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Lsm 510 meta laser scanning confocal microscopy

Manufactured by Nikon
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Sourced in Japan

The LSM 510 META Laser Scanning Confocal Microscopy is a high-performance imaging system designed for advanced microscopy applications. It utilizes laser scanning technology to produce high-resolution, optical sectioning images of samples. The system is capable of capturing detailed, three-dimensional information about the internal structure of specimens.

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Lab products found in correlation

Cell light edu apollo dna in vitro kit, by RiboBio (2 mentions)

Spelling variants of this product

Confocal microscopy (126 citations) Confocal laser scanning microscopy (87 citations) Laser confocal microscopy (22 citations) LSM 510 (16 citations) LSM 510 META (6 citations)

2 protocols using lsm 510 meta laser scanning confocal microscopy

1

Cell Proliferation Measurement Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell proliferation was also estimated using Cell-Light Edu Apollo DNA in vitro Kit (RiboBio, Guangzhou, China). Proliferative cells were visualized and imaged using a Zeiss LSM 510 META Laser Scanning Confocal Microscopy (Nikon, Tokyo, Japan). Proliferative cells were counted in different optical fields (magnification × 200) selected in a random manner and analyzed by the software of Image J.
Zhang L., Cao R., Li D., Sun Y., Zhang J., Wang X., Khan A., Liu Z., Niu B., Xu J, & Xie J. (2021). Ethionine-mediated reduction of S-adenosylmethionine is responsible for the neural tube defects in the developing mouse embryo-mediated m6A modification and is involved in neural tube defects via modulating Wnt/β-catenin signaling pathway. Epigenetics & Chromatin, 14, 52.
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2

Cell Proliferation Assay Using Confocal Microscopy

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Cell proliferation was also estimated using Cell-Light Edu Apollo DNA in vitro Kit (RiboBio, Guangzhou, China). Proliferative cells were visualized and imaged using a Zeiss LSM 510 META Laser Scanning Confocal Microscopy (Nikon, Tokyo, Japan). Proliferative cells were counted in different optical elds (magni cation ×200) selected in a random manner and analyzed by the software of Image J.
Zhang L., Cao R., Li D., Sun Y., Zhang J., Wang X., Khan A., Liu Z., Niu B., Xu J., & Xie J. (2021). METTL3-Mediated m6A Modification is Involved in Neural Tube Defects via Modulating Wnt/β-Catenin Signaling Pathway.
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