double-helix microswimmer array (Double Helix)
Structured Review

Double Helix Microswimmer Array, supplied by Double Helix, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/double-helix+array/pmc08442928-58-3-3?v=Double+Helix
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "3D printed personalized magnetic micromachines from patient blood–derived biomaterials"
Article Title: 3D printed personalized magnetic micromachines from patient blood–derived biomaterials
Journal: Science Advances
doi: 10.1126/sciadv.abh0273
Figure Legend Snippet: ( A ) A color-coded assignment of the systematically varied laser intensities for the fabrication of albumin microswimmer. ( B ) The structural quality of the 3D printed albumin microswimmers assessed with differential interference contrast (DIC) imaging. ( C ) The length of the microswimmers measured as a function of the applied laser intensity. ( D and E ) DIC and fluorescence images of the 3D printed albumin-based micromachines. ( F ) Fabrication strategy of the mouse plasma micromachines. ( G ) DIC and fluorescence images of the 3D printed plasma and platelet lysate microswimmers.
Techniques Used: Imaging, Fluorescence, Clinical Proteomics
Figure Legend Snippet: Swimming trajectories and step-out frequencies of albumin microswimmers with varying designs: ( A ) A single-helix microswimmer, ( B ) double-helix microswimmer, and ( C ) microroller. The step-out frequencies are determined by stepwise increasing the actuation frequency.
Techniques Used:
Figure Legend Snippet: ( A ) Enzymatic degradation observed under the time-lapse DIC imaging in the presence of trypsin enzyme at a concentration comparable to the pancreatic juice at 37°C. ( B ) An increase in the dimensions of albumin microswimmers during the degradation before the total collapse of the microswimmer fabric. ( C and D ) The biocompatibility of the degradation products of albumin microswimmers assessed by the viability of the exposed haMSCs at 24 hours. (C) Representative calcein acetoxymethyl ester/ethidium homodimer-1–stained fluorescence images of the exposed haMSCs. (D) The viability of the exposed haMSCs assessed based on the quantified intracellular adenosine 5′-triphosphate amount.
Techniques Used: Imaging, Concentration Assay, Staining, Fluorescence