaceutical and agricultural applications. Because the customer performs all of the steps downstream of manufacturing, the data remain completely confidential. Imagine any nucleic acid or peptide molecule, from any organism, for any application on a pristine surface and you are beginning to understand the breadth and depth of our Custom Microarray Services. TeleChem International, Inc. eChips set a new standard in microarray technology.Please send requests for quotes by electronic mail to arrayit@arrayit.com. Table of Contents
Introduction Quality Control and Use Description of Services eChips: Customer provides information for up to 9,600 sequences
Technical Assistance Short Protocols |
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Table 1. Synthetic sequences for eChips. |
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Design Note Complete Protocols 2. Send a Purchase Order number, referencing your quote number to: TeleChem International, 524 East Weddell Drive, Sunnyvale, CA 94089. Phone: (408) 744-1331, Fax (408) 744-1711 or by email to arrayit@arrayit.com. 3. Send sequences by electronic mail as Excel or tab delimited text file. Send the Excel spreadsheet or tab delimited text file as an attachment to an email that identifies the order and has complete contact information. Please remember that due to a high volume of orders, all electronic mail communications must contain complete contact information, including name, affiliation, telephone number and FAX number. Failure to provide these details may delay your order. Your oligo sequences or genomic information for oligo design can also be sent to us by overnight mail in an Excel spreadsheet or tab delimited file format a 3.5 inch floppy disks or Zip disks (PC formatted) at the address above. Please include a letter or email that references your quote number and has complete contact information. 4. Wait 2-6 weeks depending on details of your order. Once your order is placed, we will provide a more exact timeline. The time to process orders depends on the volume of orders in the queue and on the size of your order. TeleChem International, Inc. will make every attempt to process your order as quickly as possible. 5. Obtain eChips shipped directly to you by Express Mail or by the shipping method that you specify. All eChips will arrive complete with barcodes and corner chamfer. The barcode contains an identifying number that is unique to each chip in your order. The corner chamfer is provided to allow the user to determine easily which side of the substrate contains the printed microarray and defines the top of the substrate. The printed microarray is located on the same side of the substrate as the barcode. The corner chamfer should appear in the upper right corner if the barcode is at the bottom of the substrate. You will also receive a content file that shows the location of each printed target sequence on the microarray substrate. 6. Process the eChips to remove unbound target sequences. Processing protocols vary according to the Substrate used and the target sequences. Detailed protocols are available electronically on the SuperAmine and SuperAldehyde product page. 7. Label and purify probes. There are a myriad of enzymatic and synthetic methods used to label probes derived from RNA, oligonucleotides and proteins. Samples can be labeled using direct labeling whereby fluorescent tags are incorporated into the molecules in the sample. Alternatively, samples can be labeled by indirect means prior to hybridization such that epitopes such as biotin or amino allyl are incorporated into the sample, then the molecules are made fluorescent using fluorescently labeled streptavidin or reactive fluorescent dyes. Post hybridization detection can also be achieved using secondary labeling molecules such as dendrimers (Genisphere, Inc) or antibody-containing fluorescent molecules. Samples can be nucleic acids, proteins or other types of molecules. Users should select the labeling procedure that works best for their application. Labeling procedures and tips are available under DNA Microarray Protocols, Super Microarray Substrates, Hybridization Products, and Fluorescent Probe Purification. An electronic library containing nearly 1,000 publications provide a wealth of information on labeling and purification procedures. Our specialists are happy to provide advice and feedback on probe labeling and purification. 8. Perform a hybridization or biochemical reaction. Probes should be reacted with the processed eChips to allow the molecules to interact with their cognate targets on the chip. This step is best accomplished by reacting the sample to the processed microarray underneath a cover slip positioned over the microarray. The cover slip should extend ~2 mm beyond the edges of the microarray on all sides to ensure that the sample covers all the spots. Sample volumes are typically ~2.0 µl per cm2, such that total reaction volumes of 3.0 µl and 20 µl work well for the 12 mm x 12 mm and 22 mm x 40 mm cover slips, respectively. The corner chamfer should be at the upper right side of the substrate relative to the user when the microarray is held vertically (with the barcode at the bottom). Buffers suitable for nucleic acid hybridizations include 5X SSC + 0.2% SDS, 1X UniHyb and 1X HybIt®. Other types of buffers such as those containing SSC, SSPE, SDS, and TritonX-100 have also been used successfully. Sample is best added to the microarray by placing the drop at the edge of the cover slip and allowing the sample to spread out between the microarray and the cover slip by capillary action. Once the sample is added, immediately place the microarray in an enclosed chamber such as a Hybridization Cassette and bring the reaction up to temperature as quickly as possible. It is critical to prevent desiccation during the biochemical reactions, as drying is the major source of elevated background fluorescence in microarray experiments. Desiccation is prevented by adding 5-25 µl of buffer to the reaction chamber. Reaction temperatures are typically 37-65°C, though different experiments may require higher or lower reaction temperatures. Reaction times are usually 2-12 hours. Information on hybridization reactions can be obtained under Hybridization Products, Super Microarray Substrates, and DNA Microarray Protocols. Our specialists are happy to provide advice and feedback on hybridization, protein, and other types of biochemical reactions involving eChips. 9. Wash eChips to remove unbound probe molecules. Once the eChips are reacted with labeled probe samples, the chips must be washed to remove unbound molecules. Following the biochemical reaction, unbound sample should be washed off the surface. For cDNA hybridizations, the following protocol works well. Remove the microarray from the Hybridization Cassettes and place it in a High-Throughput Wash Station and wash according to the protocols provided with the Microarray Wash Buffers. Wash conditions should be modified for different types of reactions and different applications. Make sure the cover slip falls off within 1 minute after transfer into the wash buffer. Wash buffers pre-heated to 42°C can be used to speed the release of the cover slip from the microarray. Failure to remove the cover slip within 1 minute after transfer to the wash buffer may lead to elevated background fluorescence. There are numerous washing protocols available and details are available under DNA Microarray Protocols, Super Microarray Substrates, Hybridization Products, and Microarray Wash Buffers. An electronic library containing nearly 1,000 publications provide a wealth of information on microarray wash procedures. Spin the substrates dry by centrifugation for 10 seconds in a Microarray High-Speed Centrifuge. Our specialists are happy to provide advice and feedback on eChip washing strategies. 10. Detect the fluorescent signals. Once the eChips are reacted and/or stained, and washed, the fluorescent signals must be detected. Detection is best performed using one of the high-quality commercial instruments available. Commercial systems are available from PE (Packard Bioscience), Axon, Applied Precision and several other vendors. Detection should be performed such that the most intense signals on the microarray produce sub-saturating values. Rare species in the probe mixture can be quantified using instrument settings that maximize detectivity. Adjusting the laser power, PMT gain, capture time and other parameters provide enormous detectivity in microarray assays. 11. Quantify and model the data. Data quantification and mining can be performed using a variety of custom and commercial software packages. Tips for Design and Use |
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Product Contents Our eChip services are divided into three stages, Oligo Design, Oligo synthesis and Custom Microarray Printing. Oligo Design Oligo Design services are available at a cost of $10 per oligo. Our oligos are designed using our TeleChem Oligo Design Directive. This Directive ensures that the oligos:
Oligo design services can take 1-2 weeks depending on the number of oligos required. Alternatively, you can design your own oligos using Array Designer Software from Premier Biosoft. Oligo Synthesis Custom Microarray Printing Scientific Publications Recommended Equipment and Reagents Ordering Information |
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