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\r\n\r\n\r\nMode, and then Grayscale. Go to the Channels window and click the New Spot Channel icon. A new spot channel is created. Select the name depending on the RIP you will be using.\r\n\r\nSelect the original channel and invert it by selecting Image > Adjustments, and then Invert. Select and copy the entire image to the new channel. Go back to the original channel and delete all of its contents (select all > delete). Save the file as a TIFF with Spot Colors selected.\r\n\r\n\r\n\r\n\r\n\t
\r\n\r\n\r\nHere you can access the full White Ink Workflow Guide for the HP Latex 700W, 800W, and R Series Printers.", "author": "@type": "Person", "name": "HP Daniela Ciolompea" , "image": "https:\/\/lkc.hp.com\/storage\/app\/uploads\/public\/630\/09d\/d1e\/63009dd1e9ed0009306247.png"} function trackShare(event, link, network, type) var pagePath = ' -latex-white-ink-workflow-designing-adobe-photoshop'; var opt_target = '[' + type + '] (883) HP Latex white ink workflow - Designing in Adobe Photoshop '; if (window.ga) ga('send', 'social', network, 'Share', opt_target, 'page': pagePath ); function onLiked(data) $("#likes").html(" " + data.likes + "") Blog HP Latex white ink workflow - Designing in Adobe Photoshop Print Google translate HP Latex white ink workflow - Designing in Adobe Photoshop HP Daniela Ciolompea 5th of September 2022 #Ink
Creating a white Spot channel
Methods: Four groups of Japanese white rabbits underwent either PBOO by mild ligation of the urethra (2- and 4-week PBOO) or no obstruction (2- and 4-week sham). Histopathological examination was performed by Elastica van Gieson staining, scanning electron microscopy, transmission electron microscopy, and ultra-high voltage electron microscopy. The number of pixels representing elastin fibers in computerized images was analyzed using Adobe Photoshop Version 2.0.
A, coronal images of a VX-2 tumor-bearing rabbit. A focus of intense FDG uptake was observed in the left lobe of the liver on FDG-PET (black arrow) and fused PET/CT (white arrow) images. CT exhibited a low attenuation area in the corresponding region (white arrow). Heart/vascular structure and intestine showed high FDG uptake on FDG-PET and fused PET/CT images (expressed as H, V, and I, respectively, on PET). Left: contrast-enhanced CT; middle: FDG-PET, and right: fused PET/CT image. B, transaxial high-resolution images of the rabbit at the level of the primary tumor. Intense FDG uptake was observed in the left lobe of the liver on FDG-PET (black arrow) and fused PET/CT (white arrow) images. CT depicted a low attenuation area with inhomogeneous faint contrast enhancement in the corresponding region (white arrow). The macroscopic specimen demonstrated a solid tumor. G (low attenuation area): gall bladder. Top left: contrast-enhanced CT; top right: FDG-PET; bottom left: fused PET/CT; and bottom right: macroscopic tumor image of tumor removed from liver. C, transaxial high-resolution images of the rabbit at the level of the metastatic VX-2 tumor. A small focus of intense FDG uptake is seen in the abdominal wall on FDG-PET (black arrow) and the fused PET/CT (white arrow) images. CT revealed that this focal tracer uptake was corresponded to a 7-mm diameter metastatic lesion. A known granuloma (G) associated with the tumor implantation procedure was also seen clearly on CT. Note that only mild to moderate FDG uptake was observed in the marginal area of this granuloma in contrast to the intense FDG uptake in the small metastatic lesion. Top left: contrast-enhanced CT; top right: FDG-PET; and bottom right: fused PET/CT image.
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