High
Quality Standard cDNA Libraries are produced using our proprietary
technology. First strand cDNA is made from mRNA that is primed using
oligo dT. After the second strand is synthesized, the double stranded
cDNA is size fractionated, cloned directionally into our Express
I vector and transformed into T1 phage resistant E.
coli. We guarantee at least 3x106 primary clones
with 87%
recombinant clones containing an average insert size of at least
1kb, however, we generally produce libraries of 10x106
primary clones with >95% recombinant clones containing 1.5kb
average insert size.
We
will make standard libraries from customer supplied tissue ( 1
g), cells (at least 1x108), total RNA ( 1
mg) or mRNA ( 5 µg).
We provide quality controlled primary or amplified libraries.
Features list:
-
High quality size fractionated cDNA.
- Directionally cloned cDNA for expression, antibody screening,
subtraction and normalization.
- Large numbers of primary clones.
- Low vector background.
Quality
testing: Percentage of recombinant clones and average insert
size determined by gel analysis of 24 clones picked at random.
Shipment and storage conditions: Libraries will
be shipped in dry ice. Storage of libraries at -80°C is recommended.
Characteristics
of a cDNA Library Constructed From a Standard
Amount of HeLa mRNA |
mRNA
(ng) |
Total
# of primary clones |
Average
insert size (kb)* |
Percent
recombinants |
Insert
size range (kb)* |
5,000 |
12.0x107 |
2.24
|
96 |
0.5
- 4.4 |
*Average
insert size and insert size range determined by restriction enzyme
digestion of 24 clones picked at random from each library.
Click
here for Tissue and RNA Preparation suggestions |
|