Er 80 ccd

Manufactured by Philips

The ER-80 CCD is a laboratory equipment product from Philips. It is a Charge-Coupled Device (CCD) sensor used for image capture and detection applications. The ER-80 CCD provides high-resolution image data acquisition capabilities for scientific and industrial research purposes.

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Lab products found in correlation

Cm120 tem, by Philips (3 mentions)

3 protocols using er 80 ccd

Visualizing K18 and IAPP Protein Fibrils

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PFFs formed by K18 in the presence or absence of IAPP were visualized by negative stain TEM as described previously [24 ]. Tau PFFs and IAPP-tau PFFs were adsorbed to glow discharged 400 meshed carbon-coated copper grids for 2 min, quickly washed three times with Tris-HCl buffer (50 mM, pH 7.4), and floated upon two drops of 0.75% uranyl formate for 30 s. The grids were allowed to dry before imaging on a Phillips CM 120 TEM operating at 80 kV. The images were captured and digitized with an ER-80 CCD (8 megapixel) by advanced microscopy techniques.

Zhang G., Meng L., Wang Z., Peng Q., Chen G., Xiong J, & Zhang Z. (2022). Islet amyloid polypeptide cross-seeds tau and drives the neurofibrillary pathology in Alzheimer’s disease. Molecular Neurodegeneration, 17, 12.

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Negative Staining of Protein Samples

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Samples were adsorbed to glow discharged 400 mesh carbon coated copper grids (EMS) for 2 minutes. The grids were quickly transferred through three drops of Tris-HCl (50 mM pH 7.4) rinse, then floated upon two consecutive drops of 0.75% uranyl formate 30 seconds each. Stain was either aspirated or blotted off with #1 Whatman filter paper triangles. Grids were allowed to dry before imaging on a Phillips CM 120 TEM operating at 80 kV. Images were captured and digitized with an ER-80 CCD (8 megapixel) by advanced microscopy techniques.

Mao X., Ou M.T., Karuppagounder S.S., Kam T.I., Yin X., Xiong Y., Ge P., Umanah G.E., Brahmachari S., Shin J.H., Kang H.C., Zhang J., Xu J., Chen R., Park H., Andrabi S.A., Kang S.U., Gonçalves R.A., Liang Y., Zhang S., Qi C., Lam S., Keiler J.A., Tyson J., Kim D., Panicker N., Yun S.P., Workman C.J., Vignali D.A., Dawson V.L., Ko H.S, & Dawson T.M. (2016). Pathological α-synuclein transmission initiated by binding lymphocyte-activation gene 3. Science (New York, N.Y.), 353(6307), aah3374.

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Negative Staining of α-Synuclein Fibrils

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α-syn PFF or PAR-α-syn PFF were adsorbed to glow discharged 400 meshed carbon coated copper grids (Electron Microscopy Sciences, Hatfield, PA) for 2 min, quickly washed twice with Tris-HCl (50 mM, pH 7.4), and floated upon two drops of 0.75% uranyl formate for 30 s each. The grids were allowed to dry before imaging on a Phillips CM 120 TEM operating at 80 kV. The images were captured and digitized with an ER-80 CCD (8 megapixel) by advanced microscopy techniques.

Kam T.I., Mao X., Park H., Chou S.C., Karuppagounder S.S., Umanah G.E., Yun S.P., Brahmachari S., Panicker N., Chen R., Andrabi S.A., Qi C., Poirier G.G., Pletnikova O., Troncoso J.C., Bekris L.M., Leverenz J.B., Pantelyat A., Ko H.S., Rosenthal L.S., Dawson T.M, & Dawson V.L. (2018). Poly (ADP-ribose) Drives Pathologic α-Synuclein Neurodegeneration in Parkinson’s Disease.. Science (New York, N.Y.), 362(6414), eaat8407.

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