Electroosmotic (EO) pumps (also known as electrokinetic pumps) generate fluid flow and pressure in a compact system with no moving parts. They can be combined with microchannel heat exchangers to provide cooling for microelectronics. Researchers in Dr.
Researchers in Dr. Or Gozani's laboratory have produced lysine methyltransferases, histone octomers, purified nucleosomes, and antibodies for use in chromatin and epigenetic research.
Researchers in Dr. Roeland Nusse's laboratory have generated an Axin2CreERT2 knock-in mouse strain that can be used to identify and map stem cells in any tissue. The Wnt/β-catenin signaling pathway is instrumental for stem cell maintenance in multiple tissues.
Engineers in the Stanford Microfluidics Laboratory have developed a sensitive, high-resolution, label-free detection method for identifying and quantifying analytes on chip-based electrophoretic assays.
Hemizygous mice are viable and fertile with no anatomic abnormalities. Transgene expression is observed in aorta, heart, and brain. Transgenicdimethylarginine dimethylaminohydrolase (DDAH) activity is reflected in a reduction of plasma asymmetric dimethylarginine (ADMA).
Researchers in Prof. Juan Santiago's laboratory have developed a novel isotachophoresis (ITP) method to easily and seamlessly integrate various electrophoresis-based detection techniques with ITP preconcentration.
Stanford researchers have developed a versatile computational approach for easily visualizing and analyzing multidimensional molecular data, such as flow cytometry data.
We have recently shown that rab9 plays a key role in the transport of proteins between late endosomes and the trans Golgi network. Purified, recombinant, rab9 protein stimulated transport in a cell free system that reconstitutes this event.
RNKp30 monoclonal antibodies were generated by immunizing BALB/c mice with rNKp30-Fc fusion protein. The rNKp30-Fc fusion protein is a soluble protein consisting of the extracellular domain of rNKp30 fused to the Fc domain of human IgG1.
Researchers in Prof. Liqun Luo's laboratory have developed a mouse model system for in vivo, non-invasive, spatially- and temporally-controlled labeling of individual synapses.
The Light Field Microscopy (“LFM”) is a patented system that enables rapid acquisition of images to be virtually analyzed at any time in the future from different viewpoints or focus adjustments.
Researchers from Prof. Annelise Barron's laboratory have developed a novel method for purifying large, biologically produced protein polymers for DNA sequencing and genotyping.