DyeEx Kits

For removal of unincorporated dye terminators from 1–24 or 1–96 sequencing reactions

Features

  • Fast procedure with only two short centrifugation steps
  • Ready-to-use prehydrated gel-filtration material
  • Efficient removal of any dye terminator
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DyeEx 96 Kit (4)

Cat. No. / ID: 63181

4 DyeEx 96 Plates; 4 Collection Plates, 48-Well
£336.00
Kit
DyeEx Kit
DyeEx 2.0 Kit
Preparations
4 x 96
24 x 96
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DyeEx Kits are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

✓ 24/7 automatic processing of online orders

✓ Knowledgeable and professional Product & Technical Support

✓ Fast and reliable (re)-ordering

Product Details

DyeEx Kits provide either spin columns or 96-well plates and use gel-filtration technology to remove dye terminators from sequencing reactions, including reactions for Sanger sequencing. Sequencing reactions are loaded onto the pre-hydrated gel-filtration material. After a short centrifugation step, the reactions are ready to be loaded onto a capillary sequencer. Unincorporated dye terminators are retained in the gel matrix.

Performance

DyeEx Kits remove any type of dye terminator from 10–20 µl sequencing reactions including BigDye, dRhodamine dye, Rhodamine, DYEnamic ET and WellRED terminators. After cleanup, the sequencing reactions can be separated on any capillary sequencer. We recommend the DyeEx 96 Kit using the optimized protocol.


High-quality sequencing


DyeEx Kits are optimized for fast and convenient dye-terminator removal leading to high-quality sequencing results. In contrast, sequencing-reaction cleanup by ethanol precipitation is very time consuming (see table "Comparison of DyeEx procedure and ethanol precipitation") and inefficient. The failure to remove dye terminators efficiently often leads to the appearance of dye blobs in sequencing data making stretches of sequence unreadable. Using DyeEx Kits for sequencing reaction cleanup ensures that the reactions loaded onto sequencing instruments are free of dye terminators. Without dye blobs, the sequence is easily readable throughout (see figure  "Superior sequencing results"). Signal intensities are high, resulting in long read lengths (see figure  "Long-read sequence").

Comparison of DyeEx procedure and ethanol precipitation

Procedure DyeEx 2.0 Spin DyeEx 96 Ethanol
precipitation
Time required*
(12 samples, spin format)
10 minutes N.A. >45 minutes
Time required*†
(Microplate format for 96 samples)
N.A. 18 minutes >60 minutes
Handling Ready-to-use
spin format
Ready-to-use Multiple
pipetting steps
Sequence quality ++ ++ +

N.A.: not applicable

* Does not include time required to dry down samples before gel loading (where applicable).
† Using the standard protocol.

See figures

Principle

The DyeEx procedure uses gel filtration to quickly and efficiently remove unincorporated terminators from sequencing reactions. Removal of dye terminators is important to prevent the unincorporated dye terminators from interfering with analysis of sequencing results. The DyeEx gel-filtration material consists of spheres with uniform pores and separates molecules according to molecular weight. When sequencing reaction mixtures are applied to DyeEx columns, dye terminators diffuse into the pores and are retained in the gel-filtration material, while labeled DNA fragments are excluded and recovered in the flow-through (see figure  "DyeEx separation principle").

See figures

Procedure

Dye-terminator removal with DyeEx Kits is fast because the procedure is so simple (see flowcharts  "DyeEx 2.0 Spin procedure" and  ”DyeEx 96 Kit procedure”). A quick centrifugation step removes storage buffer from the columns or wells, the sequencing samples are loaded and a second centrifugation step removes unincorporated dye terminators. Samples are then ready for direct loading onto a capillary sequencer or can be dried, redissolved and loaded onto a sequencing gel.

