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Holding
Vector types
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Expression vectors and gene inserts, incl. mutants
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such as, but not limited to
- cloning vectors
- basic expression vectors
- gateway expression vectors
- dicistronic expression vectors
- adenoviral expression vectors
- retroviral expression vectors
- yeast two-hybrid expression vectors
- yeast three-hybrid expression vectors
- reporter gene vectors
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such as, but not limited to
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cytokines (TNF, IL-1β, IL-2, IL-4, IL-5, IL-6, IFN-β, LT, …)
- cytokine receptors (TNF-R1, TNF-R2, Fas)
- GTP-binding genes (Cdc42, RhoA, Rac1)
- ubiquitin related genes (Ubc9, UbB)
- promoter reporter gene constructs and mutants (IL-6, NF-κB, caspase-11, E-cadherin, …)
- apoptosis signaling related genes (RIP1, TRADD, FADD, caspases, CrmA, Bcl-2 family members, …)
- NF-κB signaling related genes (IRAK1, IRAK4, RIP1, RIP2,TRAF2, IKKα, IKKβ, NEMO, p65, Gal4-p65, ABINs, A20, TAX1BP1, …)
- toll-like receptor signaling related genes (TLR3, MyD88, TRIF, Mal, TRAM, …)
- bacterial type III secretion system related genes (exoS, exoT, sopE, yopE, yopP, …)
- IRES sequences and IRES-transactivating factors (PTB, UNR, PITSLRE kinase, hnRNPC1/C2, …)
- N-glycosylation related genes (Angls2, Ppgls2, Scgls2, Trgls2, GlcNAc-TI, cbhI, TS)
- monoamino-oxidase genes (MAOA, MAOB)
- toxin-related genes (CNF1)
- lipoprotein related genes (APOA1)
- hairpin RNA expression plasmids for genome-wide gene silencing in Arabidopsis thaliana
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All publicly available plasmids are described in full
molecular detail and are submitted to quality control tests (purity, viability
and authenticity (restriction site analysis))
- A selection of recommended or required bacterial host
strains.
- DNA libraries, from fungal to human origin. The DNA libraries are oligo(dT) and/or random hexamer primed,
and most often cloned in an oriented way in an expression cassette.
Services
All assignments, with exception of deposits of
microbial resources for public access, are treated strictly confidential.
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Public deposit
BCCM/LMBP accepts for public deposit:
- plasmids
- bacterial host strains
- DNA libraries
Before sending material, it is advisable to contact
BCCM/LMBP to make sure that the material to be
deposited is within its scope and technical capabilities and to be informed of the necessary form and quantity of the material.
Upon public deposit of plasmids, the depositor must complete the Accession Form F103.
Upon public deposit of bacterial host strains, the depositor must complete the Accession Form F104.
Upon public deposit of DNA libraries, please contact BCCM/LMBP.
Deposits for public access are without costs for
the depositor.
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Safe deposit
BCCM/LMBP accepts for safe deposit:
- any kind of natural or recombinant plasmid or
genetic material, either in a purified form or
within a host, not exceeding risk class 2
- natural or genetically modified animal cell lines,
including human cell lines and hybridomas, not exceeding risk class 2
Before sending material, it is advisable to contact
BCCM/LMBP to make sure that the material
to be deposited is within its scope and technical capabilities and to
be informed of the necessary form and quantity of the material.
Upon safe deposit of plasmids, the depositor must complete the contract F405.
Upon safe deposit of cell lines and hybridomas, the depositor must
complete the contract F073.
Upon safe deposit of other resources, please contact BCCM/LMBP.
For extension of safe deposit contracts for a predefined period, the
depositor will be contacted by BCCM/LMBP.
For termination of safe deposit contracts for an undefined period, the
depositor must complete the form F408.
For related costs see pricelist.
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Patent deposit
BCCM/LMBP accepts for patent deposit:
- any kind of natural or recombinant plasmid or
genetic material, either in a purified form or
within a host, not exceeding risk class 2
- natural or genetically modified animal cell lines,
including human cell lines and hybridomas, not exceeding risk class 2
Before sending material, it is advisable to contact BCCM/LMBP to make sure that the
material to be deposited is within its scope and technical capabilities
and to be informed of the necessary form and quantity of the material.
Upon patent deposit, the depositor must complete the international
Accession Form BCCM/LMBP/BP/1 as
well as the bilateral contract Form BCCM/LMBP/DBT1.
Once BCCM/LMBP has accepted the material and confirmed
its viability and purity, it will send to the depositor or to the party
designated on form BP/1, the completed international forms BCCM/LMBP/BP/4
(receipt of an original deposit) and BCCM/LMBP/BP/9 (viability statement).
These documents constitute the proofs of the deposit.
See also the detailed Manual
for the deposit of Biological Material for Patent Purposes under the Budapest
Treaty.
For related costs see pricelist.
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Storage of third party’s biological material
BCCM/LMBP accepts for storage of third party’s biological material:
Before sending material, it is advisable to contact BCCM/LMBP to make sure that the material to be deposited is within its scope and technical
capabilities and to be informed of the necessary form and quantity of the material.
Upon storage, the depositor must complete the contract F411 with annex F412.
For extension of storage contracts for a predefined period, the depositor will be contacted by BCCM/LMBP.
For termination of storage contracts for an undefined period, the depositor must complete the form F413.
For related costs see pricelist.
