Zebrafish embryo brain development, CFP, YFP, mCherry imaged at 860 nm and 1041 nm with InSight® DS+™.
Courtesy of Dr. Nadine Peyrieras, CNRS, Gif sur Yvette, France and LaVision Biotec

Maximum intensity projection of zebrafish embryo development, taken from both sides over 8 hours; imaged with InSight DS+.
Courtesy of Dr. Nadine Peyrieras, CNRS, Gif sur Yvette, France and LaVision Biotec

Z-stack of transgenic zebrafish larvae, labeled with GFP and CFP; imaged with Mai Tai® DeepSee™.
Courtesy of Dr. Rachel Wong, University of Washington, Seattle

Transgenic zebrafish embryo retina, revealing various neuronal cell types, imaged at 927 nm and 1041 nm with InSight DS+.
Courtesy of Dr. Xana Almeida, University of Cambridge, UK

Lymph vessel; imaged with InSight® DS+™.
Courtesy of Dr. Cameron Newell, Monash, University, Melbourne, Australia

Continuous tracking of T cells (tagged with CMPTX, imaged at 1080 nm) and dendritic cells
(tagged with GFP, imaged at 925 nm) interacting in mouse skin over several hours; imaged with InSight DS+.
Courtesy of Dr. Michael Kuligowski, Centenary Institute of Cancer Research and Cell Biology, Sydney, Australia

Continuous tracking of T cells (tagged with CMPTX, imaged at 1080 nm) and dendritic cells
(tagged with GFP, imaged at 925 nm) interacting in mouse skin over several hours; imaged with InSight DS+.
Courtesy of Dr. Michael Kuligowski, Centenary Institute of Cancer Research and Cell Biology, Sydney, Australia

Mouse ear, showing collagen (blue) and GFP labelled T cells (green); imaged with Mai Tai® DeepSee™.
Courtesy of Dr. Claudio Vinegoni, Mass General Hospital, Harvard University

Retinal ganglion cell; imaged with Mai Tai.
Courtesy of Dr. Gregory Schwartz, Northwestern University

Chemically cleared mouse heart total depth of 3.5 mm; imaged with Mai Tai DeepSee.
Courtesy of Mayandi Sivaguru, University of Illinois Urbana Champaign and Sakthivel Sadayappan, Loyola University, Chicago

Human meibomian gland, CARS imaging the lipid rich meibocytes and SHG visualizing the surrounding collagen;
acquired with InSight® DS+™.
Courtesy of Dr. Eric Potma, UC Irvine

SRS image of fatty liver, pump 802 nm and Stokes at 1040 nm; acquired with InSight DS+.
Courtesy of Dr. Ji-XIn Cheng, Purdue University

SRS image of spinal cord, pump 802 nm and Stokes at 1040 nm; acquired with InSight DS+.
Courtesy of Dr. Ji-XIn Cheng, Purdue University

CARS Z-stack of C.Elegans worm, visualizing lipids 19.
Courtesy of Dr. Daewon Moon and Dr. Hyunmin Kim, DGIST Daegu Gyeongbuk Institute of Science and Technology (DGIST)

CARS and MPEF imaging of C. Elegans, neuron cells labelled with GFP, lipid droplets revealed with CARS.
Courtesy of Dr. Daewon Moon and Dr. Hyunmin Kim, DGIST Daegu Gyeongbuk Institute of Science and Technology (DGIST)

Zebrafish embryo (6 hours post fertilization) using label free THG at 1140 nm; imaged with InSight® DS+™.
Courtesy of Dr. Nadine Peyrieras, CNRS, Gif sur Yvette, France

Mouse blood vessel wall, SHG and multiphoton excited fluorescence imaging with HighQ-2™.
Courtesy of Dr. Marc van Zandvoort, Maastrich University

Mouse mammary gland, label free image of collagen (SHG, magenta) and adipocytes (THG, yellow), imaged with InSight DS+™.
Courtesy of Dr. Marie Irondelle, Institut Curie/CNRS, Paris, France

3D images from a mouse brain cerebellum extending 1 mm deep into the tissue acquired via 3PF (left)
and THG (right) microscopy at 1.3 μm using a Spirit laser with a Spirit-NOPA.
Courtesy of Chris Xu, with permission from SPIE Publications: Wang, et. al., “In vivo three-photon
imaging of deep cerebellum,” Proc. SPIE:  Multiphoton Microscopy in the Biomedical Sciences
XVIII, vol. 10498, 2018.

Mouse kidney, with CARS (red), SHG (blue) and autofluorescence (green); imaged with Mai Tai® HP plus Inspire™ OPO.
Courtesy of Dr. Eric Potma, UC Irvine, CA

C. elegans, with CARS mapping out lipid rich areas and two-photon excited fluorescence from GFP and dsRed;
imaged with InSight® DS+™.
Courtesy of Dr. Eric Potma, UC Irvine, CA