Arrayed and Non-Arrayed BAC library construction
We have been constructing high-quality cDNA and DNA libraries since 1997 and some
of our clients include Agriculture Canada, Pioneer Hi-Bred Int'l (DuPont), Bayer,
Cargill and the Max Planck Institutes in Germany. We guarantee a quick turnaround-time,
unbeatable pricing and large inserts
References are proudly
provided.
An arrayed or non-arrayed BAC library (once arrayed by client) is the preferred
choice for researchers wishing to screen using hybridization techniques. An arrayed
library is also the only template that will do for whole genome sequencing or physical
mapping.
We also offer BAC library construction in custom and shuttle vectors! Please contact
areti@biost.com
Are you planning on screening only for a few target clones? Please visit our
Screened BAC library section with your vector of choice for evaluation.
Highlights
- We typically construct a minimum 5X BAC library which provides a 99.3% probability
of finding the target sequence. Additional coverage and 2-enzyme digestion is available
(additional fee). We pride ourselves in tailoring our services to suit our client’s
needs.
- Coverage is guaranteed. Amount of clones received is based on a guaranteed
coverage and 120Kb average insert size.
- HMW DNA isolation and QC by HMW DNA enzymatic digestion are included.
Deliverables
ARRAYED BAC LIBRARY (WITH CLONE PICK-UP)
- Clones will be arrayed and amplified in 384-well plates (1 unique clone/well), and
shipped on dry ice.
- Genomic coverage is guaranteed.
- Plates will be identified with bar-coded labels.
NON-ARRAYED BAC LIBRARY (WITHOUT CLONE PICK-UP)
- Genomic coverage is guaranteed
- Client will receive BAC clone mixtures (transformed E. coli cells containing
BAC DNA) stored in glycerol and shipped on dry ice.
- An additional 5% of clones will be shipped at no extra charge to compensate for
loss of titer during delivery
- This option is recommended to scientists studying large genomes and/or having arraying
capabilities and/or wishing to limit shipping fees.
Related services
- Nylon filters: Available in small (8x12cm; maximum 3,072 clones) and large size
(22.5x22.5cm; maximum 18,432 clones). Minimum order is 3 sets. The nylon filters
will be ready for hybridization with the clones, in duplicate, cross-linked to them
(Amersham Hybond-N+).
- BAC library copy: Available for the arrayed BAC library option only. A copy of the
Master BAC library can be made and stored or shipped.
- NEW Super pools and Pools Package derived from Arrayed BAC library: We can also
provide the following pools which will allow client to immediately begin screening:
- Plate Pools
- Superpools
- Row pools from Superpool plates
- Column pools from Superpool plates
- Please see
Super pools and Pools Package for more details.
Our strengths
- We guarantee coverage.
- High average insert and even insert size distribution (see Graph 2 below).
- We perform HMW DNA extraction at our facilities.
- We have experience with plant, fungal, bacterial and animal libraries.
- We have extensive experience with GC-rich organisms and marine bacteria.
- Our arrayed BAC libraries are shipped in bar-coded microplates.
- We have extensive experience shipping worldwide.
- Shipment temperature of non-arrayed libraries is always monitored using a BLUE FLAG
Temperature Data logger.
- We provide technical support.
- BAC libraries are the client's property and are never used internally,
sold or distributed.
- We provide references
Table 1: A few libraries constructed in the past with obtained average insert sizes.
|
Starting material
|
Insert size
|
|
Musmusculus
|
180 Kb
|
|
Zea mays
|
150 Kb
|
|
P. brassicacearum
|
160 Kb
|
|
P. omnivore
|
185 Kb
|
|
Arabidopsis thaliana
|
150Kb
|
|
Homo sapiens
|
215 Kb
|
Figure 1: PFG following NotI digestion of insect BAC clones ( Mamestra configurata
) with an average insert size of 178Kb
Figure 2: PFG following NotI digestion of fungal BAC clones P. omnivora) with
an average insert size of 185Kb.
Graph 1: BAC clone insert size distribution (average of 140Kb) of a Soybean BAC
library (Glycine max).
Quote request
Please email our Project Manager, Ms. Areti Karadimos, at
areti@biost.com and include the following details. A quote will be provided
in less than 24 hours.
- - Name of organism of interest.
- - Type of available starting material (leaves, cells, biopsy tissue, etc.)
- - Is starting material limiting?
- - What is the intended use for the BAC library (short-term and long-term if applicable).
- - Known or estimated genome size of species of interest (haploid).
- - Desired genomic coverage.
Importance of a BAC library
BAC libraries are essential elements in doing large-scale genome research such as
genome sequencing, physical maps, and gene cloning. Bacterial artificial chromosomes
(BAC) cloning technology was developed in early 1990s and quickly gained popularity.
This technology was used in applications for genomic analysis that included large-scale
physical mapping and genomic sequencing although this technology was developed much
later than Yeast Artificial Chromosome (YAC) and cosmid cloning technologies. This
should be attributed to the technical advantages of BAC cloning over YAC and cosmid
cloning system summarized as follows:
- Bigger insert size (up to 300 kb) than cosmid and other plasmid system.
- Much more stable than yeast.
- Bacterial clones and libraries grow much faster than YAC.
- Easier in handling and gridding, DNA preparation.
- We have extensive experience with GC-rich organisms and marine bacteria.
- Our Allows for more efficient screening by either hybridization or PCR based screening.sive
experience shipping worldwide.
The major applications of BAC library construction are in large-scale
physical mapping and genomic sequencing and encompass the following applications:
Isolation of Gene clusters for entire metabolic pathway
A BAC library can be employed to scan for gene pathways in drug discovery, gene
pathways in various diseases, plant genetics and microbial metabolic pathways. A
variety of applications derive from construction of BAC libraries including BAC
Macro arrays, gene isolation by pooled PCR, homology based hybridization using various
DNA probes.
Prepare FISH probes
Fluorescence In Situ Hybridization (FISH) employs BAC vectors as probes to illumine
and analyze tissue samples to understand chromosomal rearrangements, amplifications,
deletions and aneusomies. Usually fluorescent probes for specific section(s) of
a chromosome are used to label a locus of a chromosome within a cell sample where
the specified genetic sequences are found.
Complementation for map-based gene cloning using Binary vector in plants
A BAC library can be used to interrogate the genetic structure of plant genomes
as well as mutant genotype analysis using complementation techniques. This endows
the scientist with a reliable tool to study global gene expression in plant species
and to isolate individual genes.
Genomic walking
This allows direct genome sequencing using BAC libraries instead of sequencing
directly from genomes, which is a very difficult proposition and allows study of
gene structure using the entire genome.