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Application suite las v4

Manufactured by Leica

Leica Application Suite LAS V4.0 is a software suite that provides a comprehensive platform for the acquisition, processing, and analysis of images and data from Leica microscopes and imaging systems. It offers a user-friendly interface and a range of tools for image capture, annotation, measurements, and analysis.

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2 protocols using application suite las v4

1

Immunohistochemical Analysis of Tissue Samples

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The serial slices used for histopathological analysis were immunostained with polyclonal rabbit anti-human CD3 (Dako, 1:100), polyclonal rabbit anti-human CD20 (Thermo Fisher, 1:100), monoclonal mouse anti-human MHCII (Dako, 1:40), monoclonal mouse anti-human Ki67 (Dako, 1:10), and monoclonal rabbit anti-human vWF (Dako; 1:3200) antibodies. Immunolabeling was achieved with a high-sensitive horseradish spell out (PO) mouse or rabbit diaminobenzidine kit, with blocking of endogenous PO (Envision DAB+kit; Dako) in an autoimmunostainer (Cytomation S/N S38–7410-01; Dako). An antibody diluent (Dako), with background-reducing components was used to block hydrophobic interactions. The average of three fields from each slice was used to quantitatively evaluate different immunohistological parameters and all measurements were performed with a computer-based program (Leica microscope DM LB2 with Leica Application Suite LAS V4.0) using 20× magnification.
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2

Anatomical Analysis of Bamboo Leaf Blades

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For the woody bamboos, mature leaf blades were taken from the branches at the mid-culm, whereas for the herbaceous bamboos mature leaves were taken from the third node from the base. Fresh plant material was fixed in FAA 50 (Johansen, 1940) and later stored in 70% ethanol. Found on leaves of Arthrostylidiinae species, the green stripe was excluded from this work due to its anatomical peculiarities in relation to the remainder of the leaf blade (Judziewicz et al., 1999) .
Samples from the middle portion of the leaf blade were embedded in polyethylene glycol 1500 solution (adapted from Richter, 1985) (link) and cross-sectioned with a rotary microtome. Sections were cleared in sodium hypochlorite 50%, washed in distilled water, stained with Astra blue and Safranin (Bukatsh, 1972) , and finally mounted on semi-permanent slides with glycerol. Also, a maceration technique was performed by the Jeffrey's method (Johansen, 1940) in order to describe the epidermal features.
Descriptions were primarily based on Ellis (1976 (link)Ellis ( , 1979)) (link), and optical images were obtained on a Leica DM4000B microscope using the software Leica Application Suite LASV4.0.
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