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  • Confocal micrograph of Bacillus subtilis. Bacillus subtilis is a Gram-positive, rod-shaped bacterium, commonly found in soil. Fluorescent proteins (TagRFP-T, sfGFP, TagBFP, mKate2 and mOrange2), time-lapse confocal microscopy and biophysical models are being used to understand the organization of bacterial biofilms.
  • Confocal micrograph of Bacillus subtilis. Bacillus subtilis is a Gram-positive, rod-shaped bacterium, commonly found in soil. Fluorescent proteins (TagRFP-T, sfGFP, TagBFP, mKate2 and mOrange2), time-lapse confocal microscopy and biophysical models are being used to understand the organization of bacterial biofilms.
  • Confocal micrograph of Bacillus subtilis. Bacillus subtilis is a Gram-positive, rod-shaped bacterium, commonly found in soil. Fluorescent proteins (TagRFP-T, sfGFP, TagBFP, mKate2 and mOrange2), time-lapse confocal microscopy and biophysical models are being used to understand the organization of bacterial biofilms.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, T cells (stained for CD3; red) dendritic cells (stained for MHC class II; green) and macrophages (stained for LYVE-1; blue with some cells showing a tinge of green) can be seen. Cell nuclei have been stained with DAPI (grey). This normal cellular architecture is grossly disrupted in diseased skin (see related images). X10 magnification. Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, blood vessels (string-like structures stained for CD31; red), lymphatic vessels (ribbon-like structures stained for LYVE-1; blue) and dendritic cells (stained for CD11c; green) can be seen. Macrophages (stained for LYVE-1; blue) are also present. This normal cellular architecture is grossly disrupted in diseased skin (see related images). X10 magnification. Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, T cells (stained for CD3; red) dendritic cells (stained for MHC class II; green) and macrophages (stained for LYVE-1; blue with some cells showing a tinge of green) can be seen. Cell nuclei have been stained with DAPI (grey). This normal cellular architecture is grossly disrupted in diseased skin (see related images). X20 magnification. Scale bar (white) represents 100 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, blood vessels (string-like structures stained for CD31; green), lymphatic vessels (ribbon-like structures stained for LYVE-1; blue) and T cells (stained for CD3; red) can be seen. T cells are only found around dermal blood vessels. Macrophages (stained for LYVE-1; blue) are also present. This normal cellular architecture is grossly disrupted in diseased skin (see related images). X10 magnification. Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels (string-like structures). A network of lymphatic vessels (ribbon-like structures) is also present. In this image, human skin lymphatic vessels (stained for LYVE-1; blue) and white blood cells comprised of dendritic cells (stained for CD11c; green) and T cells (stained for CD3; red) can be seen. Some macrophages also express the protein LYVE-1 similar to lymphatic vessel cells which can be appreciated as blue cells within and in between the sheaths of white blood cells. This normal cellular architecture is grossly disrupted in diseased skin (see related images). X10 magnification. Scale bar (white) represents 200 micrometres.
  • Papanicolaou stained smear of a clival chordoma, microscopy. Chordomas are cancers formed of cells which resemble those of the notochord (spine) of a developing foetus. Although they can present anywhere within the spine and skull, the majority grow in the sacral region of the spine, corresponding to the lower back. This image shows a Papanicolaou (Pap) stained smear obtained from a needle biopsy of a chordoma in the clivus, a part of the cranium at the base of the skull.
  • Cellular architecture of human skin lymphoma imaged by whole mount tissue microscopy. Normal human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In diseased skin, such as in skin lymphoma as seen here, this normal architecture becomes distorted. In this image, lots of T cells (stained for CD3; red), dendritic cells (stained for CD11c; green) and macrophages (stained for LYVE-1; blue) have infiltrated the skin. X20 magnification. Scale bar (white) represents 100 micrometres.
