Applications & Technologies
High Uniformity in BRCA Analysis, Enhanced viability and retention, VIROMER® CRISPR for RNP delivery etc.
High Uniformity in BRCA Analysis, Enhanced viability and retention, VIROMER® CRISPR for RNP delivery etc.
Universal Quality Standards
Digestif comprises a soluble recombinant protein scaffold + 11 artificial peptides (iRT) with good ionization.
Amino acids flanking iRT cleavage site either favour or hinder protease cleavage.
Retention time & relative intensity pattern of released iRT can assess the quality of sample workup, the extent of digestion, LC-MS performance & inter/intra-lab variability
Hybridisation Capture vs PCR Amplification Enrichment in Targeted NGS
Hybridisation capture enrichment in targeted NGS, using a novel probe design technology, increases data uniformity compared to PCR amplification enrichment. Hybridisation capture gives coverage across UTR´s, Promoters, CDS, Splicing sites and enables detection of more mutants; insertions/deletions, CNV´s, SNV´s and gene fusion.
The unique re-balancing process with full QC will ensure optimal design and efficient workflows.
Download comparison data here!
The unique Laminar Wash™ technology simplifies and automates flow cytometry workflows for CAR-T-cell manufacturing. Data improves reproducibility, saves time and gives tighter populations. Laminar Wash™ replaces centrifugation-based stain&wash and is more gentle to cells. Time saving in this workflow was 50 min/assay.
CAR-T cell therapy biotech company AdiCet Bio improved data by automating of a part of their flow cytometry assay. They saw improved consistency and are planning full automation using a Laminar Wash™ system.
Low Abundant Protein Quantification in Complex Matrices
The Promise Proteomics SIL proteins are of high purity and >99% isotopic incorporation. You get an internal standard with the same sequence as your target protein of interest, thus normalising for variation in sample digestion and purification processes.
Get a free poster presenting the LC-MS workflow for quantification of Tau protein (microtubule-associated protein) as a sensitive biomarker for Alzheimer Disease. Get poster here!
The riboPOOL™ offers simultaneous ribo-depletion for complex samples. The method will deplete ribosomal RNA simultaneously across multiple species.
Efficient depletion of human, mouse and E. coli RNA with the Combination riboPOOL consisting of a 1:1:1 mix of Human, Mouse/Rat and Pan-Prokaryote riboPOOL was observed for 1 μg RNA input.
The Pan-Prokaryote riboPOOL gives the widest microbial coverage for microbiome/metagenomic analysis, covering >75 different species simultaneously. Removing ribosomal RNAs (rRNAs) with high efficiency and targets 5S, 16S and 23S rRNA.
For metagenomics, the riboPOOLs are available as combinational reagent, for example as Pan-prokaryote:Human mix, based on the expected ratios of your sample.
The DA-Cell Laminar wash technology replaces centrifugation by using a novel DA-Cell technology, which is gentle to cells, giving higher retention.
Removing ribosomal RNAs (rRNAs) to allow sensitive detection of scientifically relevant RNAs by Next Generation Sequencing, is currently performed with costly kits limited to well-studied species.
riboPOOLs present an affordable and flexible solution that gives scientists absolute freedom to deplete rRNAs or other custom RNAs from any species.
Composed of high complexity pools of optimally-designed biotinylated DNA probes, riboPOOLs even outperformed Ribo-Zero (Illumina), depleting ~10% more rRNA while leaving other RNA intact.
riboPOOLs are available for any species. Contact us for your specific needs.
riboPOOLs in stock: Human, Mouse, Planarian, Drosophila, Silkworm. Available in 2, 5 or 10 nmol (20, 50, 100 reactions). Custom scales on request.
Protocol is based on biotin-streptavidin chemistry with magnetic bead capture and removal.
Fluorescence staining of selected organelle
Down-stream experiments unaffected – non-toxic and biological
Easy and straightforward
The new Viromer Cytostain adds content at great convenience at low toxicity. With the mRNA encoding fluorescent fused protein expression, you will stain your targeted organelle of interest in living cells without impacting viability. Your flexibility for downstream experiments are therefore retained.
The Viromer Cytostain reagent is a Viromer nanoparticle, complexed to mRNAs encoding for fluorescent proteins. Thanks to the features of the Viromer particle, the mRNA is efficiently delivered into the cell cytosol and the protein is directly expressed.
Viromer is an efficient, non-toxic polymer which is used for transfection of both standard and hard-to-transfect cells. The team at Lipocalyx has extensive experience in the development of tools for cell transfection, including the transfection of mRNA.
Straightforward protocol; rehydrate and add to cells. Signal detachable in 6 hours.
