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PRIMER
EXTENSION SEQUENCING SERVICE Back
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| 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
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| Result: |
700-1100 bp sequence
data per reaction. |
| |
|
| Starting
Material: |
Purified PCR
products from customer.
Provided
primers from customer. |
| |
|
| Method: |
Primer-extension
by using big-dye chemistry or other
related chemistry from Applied Biosystem. |
| |
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
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| Result: |
Consensus sequence
with > 99% accuracy. |
| |
A complete report
of sequencing strategies and data. |
| |
|
| Starting
Material: |
Provided templates
from customer. |
| |
Customer-provided
initial primers. |
| |
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. |
| |
|
| 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. |
| |
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. |
| |
A complete report
of sequencing strategies and data. |
| |
|
| Starting
Material: |
Templates from
customer. |
| |
Customer-provided
primers. |
| |
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. |
| |
|
| Method: |
Design and synthesize
internal primers. |
| |
Double stranded
coverage of the template through multiple
sequencing reactions. |
| |
Assemble and
edit the contigs? |
| |
The problematic
regions are completely determined. |
| |
The consensus
sequence is generated with accuracy
greater than 99.99%. |
BAC,
PAC AND P1 ENDS SEQUENCING SERVICE
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Result |
400-600 bp sequence
data |
| |
|
| Starting
Material: |
Provided templates
form customer. |
| |
Provided primers
from customer |
| |
|
| Method: |
Proprietary protocols
in conjunction with big-dye chemistry
or other related chemistry from Applied
Biosystems. |
| |
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
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| Result: |
700-1100 bp sequence
data per reaction |
| |
|
| Starting
Material: |
Provided bacterial
cultures or templates from customer. |
| |
Customer-provided
primers. |
| |
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. |
| |
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. |
| |
Use automated
liquid sample handling instrument
to prepare sequencing reactions. |
| |
If the sequence
data is unsatisfactory, the sequencing
reaction is repeated with different
conditions. The better result will
be sent to the customer. |
| |
The samples are
cataloged and stored at -20 celcius
degrees. |
FDA
SUBMISSION SEQUENCING SERVICE
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| Result: |
Finished consensus
sequence with 100 % accuracy. |
| |
A complete report
of sequencing strategies and data. |
| |
|
| Starting
Material: |
Templates from
customer. |
| |
Customer-provided
primers. |
| |
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. |
| |
|
| Method: |
Use big-dye chemistry
or other related chemistry from Applied
Biosystem. |
| |
Complete double
stranded coverage of the template
through 4 fold-redundancy sequencing. |
| |
Resolve all problematic
regions. |
| |
Assemble and
edit the final sequence. |
PLASMID
DNA PURIFICATION SERVICE
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| Result: |
Purified plasmids
suitable for automated sequencing,
transfection, and other molecular
methodologies. |
| |
|
| 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.. |
| |
|
| Starting
Material: |
Crude PCR products. |
| |
Expected size
of the PCR product to be isolated
and purified. |
| |
|
| Method: |
Protocols from
RETROGEN Ultrapure MiniPrep Kit. |
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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