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Red Hat Inc redhat linux workstations
Redhat Linux Workstations, supplied by Red Hat Inc, 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/redhat+linux+workstations/linux+redhat+workstation/pm30193229-66-19-19
Average 90 stars, based on 1 article reviews
redhat linux workstations - by Bioz Stars, 2026-11
90/100 stars

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Article Title: Homology modelling of human divalent metal transporter (DMT): Molecular docking and dynamic simulations for duodenal iron transport.
Article Snippet: Iron transport through the duodenum is regulated by carrier proteins, one of which 26 is the ubiquitously distributed divalent metal transporter (DMT1) which is responsible for the 27 uptake of iron across the apical surface of the duodenal enterocyte.. The crystallographic structure 28 of Staphylococcus capitis divalent metal ion transporter (ScaDMT1) was obtained and it was 29 used as a template for the construction of a homology model of human divalent metal transporter 30 (hDMT1).. The binding site for hDMT1 was determined by using SiteMap as well as molecular 31 docking studies on ScaDMT1.



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Longitudinal image of villi to demonstrate the localization of the antimicrobial SBD-3 (red) in the epithelial cells of the small intestine. Blue (DAPI) indicates cell nuclei and green (Phallicidin) shows F-actin. Note the green microvillous, brush border on the apical side of the cells (magnification ×200; <t>deconvolution</t> via 5 iterations). Panel A is magnification ×1200, Panel B is magnification ×500, and Panel C is magnification ×500. White arrows indicate SBD-3 in the epithelium and subepithelial capillaries in the panel A and are associated with the lacteal and surrounding capillaries in panel C. Scale bar in panel B = 90 microns.
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Longitudinal image of villi to demonstrate the localization of the antimicrobial SBD-3 (red) in the epithelial cells of the small intestine. Blue (DAPI) indicates cell nuclei and green (Phallicidin) shows F-actin. Note the green microvillous, brush border on the apical side of the cells (magnification ×200; <t>deconvolution</t> via 5 iterations). Panel A is magnification ×1200, Panel B is magnification ×500, and Panel C is magnification ×500. White arrows indicate SBD-3 in the epithelium and subepithelial capillaries in the panel A and are associated with the lacteal and surrounding capillaries in panel C. Scale bar in panel B = 90 microns.
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Longitudinal image of villi to demonstrate the localization of the antimicrobial SBD-3 (red) in the epithelial cells of the small intestine. Blue (DAPI) indicates cell nuclei and green (Phallicidin) shows F-actin. Note the green microvillous, brush border on the apical side of the cells (magnification ×200; <t>deconvolution</t> via 5 iterations). Panel A is magnification ×1200, Panel B is magnification ×500, and Panel C is magnification ×500. White arrows indicate SBD-3 in the epithelium and subepithelial capillaries in the panel A and are associated with the lacteal and surrounding capillaries in panel C. Scale bar in panel B = 90 microns.
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Longitudinal image of villi to demonstrate the localization of the antimicrobial SBD-3 (red) in the epithelial cells of the small intestine. Blue (DAPI) indicates cell nuclei and green (Phallicidin) shows F-actin. Note the green microvillous, brush border on the apical side of the cells (magnification ×200; <t>deconvolution</t> via 5 iterations). Panel A is magnification ×1200, Panel B is magnification ×500, and Panel C is magnification ×500. White arrows indicate SBD-3 in the epithelium and subepithelial capillaries in the panel A and are associated with the lacteal and surrounding capillaries in panel C. Scale bar in panel B = 90 microns.
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Longitudinal image of villi to demonstrate the localization of the antimicrobial SBD-3 (red) in the epithelial cells of the small intestine. Blue (DAPI) indicates cell nuclei and green (Phallicidin) shows F-actin. Note the green microvillous, brush border on the apical side of the cells (magnification ×200; deconvolution via 5 iterations). Panel A is magnification ×1200, Panel B is magnification ×500, and Panel C is magnification ×500. White arrows indicate SBD-3 in the epithelium and subepithelial capillaries in the panel A and are associated with the lacteal and surrounding capillaries in panel C. Scale bar in panel B = 90 microns.

Journal: Eplasty

Article Title: Upregulation of Defensins in Burn Sheep Small Intestine

doi:

Figure Lengend Snippet: Longitudinal image of villi to demonstrate the localization of the antimicrobial SBD-3 (red) in the epithelial cells of the small intestine. Blue (DAPI) indicates cell nuclei and green (Phallicidin) shows F-actin. Note the green microvillous, brush border on the apical side of the cells (magnification ×200; deconvolution via 5 iterations). Panel A is magnification ×1200, Panel B is magnification ×500, and Panel C is magnification ×500. White arrows indicate SBD-3 in the epithelium and subepithelial capillaries in the panel A and are associated with the lacteal and surrounding capillaries in panel C. Scale bar in panel B = 90 microns.

Article Snippet: Deconvolution and image analysis were performed by transferring the data sets to a Linux/RedHat workstation employing SoftWoRx software (Applied Precision), which uses an algorithm experimentally produced on the system from the convolution of a point spread function (PSF) to differentiate and reduce extraneous light or scattered light captured by the camera.

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