The new Viromer formulation has developed for higher efficiencies and easier protocols. It is a versatile tool for non-toxic transfection of mRNA into a broad range of standard and challenging cells. mRNA transfection has several benefits, in particular when plasmid DNA delivery and uptake is inefficient due to natural defence mechanisms against foreign dsDNA, such as immune cells.
Speed: mRNA does not need to reach the nucleus for cellular action and translation occurs through a promoter-independent process and the desired protein is detectable as early as 6 h post-transfection.
Safety: No risk of genomic integration and transient expression avoids toxicity related to protein accumulation.
Productivity: As simple as in nature, mRNA instructs directly cells to produce proteins. With an optimized delivery, it is then possible to reach very high expression levels of any intracellular, transmembrane or excreted protein.
The new Viromer formulation has developed for higher efficiencies and easier protocols.
It is a versatile tool for non-toxic transfection of pDNA into a broad range of standard and challenging cells. Viromer Plasmid serves as a great option to electroporation.
Genome-editing using Cas9/gRNA ribonucleoprotein
Pre-formed RNP complex enables a direct action of the CRISPR system upon delivery. There is no need to pass through the transcription/translation cell machinery for expressing the Cas9 protein, and it skips the assembly step with the gRNA into the cytosol. It is then faster and safer!
Second, the cell rapidly clears Cas9/gRNA RNPs through protein degradation pathways.
This transient action provides a certain degree of control as it greatly increases the fidelity of the endonuclease (less off-target cleavage) and there is no risk of integration into the cell genome.
siPOOLs™ are innovative, complex siRNA pools which reduce false positives & false negatives in siRNA knockdown experiments.
Individual siRNAs or low complexity siRNA pools containing 3-4 siRNAs often hit multiple off-target genes and exhibit variable target gene knock-down. Short interfering RNA (siRNA) pools, siPOOLs are highly complex and defined pools of 30 siRNAs, each siRNA present at picomolar working concentrations.
Benefits:
dilutes the off-target signature of each siRNA, increasing on-target specificity
ensures co-operative knock-down of the target gene, producing more robust and reliable results.
Download the new TechNote:
Publication:
Optimise conditions based on the affinity to different chelating metal ions: Ni2+, Cu2+, Co2+ or Zn2+
The MagReSyn® NTA Screening Kit enables testing of all four alternatives
The MagReSyn® microparticles consist of nitrilotriacetic acid (NTA) residues with a strong metal-chelating property. MagReSyn® NTA is pre-chelated with nickel ions for affinity purification of histidine-tagged proteins. The product has been engineered for exceptional specificity, delivering highly pure target proteins. Since different types of His-tagged proteins may have varying affinities for a particular metal ion, we also offer a His-tagged protein purification screening kit (MagReSyn® NTA-KIT) containing MagReSyn® NTA chelated with 4 alternate divalent metal ions (Ni2+, Cu2+, Co2+, Zn2+) to identify the most suitable metal ion for optimal purification of your particular target protein. MagReSyn® NTA Copper, -Cobalt and -Zinc are currently available in 2
Thermostable Reverse Transcriptase blended with Ribonuclease Inhibitor for an efficient cDNA synthesis
High yields of full lengths transcripts up to 12-15 kb
cDNA synthesis from complex templates at up to 55°C
High sensitivity detection from 1 pg of total RNA template
Request a free sample:
Transfecting cells with mRNA greatly improves protein expression levels in immune cells that have innate defence mechanisms against foreign DNA. Being a natural component of the cytosol, mRNA will stay intact and create a productive translation process. Viromer® RED and Viromer® YELLOW transfection reagents are designed to work well with both mRNA and pDNA. No special, expensive transfection reagent is required!
Pre-formulated transfection complexes for use with either Viromer® RED or Viromer® YELLOW Includes both a GFP-encoding mRNA- and a pCMV-GFP plasmid transfection complex. A perfect tool to evaluate the optimal conditions for your cells!
Comparison of mRNA and pDNA transfection, using Start Positive Controls:
The Start Positive Controls are available in two formats based on the different transfection reagents Viromer RED and Viromer YELLOW. Both include the pDNA-GFP plasmid, as well as GFP-encoding mRNA.
Viromer RED is versatile for standard and challenging cells, whilst Viromer YELLOW can be optimal for specific cells. Please contact us if you are unsure which is best for you.
VR-BUNDLE-01, Viromer RED pDNA/mRNA-GFP controls
VY-BUNDLE-01, Viromer YELLOW pDNA/mRNA-GFP controls
Price: SEK 683.-; DKK 525.-; NOK 683.-; € 70.-
Place your order here:
Want to learn more about Viromer® Transfection Reagents from Lipocalyx?
