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PRIMER EXTENSION SEQUENCING SERVICE Back to top
Result: |
700-1100 bp sequence data per reaction. |
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Starting Material: |
Provided templates from customer. |
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Provided primers from customer |
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Custom primers can be synthesized at our company for faster results. |
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The following universal primers are available to you at no cost: T3, T7, Sp6, M13R, M13F, pGEX3', pGEX5', and BGH reverse. |
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Method: |
Primer-extension sequencing by using big-dye chemistry or other related chemistry from Applied Biosystem. |
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If the sequence data is unsatisfactory, the sequencing reaction is repeated with different conditions. The better result will be sent to the customer. |
DIRECT PCR PRODUCT SEQUENCING SERVICE Back to Top
Result: |
700-1100 bp sequence data per reaction. |
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Starting Material: |
Purified PCR products from customer.
Provided primers from customer. |
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Method: |
Primer-extension by using big-dye chemistry or other related chemistry from Applied Biosystem. |
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If the sequence data is unsatisfactory, the sequencing reaction is repeated with different conditions. The better result will be sent to the customer. |
SINGLE STRANDED DNA SEQUENCING SERVICE Back to Top
Result: |
Consensus sequence with > 99% accuracy. |
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A complete report of sequencing strategies and data. |
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Starting Material: |
Provided templates from customer. |
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Customer-provided initial primers. |
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Custom primers can be synthesized at our company for faster results. |
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The following universal primers are available to you at no cost: T3, T7, Sp6, M13R, M13F, pGEX3', pGEX5', and BGH reverse. |
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Method: |
Design and synthesize internal primers at the optimal interval for better overlap. |
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Single stranded coverage of the template through multiple sequencing reactions. |
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Assemble and edit the contigs? |
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Resolve most problematic regions. |
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The consensus sequence is generated with accuracy greater than 99 %. |
DOUBLE STRANDED DNA SEQUENCING SERVICE Back to Top
Result: |
Finished consensus sequence with greater than 99.99% accuracy. |
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A complete report of sequencing strategies and data. |
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Starting Material: |
Templates from customer. |
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Customer-provided primers. |
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Custom primers can be synthesized at our company for faster results. |
|
The following universal primers are available to you at no cost: T3, T7, Sp6, M13R, M13F, pGEX3', pGEX5', and BGH reverse. |
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Method: |
Design and synthesize internal primers. |
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Double stranded coverage of the template through multiple sequencing reactions. |
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Assemble and edit the contigs? |
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The problematic regions are completely determined. |
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The consensus sequence is generated with accuracy greater than 99.99%. |
BAC, PAC AND P1 ENDS SEQUENCING SERVICE Back to Top
Result |
400-600 bp sequence data |
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Starting Material: |
Provided templates form customer. |
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Provided primers from customer |
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Method: |
Proprietary protocols in conjunction with big-dye chemistry or other related chemistry from Applied Biosystems. |
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If the sequence data is unsatisfactory, the sequencing reaction is repeated with different conditions. The better result will be sent to the customer. |
cDNA/EST LIBRARY SEQUENCING SERVICE Back to Top
Result: |
700-1100 bp sequence data per reaction |
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Starting Material: |
Provided bacterial cultures or templates from customer. |
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Customer-provided primers. |
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Custom primers can be synthesized at our company for faster results. |
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The following universal primers are available to you at no cost: T3, T7, Sp6, M13R, M13F, pGEX3', pGEX5', and BGH reverse. |
|
If the sequence data is unsatisfactory, the sequencing reaction is repeated with different condition. The better result will be sent to the customer. |
Method: |
Primer-extension by using big-dye kit or other related chemistry from Applied Biosystem. |
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Use automated liquid sample handling instrument to prepare sequencing reactions. |
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If the sequence data is unsatisfactory, the sequencing reaction is repeated with different conditions. The better result will be sent to the customer. |
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The samples are cataloged and stored at -20 celcius degrees. |
FDA SUBMISSION SEQUENCING SERVICE Back to Top
Result: |
Finished consensus sequence with 100 % accuracy. |
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A complete report of sequencing strategies and data. |
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Starting Material: |
Templates from customer. |
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Customer-provided primers. |
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Custom primers can be synthesized at our company for faster results. |
|
The following universal primers are available to you at no cost: T3, T7, Sp6, M13R, M13F, pGEX3', pGEX5', and BGH reverse. |
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Method: |
Use big-dye chemistry or other related chemistry from Applied Biosystem. |
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Complete double stranded coverage of the template through 4 fold-redundancy sequencing. |
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Resolve all problematic regions. |
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Assemble and edit the final sequence. |
PLASMID DNA PURIFICATION SERVICE Back to Top
Result: |
Purified plasmids suitable for automated sequencing, transfection, and other molecular methodologies. |
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Starting Material: |
Provided bacterial cultures or agar plates from customer. |
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Method: |
Protocols from RETROGEN Ultrapure MiniPrep Kit. |
PCR PRODUCT PURIFICATION SERVICE Back to Top
| Result: |
Purified PCR fragments are suitable for automated sequencing.. |
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| Starting Material: |
Crude PCR products.
Expected size of the PCR product to be isolated and purified |
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| Method: |
Protocols from RETROGEN Ultrapure MiniPrep Kit. |
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SHOTGUN LIBRARY CONSTRUCTION & SEQUENCING Back to Top
| Result: |
Original electropherograms |
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Consensus sequence on diskette |
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| Starting Material: |
Shotgun sequencing strategies can be used to sequence a variety of samples including cosmids, BACs, PACs, and genomics. |
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| Method: |
Randomly generated plasmid clones using nebulization techniques. |
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The random fragments (typically, 1-3 kb in length) are cloned into a standard vector with common restriction sites. |
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Sequence data is obtained from each end of the random clones and assembled to provide up to 100% coverage of the entire clone. |
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Contig alignment of each gel read |
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