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
Add Mag-Bind? SeqDTR? and 85% Ethanol, Mix
Magnetize and remove cleared supernatant
Wash 2x with 85% Ethanol
Elute and transfer DNA to a new plate