See figures

Applications

DyeEx Kits remove any type of dye terminator from 10–20 µl sequencing reactions including BigDye, dRhodamine dye, Rhodamine, DYEnamic ET and WellRED terminators. After cleanup, the sequencing reactions can be separated on any capillary sequencer. Signal intensities are high, resulting in long read lengths.

Comparison of DyeEx Kits

Features DyeEx 2.0 Spin Kit DyeEx 96 Kit
Binding capacity 10–20 µl 10–20 µl
Elution volume 10–20 µl 10–20 µl
For DyeEx Kits: Terminator removal, ABI PRISM 377, 373, 310, 3100, or 3700, MegaBACE 1000, or CEQ 2000 sequencers Terminator removal, ABI PRISM 377, 373, 310, 3100, or 3700, MegaBACE 1000, or CEQ 2000 sequencers
Format Tube 96-well plate
Processing Manual Manual
Removal <10mers 17–40mers dye terminator proteins Dye terminator Dye terminator
Sample type Sequencing reactions Sequencing reactions
Technology Gel filtration Gel filtration

DyeEx Kits are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

Supporting data and figures

Resources

Quick-Start Protocols (2)
DyeEx 96 Kit (EN)
PDF (455KB)
Kit Handbooks (1)
(EN) - DyeEx Handbook
PDF (1019KB)
For DyeEx 2.0 Spin Kit and DyeEx 96 Kit 
Safety Data Sheets (1)
Download Safety Data Sheets for QIAGEN product components.

Publications

Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators.
Keller MA; Addya S; Vadigepalli R; Banini B; Delgrosso K; Huang H; Surrey S;
Physiol Genomics; 2006; 28 (1):114-28 2006 Aug 29 PMID:16940433
Isolation and identification of Rickettsia massiliae from Rhipicephalus sanguineus ticks collected in Arizona.
Eremeeva ME; Bosserman EA; Demma LJ; Zambrano ML; Blau DM; Dasch GA;
Appl Environ Microbiol; 2006; 72 (8):5569-77 2006 Aug PMID:16885311
Mammalian monogamy is not controlled by a single gene.
Fink S; Excoffier L; Heckel G;
Proc Natl Acad Sci U S A; 2006; 103 (29):10956-60 2006 Jul 10 PMID:16832060
High throughput analysis of TCR-beta rearrangement and gene expression in single T cells.
Zhou D; Srivastava R; Grummel V; Cepok S; Hartung HP; Hemmer B;
Lab Invest; 2006; 86 (3):314-21 2006 Mar PMID:16446708
Prevalence, risk factor analysis, and follow-up of infections caused by three feline hemoplasma species in cats in Switzerland.
Willi B; Boretti FS; Baumgartner C; Tasker S; Wenger B; Cattori V; Meli ML; Reusch CE; Lutz H; Hofmann-Lehmann R;
J Clin Microbiol; 2006; 44 (3):961-9 2006 Mar PMID:16517884

FAQ

Can the DyeEx 96 kit be used to clean sequencing reactions to be run on ABI 3730?

Yes, DyeEX 96 is also compatible with ABI 3730. When using DyeEx96 with ABI 3730, please follow the  "Modified protocol" listed in the DyeEX Handbook. In addition, if using the waterloading protocol on ABI 3730 sequencer,  the eluate can be loaded directly onto the sequencer without drying down the sample.

FAQ ID -3075
Can DyeEx be used to clean up labeled DNA other than sequencing templates?

DyeEx Kits have been developed for cleanup of dye-terminator sequencing reactions. However, they can also be used for removal of unincorporated nucleotides from radioactively labeled DNA fragments using the protocols in the DyeEx Handbook. The removal of nucleotides depends on the sample volume. Typically, more than 99% of nucleotides are removed from sample volumes ≤50 µl. See Figure 9 in the DyeEx Handbook for the effect of sample volume on recovery.

(We have had feedback from researchers who have reported excellent results using DyeEx for clean up of probes used for in situ hybridization).

FAQ ID -137