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<M1300> Mag-Bind SeqDTR 用磁珠純化方式高通量地去除自動測序前的游離熒光染料探針

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Mag-Bind? SeqDTR is designed to effectively and reliably remove unincorporated terminators from sequencing reactions. The system combines Omega Bio-tek's proprietary chemistries with the reversible nucleic acid-binding properties of magnetic beads to eliminate excess nucleotides, primers, and small, non-targeted amplification products such as primer dimers.

用磁珠純化方式高通量地去除自動測序前的游離熒光染料探針 

Mag-Bind SeqDTR


產品編號

產品名稱

包裝規格

目錄價

M1300-05

   用磁珠純化方式高通量地去除自動測序前的游離熒光染料探針     

5ml

1700

M1300-08

用磁珠純化方式高通量地去除自動測序前的游離熒光染料探針  

50ml

9350

M1300-50

用磁珠純化方式高通量地去除自動測序前的游離熒光染料探針  

500ml

76500



產品介紹

Mag-Bind? SeqDTR is designed to effectively and reliably remove unincorporated terminators from sequencing reactions. The system combines Omega Bio-tek's proprietary chemistries with the reversible nucleic acid-binding properties of magnetic beads to eliminate excess nucleotides, primers, and small, non-targeted amplification products such as primer dimers. Sequencing products are mixed with the Mag-Bind SeqDTR magnetic particles, which selectively bind DNA. Two rapid wash steps eliminate trace contaminants such as nucleotides and primers to reduce background signal and, therefore, achieve higher QV scores.

The high sensitivity of Mag-Bind SeqDTR’s binding ability allows for decreased concentrations of BigDye? chemistry to be used and longer continuous read lengths to be achieved. Mag-Bind SeqDTR can be processed in 96- and 384-well formats and is compatible with many liquid handling instruments, including Hamilton Microlab? STAR? & STARlet?, Beckman Coulter Biomek? FX & NX, and Tecan Evo instruments. Up to 4 plates can be run in a 96-well format in less than 25 minutes.

  • No protocol change against major competitor

  • Read lengths averaging over 800 bps (Min Phred 20)

  • Manual or adjustable to automated liquid handlers

  • Significant cost savings compared to sephadex-based clean ups

  •  96- or 384-well formats




參數

FEATURES

SPECIFICATIONS

Downstream application

Sanger Sequencing, Cloning, In Vitro Transcription, Nucleic Acid Labeling, PCR, Real-Time Quantitative PCR (qPCR), Sequencing, Southern Blotting

Elution volume

40 μL of Elution Buffer for 96-well plate protocol. 15–20 μL of Elution Buffer for 384-well plate protocol.

Starting material

ABI Big Dye Chemistry Cycle Sequencing Reactions

Starting amount

5 – 20 μL

DNA recovery

Sequencing reads start at 40 nt

Processing mode

Automated; Manual

Throughput

96–384 samples per run

DNA binding technology

Magnetic beads

Binding capacity

Scalable

Storage

2°C – 8°C


組分

ProductNo.

M1300-05

M1300-08

M1300-50

Mag-Bind? SeqDTR?

5 ml

50 ml

500 ml

Preparations

500* / 1,000**

5,000* / 10,000**

50,000* / 100,000**

User Manual

?

?

?

*   Based on a typical 10 μL reaction volume in a96-well format

** Based on a typical 5 μL reaction volume in a 384-well format


流程

  1. Add Mag-Bind? SeqDTR? and 85% Ethanol, Mix

  2. Magnetize and remove cleared supernatant

  3. Wash 2x with 85% Ethanol

  4. Elute and transfer DNA to a new plate