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Ix71 inverted microscope

Manufactured by PerkinElmer
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The IX71 inverted microscope is a high-performance optical system designed for a variety of laboratory applications. It features a stable and durable construction, providing consistent performance and reliable operation. The IX71 is equipped with advanced optics and illumination systems to enable clear and detailed imaging of samples.

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Lab products found in correlation

Cytation 5 cell imaging multi mode reader, by Agilent Technologies (2 mentions) Bx51 upright microscope, by Olympus (2 mentions) Openlab software, by PerkinElmer (2 mentions) Volocity, by PerkinElmer (2 mentions) Dm 1000 led, by Adobe (2 mentions) A1r gaasp inverted spconfocal microscope, by Nikon (2 mentions)

2 protocols using ix71 inverted microscope

1

Multimodal Microscopic Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Thin sections were imaged on an Olympus BX51 upright microscope and
cultured cells were imaged on an Olympus IX71 inverted microscope using Openlab
software (PerkinElmer). Chromogenic stains were imaged on a Leica DM 1000 LED.
Fiji50 (link) and/or
Photoshop (Adobe) were used to process (brightness, contrast and gamma) and
merge channels. Thick sections for 3D analysis of connectivity and clonal
analysis were imaged on a Leica upright AOBS confocal microscope and processed
and analyzed using Imaris (Bitplane) or Volocity (PerkinElmer) software. For
R26R-Confetti+/− mouse
and pSMAD3 analysis, images were acquired using a Nikon A1R GaAsP inverted SP
confocal microscope and NIS elements software and processed and analyzed using
Imaris software. Sirius-red-stained sections were imaged using a Cytation 5 cell
imaging multi-mode reader (BioTek).
Schaub J.R., Huppert K.A., Kurial S.N., Hsu B.Y., Cast A.E., Donnelly B., Karns R.A., Chen F., Rezvani M., Luu H.Y., Mattis A.N., Rougemont A.L., Rosenthal P., Huppert S.S, & Willenbring H. (2018). De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation. Nature, 557(7704), 247-251.
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2

Multimodal Microscopic Imaging Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Thin sections were imaged on an Olympus BX51 upright microscope and
cultured cells were imaged on an Olympus IX71 inverted microscope using Openlab
software (PerkinElmer). Chromogenic stains were imaged on a Leica DM 1000 LED.
Fiji50 (link) and/or
Photoshop (Adobe) were used to process (brightness, contrast and gamma) and
merge channels. Thick sections for 3D analysis of connectivity and clonal
analysis were imaged on a Leica upright AOBS confocal microscope and processed
and analyzed using Imaris (Bitplane) or Volocity (PerkinElmer) software. For
R26R-Confetti+/− mouse
and pSMAD3 analysis, images were acquired using a Nikon A1R GaAsP inverted SP
confocal microscope and NIS elements software and processed and analyzed using
Imaris software. Sirius-red-stained sections were imaged using a Cytation 5 cell
imaging multi-mode reader (BioTek).
Schaub J.R., Huppert K.A., Kurial S.N., Hsu B.Y., Cast A.E., Donnelly B., Karns R.A., Chen F., Rezvani M., Luu H.Y., Mattis A.N., Rougemont A.L., Rosenthal P., Huppert S.S, & Willenbring H. (2018). De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation. Nature, 557(7704), 247-251.
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