  • Papanicolaou stained smear of a C2 vertebral chordomal mass, microscopy. Chordomas are cancers formed of cells which resemble those of the notochord (spine) of a developing foetus. Although they can present anywhere within the spine and skull, the majority grow in the sacral region of the spine, corresponding to the lower back. This image shows a Papanicolaou (pap) stained smear obtained from a needle biopsy of a chordoma of the C2 vertebrae, located at the top of the neck just underneath the base of the skull.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. This image was taken greater than 150 micrometres beneath the junction that joins the dermal and epidermal layers of the skin (dermo-epidermal junction). At this level, dendritic cells (stained for CD11c; green) and macrophages (stained for LYVE-1; blue) form clusters around blood vessels (stained for CD31; red). This normal cellular architecture is grossly disrupted in diseased skin (see related images). Scale bar (white) represents 100 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. This image was taken directly beneath the junction that joins the dermal and epidermal layers of the skin (dermo-epidermal junction). At this level, the capillary network (stained for CD31; red) is visualised against a lawn of autofluorescent dermal papillae (finger-like projections of the dermis; green) scattered with dendritic cells (stained for CD11c; green) and macrophages (stained for LYVE-1; blue). This normal cellular architecture is grossly disrupted in diseased skin (see related images). Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. This image was taken less than 20 micrometres beneath the junction that joins the dermal and epidermal layers of the skin (dermo-epidermal junction). At this level, dendritic cells (stained for CD11c; green) form clusters around and between blood capillary loops (stained for CD31; red). The blind-ended tips of initial lymphatic vessels are just visible (stained for LYVE-1; blue) at this level. This normal cellular architecture is grossly disrupted in diseased skin (see related images). Scale bar (white) represents 200 micrometres.
  • Vitamin C (ascorbic acid) crystals imaged by cross polarised light microscopy. Vitamin C is an antioxidant and is important for collagen formation and wound healing. A good source of vitamin C is found in a variety of fruit and vegetables including citrus friuts, brussels sprouts and broccoli. It is a water soluble vitamin that cannot be stored in the body so needs to be ingested regularly. A lack of Vitamin C causes scurvy. 100X image magnification.
  • A. Donne & L. Foucault, Cours de Microscopie
  • A. Donne & L. Foucault, Cours de Microscopie
  • Cours de microscopie complémentaire des études médicales ... / par Al. Donné.
  • Cours de microscopie complémentaire des études médicales ... / par Al. Donné.
  • Cours de microscopie complémentaire des études médicales ... / par Al. Donné.
  • Cours de microscopie complémentaire des études médicales ... / par Al. Donné.
  • Cours de microscopie complémentaire des études médicales ... / par Al. Donné.
  • Journal of the Royal Microscopical Society.
  • Journal of the Royal Microscopical Society.
  • A practical treatise on the use of the microscope, including the different methods of preparing and examining animal, vegetable, and mineral structures / by John Quekett.
  • A practical treatise on the use of the microscope, including the different methods of preparing and examining animal, vegetable, and mineral structures / by John Quekett.
  • A practical treatise on the use of the microscope, including the different methods of preparing and examining animal, vegetable, and mineral structures / by John Quekett.
  • A practical treatise on the use of the microscope : including the different methods of preparing and examining animal, vegetable, and mineral structures / by John Quekett ; illustrated with eleven plates and upwards of three hundred wood engravings.
  • Martin Frobenius Ledermüllers ... [Vol. I.] Mikroskopische Gemüths- und Augen-Ergötzung: bestehend in ein hundert nach der Natur gezeichneten und mit farben erleuchteten Kupfertafeln, sammt deren Erklärung. [Vol. II] Nachlesse, etc. I[-V] Sammlung.--Abgenöthigte Vertheidigung; als ein Anhang seiner Mikroskopischen Gemüths- und Augen-Ergötzung: wider einige von dem ... Verfasser des Neuesten aus dem Reiche der Pflanzen [i.e. W.F. von Gleichen] ... geäuserte Zweifel und Vorwürfe. Nebst einer Beylage ... A.W. Winterschmidts, welche die Abbildung einer ... Stubenfliege, enthält / [Martin Frobenius Ledermüller].
  • Employment for the microscope ... I. An examination of salts and saline substances ... also ... considerations on gems, poisons ... and ... other subjects. II. An account of various animalcules ... and ... other ... discoveries ... Likewise a description of the microscope used / In two parts : illustrated with seventeen copper plates by Henry Baker.