Promega

PowerPlex 18D System, 800 rxn

Varenummer: DC1808
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Note: Starting May 2016, the PowerPlex 18D System will contain WEN ILS 500 as the Internal Lane Standard, replacing CC5 ILS 500. Please visit www.promega.com/products/genetic-identity/str-amplification/wen-matrix-standards-faq/ for additional details. The PowerPlex 18D System is a multiplex STR system for use in database and paternity testing. This system is optimized for direct amplification of samples on FTA cards. This five-color multiplex allows co-amplification of the 13 CODIS loci (D18S51, D21S11, TH01, D3S1358, FGA, TPOX, D8S1179, vWA, CSF1PO, D16S539, D7S820, D13S317, D5S818) plus Amelogenin, Penta E, Penta D, D2S1338 and D19S433. All eighteen loci are amplified simultaneously in a single tube and analyzed in a single injection. The PowerPlex 18D System is compatible with ABI PRISM 3100 and 3100-Avant Genetic Analyzers and Applied Biosystems 3130, 3130xl, 3500 and 3500xL Genetic Analyzers. The PowerPlex 18D System was given NDIS approval in July 2011 for NDIS CODIS databasing.|
Eliminate DNA Extraction: Simplify and shorten sample processing with direct amplification from FTA(R), cards.Reduce PCR Time: Amplify in less than 1.5 hours using rapid cycling technology.Upload More Markers: Type D2S1338, D19S433, Penta D, Penta E, Amelogenin and the 13 CODIS loci with one kit.Automatically Assign Genotypes: Panels and bins text files are required for automatic assignment of genotypes using the GeneMapper(R), ID and ID-X software and are available for download.

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Store kit at -20°C. Upon receipt, move 2800M Control DNA and WEN ILS 500 to 4°C storage.|U.S. Pat. Nos. 5,843,660, 6,479,235, 6,221,598 and 7,008,771, Australian Pat. No. 724531, Canadian Pat. Nos. 2,118,048 and 2,251,793 and other patents and patents pending. U.S. Pat. No. 6,238,863 and other patents and patents pending. U.S. Pat. No. 6,242,235, Australian Pat. No. 761757, Canadian Pat. No. 2,335,153 and other patents and patents pending. Allele sequences for one or more of the loci vWA, FGA, D8S1179, D21S11 and D18S51 in allelic ladder mixtures is licensed under U.S. Pat. Nos. 7,087,380, 7,645,580, Australia Pat. No. 2003200444 and corresponding patent claims outside the US. STR loci are the subject of U.S. Pat. No. RE 37,984, German Pat. No. DE 38 34 636 C2 and other patents issued to the Max-Planck-Gesellschaft zur Förderung der Wissenschaften, e.V., Germany.Licensed under U.S. Pat. No. 5,587,287 and corresponding patents in other countries. For Research Use Only. Not for use in diagnostic procedures. This product or portions thereof is manufactured and sold under license from GE Healthcare under Australia Pat. No. 692230, Austria Pat. No. E236994, Belgium Pat. No. 0743987, Canada Pat. No. 2231475, EP Pat. Nos. 0743987 and 0851867, France Pat. Nos. 0743987 and 0851867, Germany Pat. Nos. 19581489, 69530286.8 and 0851867, Italy Pat. Nos. 0743987 and 0851867, Japan Pat. No. 3066984, Liechtenstein Pat. Nos. 0743987 and 0851867, Netherlands Pat. Nos. 0743987 and 0851867, Spain Pat. Nos. 2197193 and 2173310, Sweden Pat. Nos. 0743987 and 0851867, Switzerland Pat. Nos. 0743987 and 0851867, United Kingdom Pat. Nos. 0743987 and 0851867, U.S. Pat. Nos. 5,654,419, 5,688,648, 5,869,255, 6,177,247, 5,707,804, 6,028,190, 6,544,744, 7,015 000 and 5,728,528 and other pending and foreign patent applications. End User Terms and Conditions Acceptance. These terms and conditions shall govern the purchase, use, transfer and acceptance of the products described in the purchase order, quotation or invoice, which products are sold and distributed by Promega to the buyer/transferee of such products (the "End User"). The transfer/sale of products to the End User is expressly conditional upon End User's acceptance of these terms and conditions. Restrictions on Use. End Users are specifically not authorized to and are forbidden from reselling, transferring or distributing any products either as a stand alone product or as a component of another product. The right to use the products does not, in and of itself, include or carry any right of the End User to any GE Healthcare Bio-Sciences Corp.'s technology or intellectual property other than expressly provided herein. End Users may not use sequence(s) in an attempt to reverse engineer parameters of any of GE Healthcare Bio-Sciences Corp. proprietary products or services. Disclaimer of Warranties. GE Healthcare Bio-Sciences Corp. provides no warranties to end user (statutory or implied), including without limitation, as to product quality, condition, description, merchantability or fitness for a particular purpose, and all such warranties are hereby expressly disclaimed. GE Healthcare Bio-Sciences Corp. hereby expressly disclaims any warranty regarding results obtained through the use of the products, including without limitation any claim of inaccurate, invalid or incomplete results. Exclusion of Liability. GE Healthcare Bio-Sciences Corp. and its affiliates shall have no liability to an End User, including, without limitation, for any loss of use or profits, business interruption or any consequential, incidental, special or other indirect damages of any kind, regardless of how caused and regardless of whether an action in contract, tort, strict product liability or otherwise.TMR-ET, CXR-ET and CC5 dyes are proprietary.

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Monica Laukas 404 40 960 monica.laukas@nmas.no

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