KISS - keep
it simple and smart - Kits of the MOSAIC Series :
MOSAIC - series cloning kits
are the most basic
standard line for molecular engineering -
fast and reliable and high throughput simply designed to guarantee
simple
handling - nothing else.
| The MOSAIC-FBR-kit | |
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FBR
(Fragmentation
Blending
Reassembling)
for functional improvements of gene products. Mixtures of
homologous DNA populations are cut at random (Fragmentation). DNA
populations can be derived from selected gene families, by error prone
PCR or by synthetic genes. Chemical cleavage at Thymidine
positions generates highly complex heterogeneous blends of
single stranded DNA sequences. (Blending).
By reassembling DNA fragments recombination events are induced.
These are suitable for new combinations of internal new point
mutations to be formed (Reassembling).
These events provide an increased probability of generating
functional complementations improving intended features of gene
products like proteins or RNA. (Reorder # : KT060616FBR). In
combination with the ERM - Kit (Reorder # : KT060616ERM) this
powerful tool provides increased probability for functional
improvements in gene products like protein or RNA.
Lit.:Müller et.al. (2005) Nucleotide exchange and excision
technology (NExT) DNA shuffling: a robust method for DNA
fragmentation and directed evolution. NAR 13:e117.Reorder #: KT060616FBR [Order] |
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| The MOSAIC-ERM-kit | |
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ERM
: Error-prone Random Mutagenesis is
designed for equally distributing point mutations into functional gene
sequences. Transitions (Py→Py, Pu→Pu) and transversions (Py→Pu, Pu→Py)
are intended to be induced at the same frequency. Starting from the
DNA-level, random mutagenesis during molecular synthetic amplification
induces increasing sequential errosions in integrity. Reorder # :
KT060616ERM. In combination with the FBR - kit (Reorder # :
KT060616FBR) powerful tools are provided for increasing the probability
for functional improvements in gene products like protein or RNA.
Cadwell and Joyce (1994) Mutagenic PCR. PCR Methods Appl. 6:136-40,
Spee, J. et al. Nucleic Acids Research, 1993, Vol. 21, No. 3 777-778.
Reorder #: KT060616ERM [Order] |
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| The MOSAIC-UFL-kit | |
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| UFL-standard kit (Universal Fragment Linking) for simple and fast
ligation of any blend and all
kinds of DNA fragments and cycling products of Polymerases (like Taq)
and proof-reading polymerases (like Pfu or Pwo).
This unifying kit is sufficient for making compatible blunt, sticky or
3'-T overhangs for ligation. Even large PCR products can be cloned. A
cloning vector pFUC1 (2695 bp, pUC derivative, blue/white screening,
M13 forward and reverse primer) is supplied linearized and activated
for ligation for direct and efficient cloning in a minimum of time.
Quality checked and certified.
Reorder #: KT060616UFL [Order] |
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| The MOSAIC-RFL-kit | |
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RFL standard kit (Rapid Fragment Linking) for simple and fast ligation of any blend and all kinds of DNA fragments and cycling products of Polymerases (like Taq) and proof-reading polymerases (like Pfu or Pwo). This unifying kit is sufficient for making compatible blunt, sticky or 3'-T overhangs for ligation. Even large PCR products can be cloned. A cloning vector pFUC1 (2695 bp, pUC derivative, blue/white screening, M13 forward and reverse primer) is supplied linearized and activated for ligation for direct and efficient cloning in a minimum of time in most cases 1 min. Quality checked and certified. Most text, 'cause this is the really incredible kit whose name is RFL-kit and it is so beautiful and so on. Reorder #:KT060616RFL [Order] |
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| The MOSAIC-CFS-kit | |
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| CFS colony fast screening kit for
recombinant clone-based plasmid size simple and fast detection of
high- and low-copy E. coli plasmids and identification of
recombinant plasmid inserts as well as fast calculation of cloning
efficiencies. Minipreps are OUT. Screening is performed directly using
the primary colonies after transformation. One colony is sufficient for
screening. Results are achieved within less than one hour by simple
agarose gel electrophoresis.
Reorder #:KT060616CFS [Order] |
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| The MOSAIC-HCE-kit | |
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| HCE highly chemo-competent E. coli cell: an
everyday efficiency tool: chemically competent cells
Remove your bottleneck. Cloning and transformation results are as
good as the competent cells used.
We provide you the reliable standard of high quality chemically
competent cells.
Reorder # : KT060616HCE [Order] |
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| The Medium-OSM-kit | |
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| Medium - OSM (Optimum Solubility Medium) - Rich medium to
increase solubility of proteins and reduce foam during cultivation and
recombinant expression in E. coli.
During recombinant expression in the common host E. coli,
many proteins have the tendency to aggregate as insoluble inclusion
bodies.
Since these proteins are not in the native and mostly desired
conformation, difficult denaturation and renaturation steps are
necessary to obtain a soluble protein with correct conformation.
Unfortunately, these renaturation steps are very time consuming and
results as well as the final yield could not be predicted.
Therefore, the expression of a soluble and correctly folded recombinant
protein is most likely desired.
The medium "OSM" increases the amount of soluble protein during
recombinant expression. OSM is available as ready-to-use liquid medium
as well as powder for preparation of medium.
Reorder #: KT060616OSM [Order] |
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Choose one of the following ways to order:
1. Use the ordering form below.
2. Call us (+49-761-8889424).
3. Email us @ info@atg-biosynthetics.de
4. Ask your purchasing department to fax us (+49-761-8889425) the valid purchase order number.
5. ATG:biosynthetics adopt a non-disclosure policy to all of our
customers. To protect your proprietary information please mail, email
(info@atg-biosynthetics.de) or fax (832-886-5152) your confidentiality
agreement to us for signing. If intended, this should be done before any
information is released to us. If you don't have your own
NDA/confidentiality agreement, you can find
ours here. Feel free to modify it to suit your specific needs.
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