Manuel Nucleic acid isolation
Analytik Jena offers an extraordinary wide range of purification and isolation kits for nucleic acids, all made in Germany. Those are based on own technologies and patents. It ranges from manual to automated solutions for DNA/RNA extraction of most starting materials.

For fast and efficient purification of PCR products from PCR reaction mixtures based on a new two-step-procedure (bind and elute). No washing steps are necessary. Using 96 well filterplates in combination with a centrifuge the kit allows the purification of up to 96 samples parallel. The whole procedure is ready within 30 minutes.
For fast and efficient purification of PCR products from PCR reaction mixtures based on a new two-step-procedure (bind and elute). No washing steps are necessary. The whole isolation is finished within 3 minutes, only.
For extraction and recovery of DNA fragments from TAE or TBE agarose gels.
For fast and efficient purification of PCR products from PCR reaction mixtures based on a new two-step-procedure and/or for the extraction and recovery of DNA fragments from TAE or TBE agarose gels.
For fast removing of dye terminators from sequencing mixes based on a new two-stepprocedure (bind and elute). No washing steps are necessary. No ethanol precipitation or sephadex.
For isolation of high yield plasmid DNA from 5 – 15 ml bacteria suspension. The kit uses the fast and effective Spin Filter mini format to isolate up to 40 µg of high-quality plasmid DNA.
For the fast and direct isolation of plasmid DNA from 250 µl of a bacteria suspension. The kit doesn‘t need the pelleting of bacteria cells and starts directly with the bacterial suspension. The kit allows the isolation of 1 – 4 µg plasmid DNA.
For the fast and direct isolation of plasmid DNA from 250 µl of a bacteria suspension. The kit doesn‘t need the pelleting of bacteria cells and starts directly with the bacterial suspension. The kit allows the isolation of 1 – 4 µg plasmid DNA.
For very fast and efficient isolation of genomic DNA from small amounts of different types of starting material like microbiopsies, whole blood up to 50 µl, blood sticks and from limited amounts of cells.
For isolation of genomic DNA from rodent tails. The protocol has been specially optimized to get a maximum yield and quality of genomic DNA from rodent tails.
For isolation of genomic DNA up to 100 mg of different kinds of plant material. The kit combines the lysis of starting material, filtration of unlysed components and subsequent binding of genomic DNA on a Spin Filter surface. After washing the bound DNA will be eluted from the Spin Filter.
For isolation of genomic DNA from whole blood samples from 0.5 ml up to 5 ml using simple Spin Filter mini format. The kit combines the selective lysis of erythrocytes, pelleting of nucleus containing blood cells. After red blood cell lysis the collected lymphocytes will be transfered into a Lysis Tube PLP. The Lysis Tube PLP contains solid formula of proteolytic reagents. No reagents have to be added for the lysis step. After lysis of cells proteins will be removed by selective precipitation following binding of the genomic DNA on a Spin Filter
surface and elution of the bound DNA. Because of the mini Spin Filter format the whole procedure is very fast and efficient and takes place in a standard table centrifuge. The kit allows the isolation of more than 100 µg genomic DNA.
For isolation of genomic DNA from whole blood samples from 0.5 ml up to 2.0 ml. The kit combines the selective lysis of erythrocytes, pelleting of nucleus containing blood cells and subsequent lysis of the cells and protein removing following binding of the genomic DNA on a Spin Filter surface and elution of the bound DNA.
For isolation of genomic DNA direct from whole blood samples up to 300 µl.
For very fast and efficient isolation of genomic DNA from small amounts of different types of forensic samples like hairs or hair roots, stains of blood, saliva or sperm, finger nails, cigarette butts, bubble gum, buccal swabs, stamps and envelopes as well as fingerprints on different surfaces. The kit is a very efficient tool for isolation of DNA for applications where only limited amounts of starting material and very dirty material is available. Further, the new kind of extraction chemistry allows particularly the recovery of degraded DNA.
Every buccal swab is packed separately and sterile in a tube with an inscription field. It consist of wood and cotton. A buccal swab is the easiest way to collect samples of different origin and source and provides so an extensive possibility to get human and animal samples. The assay can be handled and transported easily and is protected against contamination.
