C7070 digital camera

Manufactured by Olympus

Sourced in Japan

The Olympus C7070 is a digital camera designed for laboratory and scientific applications. It features a 7.1 megapixel CCD sensor and supports image capture in a variety of formats, including TIFF, JPEG, and RAW. The camera is capable of recording images and videos at resolutions up to 3072 x 2304 pixels.

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Lab products found in correlation

M205c stereomicroscope, by Leica (1 mentions) Quanta 450 environmental scanning electron microscope, by Thermo Fisher Scientific (1 mentions) E cadherin, by Agilent Technologies (1 mentions)

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Digital camera (379 citations) C7070 wide zoom digital camera (12 citations) C7070 zoom digital camera (4 citations)

4 protocols using c7070 digital camera

Stereomicroscopic Examination and Imaging of Arachnid Genitalia

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All specimens were examined and measured using a LEICA M205 C stereomicroscope. The bodies, male palps, and receptacles were photographed using an Olympus C7070 digital camera. Images were combined using Helicon Focus version 6.7.1 image stacking software (http://www.heliconsoft.com). Endogynes were removed and treated in lactic acid before photographing. All measurements are given in millimeters. Leg measurements are shown as: total length (femur, patella, tibia, metatarsus, tarsus). The left palpi of males were photographed using an FEI Quanta 450 Environmental Scanning Electron Microscope. The following abbreviations are used in the text and figures:
CA cymbial apophysis;
Em embolus;
Re receptacle;
REC the ratio of embolus length (green line in Fig. 1D) and cymbium length (blue line in Fig. 1D);
SR spiral ridge of embolus.
All specimens treated here are deposited in the Institute of Zoology, Chinese Academy of Sciences (IZCAS), Beijing, China.

Zhao H., Dinh-Sac P., Song Y., Do T.D, & Li S. (2018). Seven new species of Pinelema from Vietnam (Araneae, Telemidae). ZooKeys.

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Quantifying GstD1-GFP Expression in Drosophila

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In this experiment, the D. melanogaster transgenic line with GstD1-GFP reporter was used. The line was kindly provided by Dr. Tower (University of Southern California, Los Angeles, CA, United States).
To measure GstD1-GFP reporter expression, flies were anesthetized and photographed using a fluorescent microscope “MICMED-2 var.11” (LOMO, Russia) and video systems based on the Olympus C7070 digital camera (Olympus, Japan) on the 10th and 30th days of flavonoid consumption. The corrected total cell fluorescence (CTCF) was calculated using ImageJ software (National Institutes of Health, United States) as described elsewhere (Cali et al., 2015 (link)). The same assay was performed on flies treated for 12 h with 20 mM paraquat (Methyl Viologen, Sigma) in 5% sucrose (0.2 mL per vial). For each experimental group 10 flies were used.

Lashmanova E., Zemskaya N., Proshkina E., Kudryavtseva A., Volosnikova M., Marusich E., Leonov S., Zhavoronkov A, & Moskalev A. (2017). The Evaluation of Geroprotective Effects of Selected Flavonoids in Drosophila melanogaster and Caenorhabditis elegans. Frontiers in Pharmacology, 8, 884.

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Thermal Analysis of SIM Compounds

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HSM was carried out using an Olympus BX51 (Olympus Optical Co. Ltd., Tokyo, Japan) polarizing optical microscope equipped with a Linkam LTS350 hot stage (Linkam Scientific Instruments Ltd., Surrey England) and Linkam TMS94 programmable temperature controller. SIM API or SDP were placed on a glass slide and gradually heated at 5°C/min until 200°C. Photographs were taken at RT and near the melting point of SIM, using Olympus C-7070 Digital Camera (7.1 megapixel, 4× optical zoom).

Pabari R.M., Jamil A., Kelly J.G, & Ramtoola Z. (2014). Fast disintegrating crystalline solid dispersions of simvastatin for incorporation into orodispersible tablets. International Journal of Pharmaceutical Investigation, 4(2), 51-59.

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Histopathological Analysis of Apremilast Actinic Prurigo

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This descriptive study included paraffin-embedded tissues (from lip and skin incisional biopsy) in patients with a confirmed diagnosis of AP (n = 24). Two dermatopathologists who were experts in this area assessed all cases. Hematoxylin and eosin staining was used to analyze the histopathological characteristics of the samples, obtained from the patient. Sociodemographic data, such as age, sex, and biopsy site, were collected. Two micron sections were performed and stained by immunohistochemistry (monoclonal primary antibodies: Dako syndecan-1 (CD-138), clone: Ml15, 1:100 dilution; Dako E-cadherin, clone: NCH-38, 1:100 Ki-67, Dako, clone: MIB 1, 1:50 dilution; and MCM3, Abcam Cambridge UK, clone: ab97282, 1:100 dilution were used); the tissues were counterstained with Mayer's hematoxylin.
Expression was evaluated semi-quantitatively in five fields per case at ×400 [Table 1] and was photographed with an Olympus C-7070 digital camera.

Mancheno-Valencia A., Bologna-Molina R.E., Toussaint-Caire S., Vega-Memije M.E, & Cuevas-González J.C. (2018). Expression of E-cadherin, syndecan 1, Ki-67, and maintenance minichromosome 3 in tissue lesions of actinic prurigo obtained by incisional biopsy. Indian journal of pathology & microbiology, 61(2).

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