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JenLab GmbH multiphoton microscopy (mpm)
Multiphoton Microscopy (Mpm), supplied by JenLab GmbH, 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/multiphoton+microscopy+(mpm)/multiphoton+microscopy/pm25810241-14-46-38
Average 90 stars, based on 1 article reviews
multiphoton microscopy (mpm) - by Bioz Stars, 2026-10
90/100 stars

Images

Related Articles

In Vivo:


Article Title: A case of photodistributed multicentric reticulohistiocytosis: correlation with multiphoton microscopy imaging.
Article Snippet: A multiphoton microscopy (MPM) tomograph (MPTflex; JenLab GmbH, Germany) was utilized to image one of the patient’s skin lesions.

Microscopy:


Article Title: A case of photodistributed multicentric reticulohistiocytosis: correlation with multiphoton microscopy imaging.
Article Snippet: A multiphoton microscopy (MPM) tomograph (MPTflex; JenLab GmbH, Germany) was utilized to image one of the patient’s skin lesions.

Imaging:


Article Title: A case of photodistributed multicentric reticulohistiocytosis: correlation with multiphoton microscopy imaging.
Article Snippet: A multiphoton microscopy (MPM) tomograph (MPTflex; JenLab GmbH, Germany) was utilized to image one of the patient’s skin lesions.

In Vivo Imaging:


Article Title: A case of photodistributed multicentric reticulohistiocytosis: correlation with multiphoton microscopy imaging.
Article Snippet: A multiphoton microscopy (MPM) tomograph (MPTflex; JenLab GmbH, Germany) was utilized to image one of the patient’s skin lesions.



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Graphical abstract of experimental design for imaging intravital C’Dot uptake and clearance in bone with 2-photon <t>microscopy.</t> A) Bone and osteocytes were exposed to fluorescent nanoparticles through a local subcutaneous injection above the third metatarsal (MT3) bone in a mouse hind paw. After C’Dot incubation, the MT3 was surgically isolated and secured for <t>multiphoton</t> imaging. B-D) Example images of C’Dots in the lacuno-canalicular network are shown. E-F) The high resolution of our imaging system enables subcellular localization. G) A short C’Dot incubation time and high frame averaging allows visualization of the canalicular network. H) Images can be analyzed for clearance kinetics of nanoparticle signal (from previous paper ) as well as subcellular distribution of signal. Scale bars = 10 μm.
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Image Search Results


Graphical abstract of experimental design for imaging intravital C’Dot uptake and clearance in bone with 2-photon microscopy. A) Bone and osteocytes were exposed to fluorescent nanoparticles through a local subcutaneous injection above the third metatarsal (MT3) bone in a mouse hind paw. After C’Dot incubation, the MT3 was surgically isolated and secured for multiphoton imaging. B-D) Example images of C’Dots in the lacuno-canalicular network are shown. E-F) The high resolution of our imaging system enables subcellular localization. G) A short C’Dot incubation time and high frame averaging allows visualization of the canalicular network. H) Images can be analyzed for clearance kinetics of nanoparticle signal (from previous paper ) as well as subcellular distribution of signal. Scale bars = 10 μm.

Journal: Scientific Reports

Article Title: Real-time visualization and modulation of endocytic dynamics in osteocytes in vivo

doi: 10.1038/s41598-025-05735-1

Figure Lengend Snippet: Graphical abstract of experimental design for imaging intravital C’Dot uptake and clearance in bone with 2-photon microscopy. A) Bone and osteocytes were exposed to fluorescent nanoparticles through a local subcutaneous injection above the third metatarsal (MT3) bone in a mouse hind paw. After C’Dot incubation, the MT3 was surgically isolated and secured for multiphoton imaging. B-D) Example images of C’Dots in the lacuno-canalicular network are shown. E-F) The high resolution of our imaging system enables subcellular localization. G) A short C’Dot incubation time and high frame averaging allows visualization of the canalicular network. H) Images can be analyzed for clearance kinetics of nanoparticle signal (from previous paper ) as well as subcellular distribution of signal. Scale bars = 10 μm.

Article Snippet: Fluorescent signal inside the functionally isolated MT3 was visualized with multiphoton microscopy (MPM) (Bergamo II, Thorlabs) as previously described .

Techniques: Imaging, Microscopy, Injection, Incubation, Isolation