Get a copy of the FactBook here:
Twice as concentrated than other stains, make StainIN™ GREEN and StainIN™ RED Nucleic Acid Stains much more economical. You get highly sensitive, and non-toxic detection of gels. Developed by the professionals at HighQu.
Replace your green dye with StainIN™ GREEN:
2X more stain for the same price
Blue LED or UV detection compatibility
4X more sensitive to EtBr
Unique emission pattern stains RNA and DNA in different colours (RNA in red, DNA in green)
Replace your red dye with StainIN™ RED:
2x more concentrated than other red dyes
2X more sensitive than EtBr
Time saving staining of gels
Much more safe than EtBr
Ordering information:
NAS0201 StainIN™ GREEN Nucleic Acid Stain, 1 ml, 20000X; SEK 1.097.-; DKK 857.-
NAS0101 StainIN™ RED Nucleic Acid Stain, 1 ml, 20000X; SEK 1.097.-; DKK 857.-
Place your order here:
Product information sheet:
StainIN™ GREEN: StainIN GREEN Product Sheet
StainIN™ RED: StainIN RED Product Sheet
HighQu 2017 Catalogue: HighQu Catalogue 2017
Article: GEN#022 volume 34 #4 pg 20-21
Use Viromer RED and Viromer YELLOW for pDNA and mRNA, Viromer BLUE and Viromer GREEN for siRNA and miRNA.
Order your Viromer transfection reagent here:
Optimising transfections in four steps. With Viromer reagents, delivery of the complex is effective and cells are treated gently.
In our new LabBook, you get access to recommendations for both adherent and suspension cells.
Optimisation guidelines are based on using the following four main parameters:
Amount of complex
Cell density & confluency
Viromer – RNA/DNA ratio
Incubation time
Get you copy of the LabBook here:
pDNA/mRNA: LabBook-Viromer-RED-YELLOW
siRNA/miRNA: LabBook-Viromer-BLUE GREEN
The new mastermix is not only great for achieving best data. It also includes an inert blue dye for improved sample visibility during handling and pipetting. The highly experienced team at HighQu have developed a range of great performing PCR reagents.
The mastermixes give you
qPCR on instruments calibrated for low or high ROX concentration
qPCR from gDNA, cDNA, viral DNA, low copy number genes
Universal – both standard and fast cycling
Easy protocols – minimum optimization
Excellent for GC or AT rich templates
Highest sensitivity, rapid extension, early Ct values; based on the small molecular inhibitor technology Hot Start PCR
Supplied with PCR Water to guarantee the best performance.
Data sheets, ORA™ SEE qPCR Green Mix with Low or High ROX content:
Ready to test the ORA™ SEE qPCR Green Mix?
MagReSyn offers high capacity and strong magnetic moment improves the speed of your scientific protocols.
High density functional groups in a hyper-porous polymer matrix enables a maximised binding capacity. The awarded technology also helps to reduce time thanks to the great magnetic features.
Ligands include NTA, TiO2, ZrO2, Streptavidin, Protein A/G, Amine, Carboxyl, Trypsin and Chymotrypsin.
Get the brochure here: ReSyn Bio LabLife Brochure
Free samples and application notes are available on request:
Instead of manual preparations, Viromer® ONE RED is an easy, individual and reliable new transfection reagent which brings industry standard into your lab.
Comparative data:
Relative transfection efficacy. The highest efficacy on each cell line was set to 100%. Standard conditions according to suppliers protocol (n=8).
Protocol here: transfection-protocol-Viromer-ONE-RED
Defining functional interactions during biogenesis of epithelial junctions
Erasmus et.al., Nat Commun. 2016
Extensive nuclear sphere generation in the human Alzheimer’s brain
Kolbe et. al., NeuroBiolAging, 2016
Hepatic Fgf21 Expression Is Repressed after Simvastatin Treatment in Mice.
Ziros et. al., PLoS One., 2016
Systemic RNA delivery to dendritic cells
exploitsantiviral defence for cancer immunotherapy.
Kranz et. al., Nature. 2016
Delta-Like Ligand 4 Modulates Liver Damage by Down-Regulating Chemokine Expression.
Shen et. al., Am J Pathol., 2016
Tumor suppressor BTG1 promotes PRMT1-mediated ATF4 function in response to cellular stress.
Yuniati et. al., Oncotarget, 2016
Drug Delivery Using Novel Biological and Synthetic Materials
Ito et. al., Biomed Res Int, 2015
The Comparative Utility of Viromer RED and Lipofectamine for Transient Gene Introduction into Glial Cells
Rao et.al., Hindawi Publishing Group, BioMed Research International, 2015
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