Agencourt CleanSEQ produces high sequencing pass rates and average Phred20 read purification system with a simple three-step protocol. The. Agencourt. Solid Phase Reversible Immobilization (SPRI) paramagnetic bead-based technology. The Agencourt CleanSEQ method follows a simple three-step protocol that. Program and use the MagSi-DNA cleanFIX protocol as described in the product Make use of the installed Agencourt AMPure® XP and CleanSEQ® protocols.

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Pipette mix 7 times, or seal and prktocol the reaction plate for 30 seconds. The system produces sequences with longer Phred 20 read lengths and higher signal intensities than any other purification technology for Sanger cycle sequencing clean-up.

Are your results reproducible? It is important to completely remove all of the supernatant as it contains excess fluorescent dye and contaminants.

Chemistry guides and trouble shooting Primer availability We offer the following primers for use in sequencing reactions. The CleanSEQ protocol does not require precipitation, filtration or centrifugation. The SPRI technology is easily scaled and automation friendly, allowing both high throughput and format flexibility.

The Personal Staff accompanying the President of India, Primer availability We offer the following primers for use in sequencing reactions. When you are diluting ethanol stock to the working concentration for Agencourt CleanSEQ, make only as much as you will use in 13 days and store it in a tightly capped container.


Decreases in ethanol concentration, due to the absorption of water from the surrounding atmosphere, may lead to a loss of product.

Protocop enough to cause a noticeable impact on the subject’s daily life. We share information about your activities on the site with our partners and Google partners: The optimal elution buffer will vary depending on dye chemistry and reaction conditions. PDF version and updates available from Govnet.

Trouble shooting There are many reasons for a failed or poor quality result. Protocol The Prime Minister of India. Protocol 67 Accordingly, BDR reported the matter to the department board, arguing that the department Email us at sequence lincoln. Complete the form and a supplier representative will be in touch. Aspirate cleared solution supernatant from the reaction plate and discard. The purification procedure is amenable to a variety of automation platforms since it requires no centrifugation or vacuum filtration.

The reagent should appear homogenous and consistent in color.

Data sheet to write down scores. Wednesday, 25 May, Supplied by: Agencourt CleanSEQ contains magnetic particles in an optimized binding buffer to selectively capture sequencing extension products.

Beckman Coulter CleanSEQ dye-terminator removal system

Sequence reaction cleanup protocol We use the Agencourt CleanSEQ magnetic bead-based sequencing purification system to remove unincorporated dyes, nucleotides, salts, and other contaminants after the sequencing reaction. High signals can lead to overloading and EDTA helps to even out sample injection to counteract this effect see Figure 1 on the next page.


Please use table 3 as a general guideline for choosing an elution buffer. Antimicrobials — 20th Annual Scientific Meeting. Prepare primers to 5.

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During the protocol avoid extensive heat, light or waiting time, as this can lead to degradation of the dyes. We recommend you review the electropherogram, annotation and raw data for each cleansew, using programmes such as Sequence Scanner, Sequence Analysis or Chromas to import the.

Protocol Feb 18, – This trial protocol has been provided by the authors to give readers additional information about their work. Elute the samples just prior to loading them on the sequencing detector. Note that excessive drying can lead to degradation of the incorporated dyes. Reagent grade water, 0.

Let the reaction plate air-dry for 10 minutes at room temperature. By Yossi Leon, Project Leader.

Sentiment protocol – a decentralized protocol Refer to figure 2 for the effects of loading solutions. Protocol Sep 29, – Tel: The paramagnetic bead format requires no centrifugation or filtration and is easily performed manually or fully automated protcool high throughput dye-terminator removal. Additionally, we are always willing to address your queries. Statistical analysis plan, summary of changes prior to database lock”