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Distribution of biological material from the public, safe deposit or patent deposit collection
Resources of the public collection
are accessible to the scientific community under the conditions of the
BCCM Material Transfer Agreement (MTA),
if necessary amended with additional conditions possibly already attached
to the biological material.
For more information on ordering microbial resources click here.
Consult the BCCM/LMBP catalogues to search the resources you require.
Resources of the safe deposit collection
are not catalogued and are only available to the depositor or to third
parties with the written authorization of the depositor.
For related costs see pricelist.
The distribution of samples of biological
material deposited under the Budapest Treaty for patent purposes
depends on the authorization by the depositor or an entitled Industrial
Property Office. Patent deposits are not catalogued.
For related costs see pricelist.
Accession, control, preservation, storage and supply of plasmids and bacterial hosts and related information
in the frame of public deposits, research deposits, safe deposits and patent deposits are ISO 9001:2008 certified.
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Distribution of TRC 1/1.5 human and mouse shRNA libraries
Following the 2009-2010 call of the Hercules Foundation for medium-scale research infrastructure1, BCCM/LMBP became a partner in a collaboration of scientists of the Ghent University and the VIB who are working in the domain of life sciences and have already extensive experience with the use of RNA interference (RNAi).
RNAi has become an essential tool for functional genomics. It permits the selective knock-down of specific proteins in cells to assess their functional role. RNAi serves to discover proteins involved in a particular cell function or signal transduction pathway. It is increasingly used to discover and validate new targets and biomarkers, and to elucidate disease mechanisms. Moreover, it is being developed for in vivo experimental use and even for therapeutic use.
Via BCCM/LMBP all researchers of the Ghent University and VIB gain easy and unlimited access to individual bacterial glycerol stocks of the genome-wide SIGMA MISSION TRC1 human and mouse libraries, consisting of over 176.000 pre-cloned shRNA vectors targeting more than 16.000 human and 15.950 mouse genes.
More info: bccm.lmbp@dmbr.UGent.be
Template structure of each shRNAi clone
Ordering procedure
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for VIB researchers: consult the VIB intranet under the topics 'VIB Technologies > 3. Protein analysis > 9. Human and mouse gene shRNA plasmids'
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for DMBR researchers: consult the DMBR intranet under the topics 'Research > Core Facilities > BCCM Plasmid Collection', after logging in
for Ghent University researchers: click here
1 Set up in 2007 by the Flemish Government as a structural funding instrument for investments in research infrastructure.
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Plasmid profile analysis
By default, this customized contract service allows the analysis of non-pathogenic,
bacterial strains for the presence of natural, middle- and high-copy number plasmids of max. 20.000 bp by agarose gel electrophoresis of non-digested plasmid DNA.
Before sending material, it is advisable to contact BCCM/LMBP to make sure that the material to be analysed
is within its scope and technical capabilities, to discuss extra requirements (e.g. low copy plasmid profile, large plasmids profile, …)
and to be informed of the price offer.
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ProfileThoseSugars - Analysis of protein-linked glycans on DNA sequencing equipment
Carbohydrates, like DNA and proteins, can be separated
electrophoretically on polyacrylamide gels. To allow detection, and in
some cases to add charge, the oligosaccharides are fluorescently labelled.
Classical FACE (fluorophore assisted carbohydrate electrophoresis) allows
separation and detection of oligosaccharides, though with relatively low
sensitivity and poor resolving power. A major breakthrough came when slab
gel DNA-sequencing equipment was successfully used for the profiling and
analysis of oligosaccharides. When an appropriate fluorescent dye is used,
usually APTS, 8-aminopyrene-1,3,6-trisulfonic acid, DSA-FACE (DNA–Sequencer
Aided FACE) allows separation with high resolution and sensitivity. Importantly,
many isomeric and isobaric structures can be separated. Moreover, the
high sensitivity permits the use of minute amounts of glycoproteins for
the analysis of all the attached glycans. Now that this technique is available,
high throughput analysis of biological samples becomes possible, and its
use in glycodiagnosis is emerging.
Customized contract analytical services (specializing
in miniaturized comparative analysis of larger series of samples) built
on this technology and performed by the developers, are available now
through the ProfileThoseSugars service at BCCM/LMBP.
For related costs see price scheme.
The protocol for the ProfileThoseSugars service
on the Applied Biosystems gel-based or capillary array-based DNA sequencers,
has been published in detail in Nature Protocols:
W. Laroy, R. Contreras and N. Callewaert, 2006.
Glycome mapping on DNA sequencing equipment. Nature Protocols, Vol.1,
No.1, 397-405.
In concert with Prof. Dr N. Callewaert and his team, we will be happy to discuss your glycoanalysis requirements and advise you on the most appropriate strategies and the options suitable for your specific research needs.
Before sending samples and the accompanying order form, please contact BCCM/LMBP to sign a services agreement.
Scientific context
Organisation chart

Further information & contact
Promoter: Prof. Dr Rudi Beyaert
Scientific Advisor: Prof. Dr Erik Remaut
Manager: Lic. Martine Vanhoucke
Curator: Lic. Martine Vanhoucke
Contact:
Lic. Martine Vanhoucke
BCCM/LMBP
Department of Biomedical Molecular Biology
Ghent University
Technologiepark 927
B-9052 Zwijnaarde ( map
& directions)
Phone: +32-9-33.13.843
Fax: +32-9-33.13.504
E-mail: bccm.lmbp@dmbr.UGent.be
2011 Holidays:
The BCCM/LMBP collection will be closed during the following dates ( click
here).
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