Ds fi1 5 megapixel color camera

Manufactured by Nikon

Sourced in Azerbaijan

The DS-Fi1 is a 5-megapixel color camera designed for laboratory applications. It captures digital images with a resolution of 2560 x 1920 pixels.

Automatically generated - may contain errors

Lab products found in correlation

Nis elements software v4, by Nikon (4 mentions) Ti e inverted microscope, by Nikon (4 mentions) Las v3, by Leica (2 mentions) Mz10f stereomicroscope, by Leica (1 mentions) Az100 multizoom microscope, by Nikon (1 mentions) Fv3000 inverted confocal microscope, by Olympus (1 mentions) Fluoview software, by Olympus (1 mentions)

5 protocols using ds fi1 5 megapixel color camera

Stereoimaging Techniques for Tissue Analysis

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Stereoimages (brightfield and fluorescence) were captured with a Leica MZ10F stereomicroscope and the extended depth-of-focus feature of LAS v3.7 software (Leica Microsystems, Wetzlar, Germany). Brightfield and epifluorescence images of tissue sections were obtained using a Nikon Ti-E inverted microscope equipped with a DS-Fi1 5-megapixel color camera (Nikon Instruments), a CoolSNAP HQ2 14-bit monochrome camera (Photometrics, Tucson, AZ) and NIS Elements software v4.13 (Nikon Instruments).

Stewart M.D., Lopez S., Nagandla H., Soibam B., Benham A., Nguyen J., Valenzuela N., Wu H.J., Burns A.R., Rasmussen T.L., Tucker H.O, & Schwartz R.J. (2016). Mouse myofibers lacking the SMYD1 methyltransferase are susceptible to atrophy, internalization of nuclei and myofibrillar disarray. Disease Models & Mechanisms, 9(3), 347-359.

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Bacterial β-Glucuronidase Detection in Roots

Cited 1 time

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β-Glucuronidase expression by bacteria was detected by staining whole roots in X-Gluc buffer (1 mM 5-bromo-4-chloro-3-indolyl-β-d-glucuronic acid, cyclohexylammonium salt; 0.02% SDS, 50 mM Na-phosphate [pH 7]) (70 (link)) for 48 h. Whole roots were imaged on an AZ100 Multi-Zoom microscope equipped with a DS-Fi1, 5-megapixel color camera (Nikon Instruments, Melville, NY).

Mendis H.C., Madzima T.F., Queiroux C, & Jones K.M. (2016). Function of Succinoglycan Polysaccharide in Sinorhizobium meliloti Host Plant Invasion Depends on Succinylation, Not Molecular Weight. mBio, 7(3), e00606-16.

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Microscopy Imaging of Tissue Sections

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Brightfield and epifluorescence images of tissue sections were obtained using a Nikon Ti-E inverted microscope equipped with a DS-Fi1 5-megapixel color camera (Nikon Instruments), a CoolSNAP HQ2 14-bit monochrome camera (Photometrics, Tucson, AZ) and NIS Elements software v4.13 (Nikon Instruments). Stereoimages (brightfield and fluorescence) were captured with a Leica MZ10F stereomicroscope and the extended depth-of-focus feature of LAS v3.7 software (Leica Microsystems, Wetzlar, Germany).

Valenzuela N., Fan Q., Fa'ak F., Soibam B., Nagandla H., Liu Y., Schwartz R.J., McConnell B.K, & Stewart M.D. (2016). Cardiomyocyte-specific conditional knockout of the histone chaperone HIRA in mice results in hypertrophy, sarcolemmal damage and focal replacement fibrosis. Disease Models & Mechanisms, 9(3), 335-345.

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Cell Culture Imaging Protocol

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Brightfield and fluorescence images of cell cultures were acquired using a Nikon Ti-E inverted microscope attached with a DS-Fi 1 5-megapixel color camera (Nikon Instruments). Images were captured and analyzed using NIS Elements software v4.13 (Nikon Instruments).

Raghunathan S., Islas J.F., Mistretta B., Iyer D., Shi L., Gunaratne P.H., Ko G., Schwartz R.J, & McConnell B.K. (2019). Conversion of Human Cardiac Progenitor Cells into Cardiac Pacemaker-like Cells. Journal of molecular and cellular cardiology, 138, 12-22.

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Evaluating Purkinje-like Cell Differentiation

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To initially investigate the morphological changes, as well as expression of the CNTN2-mCherry tag introduced by CRISPR-Cas9 into the cells and determine if the cells have successfully differentiated into Purkinje-like cells, fluorescence microscopy was used. Brightfield and fluorescence images were taken using either a Nikon Ti-E inverted microscope attached with a DS-Fi 1 5-megapixel color camera (Nikon Instruments), or an FV3000 inverted confocal microscope (Olympus). NIS Elements software v4.13 (Nikon Instruments) or Fluoview Software (Olympus) were used to capture and analyze the images.

Prodan N., Ershad F., Reyes-Alcaraz A., Li L., Mistretta B., Gonzalez L., Rao Z., Yu C., Gunaratne P.H., Li N., Schwartz R.J, & McConnell B.K. (2022). Direct reprogramming of cardiomyocytes into cardiac Purkinje-like cells. iScience, 25(11), 105402.

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