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Optimize yourlaser capture microdissection (LCM) experiments to get the best results. We’ve compiled a detailed knowledgebase of the top tips and tricks to meet your research needs.
View the relevant questions below:
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The ArcturusXT™ LCM Instrument has a proprietary combination of a gentle IR laser and a powerful UV laser that work in conjunction to efficiently isolate cells from frozen sections or paraffin embedded sections without changing morphology or integrity of the biological content. The IR laser helps to capture the cells of interest, and the UV laser microdissects the captured cells. This is done without affecting the morphology of the cells, and allows for visual inspection of the remaining specimen to help ensure the quality of the sample collected. In addition to the flexibility that the dual laser system provides, there is the flexibility of multiple stage inserts for various sample types. A wide-slide stage format is available for neurobiology researchers working with very large sections of brain tissue. The petri dish stage insert enables live-cell microdissection applications such as stem cell research and other rare-cell isolations.
First, optimize the visualization of the image in the live video at 2X by increasing or decreasing the brightness setting, then right-click on the overview image and select "remember settings". This resets your optimized image settings, and when you select "re-acquire overview image" you will now generate a perfectly exposed overview image.
Some other kits have been used for RNA isolation from LCM cells. These kits include the RecoverAll™ Total Nucleic Acid Isolation Kit for Formalin-Fixed Paraffin-Embedded (FFPE) (Cat. No. AM1975), RecoverAll™ Multi-Sample RNA/DNA Isolation Workflow (Cat. No. A26135), and the RNAqueous™- Micro Total RNA Isolation Kit (Cat. No. AM19310).
The Arcturus™ PicoPure™ DNA Extraction Kit (Cat. No. KIT0103) offers an easy, streamlined genomic extraction procedure that produces PCR-ready DNA. It allows you to extract and amplify DNA in the same tube, without organic extraction or spin columns, and to recover DNA from as few as 10 cells prepared by laser capture microdissection (LCM) or other tissues. The kit provides conveniently packaged, stable Proteinase K, PCR-compatible DNA Reconstitution Buffer and a complete user guide.
With this kit, you can amplify as little as 5 ng of RNA isolated from formalin-fixed, paraffin embedded (FFPE) tissues.
The Arcturus™ PicoPure™ RNA Isolation Kit removes total cellular RNA from pico-scale samples including frozen sections, alcohol fixed-, or fresh samples. Please note, samples fixed with formaldehyde are not recommended for use with this kit.
The dual-laser (IR) and UV nature of the ArcturusXT ™ Laser Capture Microdissection System offers ultimate flexibility for tissue preparation. A wide variety of tissues can be mounted on the system and subsequently microdissected off. We offer three types of slides that can be used for microdissection:
The cresyl violet stain is a hydrophilic, basic stain that binds to negatively charged nucleic acids. It is often used to identify target cells for LCM. If the tissue morphology has been damaged, cresyl violet might not clearly show cell distribution, and therefore acridine orange stain may provide better contrast between clusters of cells. Acridine orange is a fluorescent stain that intercalates with nucleic acids and can offer an advantage when microdissecting single cells as the cells will fluoresce on the cap after microdissection allowing for easy retrieval.
For recovery of miRNA from formalin-fixed samples, we recommend using RecoverAll™ Total Nucleic Acid Isolation Kit for FFPE. You can isolate total and miRNA using the RecoverAll™ Total Nucleic Acid Isolation Kit for FFPE, then use that prep for enrichment of miRNA using the enrichment protocol described in the instructions for the mirVana™ kit. For unfixed LCM samples, you could use an RNAqueous™ kit.
While we have not tested this in-house, there is evidence that it is possible to use tissues preserved in RNAlater™ Stabilization Solution and then perform laser capture microdissection. Please see the reference below:
Thelen P, Burfeind P, Grzmil M et al. (2004) cDNA microarray analysis with amplified RNA after isolation of intact cellular RNA from neoplastic and non-neoplastic prostate tissue separated by laser microdissections. Int J Oncol 24(5):1085-1092.
For Research Use Only. Not for use in diagnostic procedures.