For the very fast and efficient isolation of high yield genomic DNA from buccal swabs. The
recovery of DNA and the quality are excellent. The kit contains also swabs for sample
collecting.
For very fast and efficient isolation of genomic DNA from different amounts and different
types of starting material like tissue samples up to 50 mg, paraffin embedded tissue mate-
rial, buccal swabs, mouse or rodent tail, eucaryotic cell pellets.
For very fast and efficient parallel isolation of genomic DNA and cellular total RNA from eucaryotic cells, bacteria and tissue samples.
For very fast and efficient isolation of cellular total RNA from eucaryotic cells, bacteria and tissue samples.
For very fast and efficient isolation of cellular total RNA incl. isolation of small RNA molecules from eucaryotic cells, bacteria and tissue samples.
For very fast and efficient parallel isolation of genomic DNA and cellular total RNA from eucaryotic cells, bacteria and tissue samples.
For very fast and efficient isolation of cellular total RNA from 0.5 ml – 1.0 ml of whole blood.
For very fast and efficient isolation of cellular total RNA from different types of plant material.
For isolation of DNA from pellets of gram+ and gram– bacteria after cultivation. The extraction procedure combines a lysis step with lysozyme following Proteinase K digestion and subsequent efficient binding of genomic DNA on a Spin Filter surface. The bound DNA will be washed and finally eluted.
For isolation of viral RNA from serum, plasma or other cell-free body fluids, from tissue samples, paraffin embedded samples, swabs and from cell cultures.
For isolation of viral DNA from serum, plasma or other cell-free body fluids, from tissue samples, paraffin embedded samples, swabs and from cell cultures. The extraction procedure is based on a new kind of chemistry, which combines an extreme fast lysis step with a subsequent efficient binding of genomic DNA on a Spin Filter surface following washing of the bound DNA and finally eluting of the DNA.
For isolation of DNA from mycobacteria contained in sputum, bronchoalveolar lavage and lymph note samples. The extraction procedure combines optional a sample pre-treatment with N-actetylcysteine, pelleting of bacteria and subsequent bacteria lysis with lysozyme, following Proteinase K digestion and subsequent efficient binding of the DNA on a Spin Filter surface. The bound DNA will be washed and eluted.
For isolation of DNA from pellets of gram and gram bacteria after cultivation. The extraction procedure combines a lysis step with lysozyme, following Proteinase K digestion and subsequent efficient binding of genomic DNA on a Spin Filter surface. The bound DNA will be washed and eluted.
Kit for simultaneously isolation of viral DNA and RNA from different kinds of clinical specimen.
For isolation of viral RNA from serum, plasma or other cell-free body fluids, from tissue samples, paraffin embedded samples, swabs and from cell cultures.
For isolation of viral DNA from serum, plasma or other cell-free body fluids, from tissue samples, paraffin embedded samples, swabs and from cell cultures. The extraction procedure is based on a new kind of chemistry, which combines an extreme fast lysis step with a subsequent efficient binding of genomic DNA on a Spin Filter surface following washing of the bound DNA and finally eluting of the DNA.
For isolation of DNA from mycobacteria contained in sputum, bronchoalveolar lavage and lymph note samples. The extraction procedure combines optional a sample pre-treatment with N-actetylcysteine, pelleting of bacteria and subsequent bacteria lysis with lysozyme following Proteinase K digestion and subsequent efficient binding of the DNA on a SpinFilter surface. The bound DNA will be washed and eluted.
For isolation of bacterial DNA from stool samples. The kit combines a very efficient lysis of starting materials following a pre-filtration step to remove unlysed particles. After prefiltration the sample will be transferred onto a Spin Filter unit and the DNA will be bound on the Spin Filter surface. After washing of the bound DNA the DNA will be eluted from the Spin Filter and is ready to use for further downstream applications.
For very fast isolation of INFLUENZA RNA from primary samples of tracheal swabs or organ grid stored under medium (e. g. enrichment medium). After sample lysis the viral RNA will be bound onto a Spin Filter surface following washing steps and finally eluting of the bound RNA.


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