Dp 70 color camera

Manufactured by Olympus

Sourced in Japan

The Olympus DP-70 is a high-performance color camera designed for use in various laboratory applications. It features a high-resolution CCD sensor and advanced imaging capabilities, providing accurate and detailed color reproduction. The DP-70 is capable of capturing high-quality digital images, making it a reliable tool for microscopy, documentation, and other scientific imaging tasks.

Automatically generated - may contain errors

Lab products found in correlation

Bx51 microscope, by Olympus (2 mentions) Bx51tf microscope, by Olympus (1 mentions) Ab64238, by Abcam (1 mentions) Picro sirius red stain kit, by Abcam (1 mentions) Hematoxylin mhs16, by Merck Group (1 mentions) 3050s cryostat, by Leica (1 mentions) Sab5500058, by Merck Group (1 mentions) Axio scan z1 slide scanner, by Zeiss (1 mentions)

5 protocols using dp 70 color camera

Retinal Cell Density Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols

The prepared 5 μm-thick tissue sections were brought to room temperature and deparaffinized. The tissue sections were then stained with hematoxylin (Bio Lab Diagnostics, Mumbai, India) for 15 minutes and counterstained with 1% eosin (Bio Lab Diagnostics) for another 15 minutes. After dehydration by treating with ethanol at 50% concentrations for 2 minutes, 65% for 2 minutes, 85% for 2 minutes, 90% for 2 minutes, 100% for 10 minutes, xylene: ethanol (1:1) for 6 minutes and xylene for 6 minutes, sections were observed at 400× magnification under a light microscope (Olympus BX51TF microscope with DP70 color camera, Olympus, Tokyo, Japan). The cell density of the retina was evaluated by counting the number of neuronal cells per 0.1 mm² area using the Cell Counter plugin of ImageJ v1.47 (Rasband, W.S., National Institutes of Health, Bethesda, MD, USA).

Faiq M.A., Sengupta T., Nath M., Velpandian T., Saluja D., Dada R., Dada T, & Chan K.C. (2022). Ocular manifestations of central insulin resistance. Neural Regeneration Research, 18(5), 1139-1146.

+ Open protocol

+ Expand

Histological Analysis of Mouse Liver Fibrosis

Check if the same lab product or an alternative is used in the 5 most similar protocols

4% paraformaldehyde-fixed livers were embedded in paraffin at the Johns Hopkins School of Medicine Pathology Core. Paraffin sections were cut, and hematoxylin and eosin stained at the Pathology Core. To analyze fibrosis, paraffin sections were stained using a Picro Sirius Red Stain Kit (ab150681, Abcam) according to the manufacturer’s instructions. To immunostain CK19, Ki67, and active caspase-3, paraffin sections were deparaffinized, subjected to antigen retrieval with 1 mM EDTA using a pressure cooker for 15 min, and incubated with the primary antibody at 4°C overnight. After washes with PBS, the samples were incubated with HRP-conjugated secondary antibody for 1 h at room temperature and stained with DAB (ab64238, Abcam). Hematoxylin (MHS16, Sigma-Aldrich) was used to counterstain nuclei. The samples were viewed using an Olympus BX51 microscope equipped with a DP-70 color camera.

Kato T., Murata D., Anders R.A., Sesaki H, & Iijima M. (2021). Nuclear PTEN and p53 suppress stress-induced liver cancer through distinct mechanisms. Biochemical and biophysical research communications, 549, 83-90.

+ Open protocol

+ Expand

Cryogenic Tissue Sectioning and Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols

After euthanasia, organs removed from CFZ and vehicle fed mice were cryo-preserved in optimal cutting temperature compound (Tissue-Tek 4583; Sakura). Tissue blocks were sectioned at a thickness 10 μm, using a Leica 3050S cryostat. For transmitted microscopy, cryo-sectioned slices were mounted on glass slides with glycerol, and imaged with Olympus X51 upright microscope equipped with X100 objective, DP-70 color camera, and DP controller 3.1.1267.

Keswani R.K., Baik J., Yeomans L., Hitzman C., Johnson A., Pawate A., Kenis P.J., Rodriguez-Hornedo N., Stringer K.A, & Rosania G.R. (2015). Chemical Analysis of Drug Biocrystals: A Role for Counterion Transport Pathways in Intracellular Drug Disposition. Molecular pharmaceutics, 12(7), 2528-2536.

+ Open protocol

+ Expand

Immunohistochemistry and Histology Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols

For immunohistochemistry, cryosections were stained with antibodies to B220 (1:100, Invitrogen; 14–0452-82) and CD3 (1:100, Sigma; SAB5500058). After washes with PBS, the samples were incubated with HRP-conjugated secondary antibody for 1 h at room temperature and stained with 3,3'-diaminobenzidine. For histology, paraformaldehyde-fixed tissues were embedded in paraffin at the Johns Hopkins School of Medicine Pathology Core. Paraffin sections were cut, and stained with hematoxylin and eosin. The samples were viewed using an Olympus BX51 microscope equipped with a DP-70 color camera.

Igarashi A., Kato T., Sesaki H, & Iijima M. (2021). Nuclear PTEN Deficiency and Heterozygous PTEN Loss Have Distinct Impacts on Brain and Lymph Node Size. Biochemical and biophysical research communications, 555, 81-88.

+ Open protocol

+ Expand

Epifluorescence Microscope Image Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols

Stained sections were imaged using BX51 epifluorescence microscope with DP70 color camera and CellSens software version 2.2 (Olympus, Tokyo, Japan) or the AxioScan.Z1 slide scanner with ZEN 2.6 software blue edition (Carl Zeiss, Oberkochen, Germany). Images were then quantified using FIJI ImageJ software version 1.52p (NIH, Bethesda, MD; https://imagej.nih.gov/ij). 15

Chan G., van Hummel A., van der Hoven J., Ittner L.M, & Ke Y.D. (2020). Neurodegeneration and Motor Deficits in the Absence of Astrogliosis upon Transgenic Mutant TDP-43 Expression in Mature Mice. The American journal of pathology, 190(8).

+ Open protocol

+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Revolutionizing how scientists
search and build protocols!