The largest database of trusted experimental protocols

Hamamatsu digital camera c11440

Manufactured by Hamamatsu Photonics
Sourced in United States

The HAMAMATSU digital camera C11440 is a high-performance camera designed for scientific and industrial applications. It features a large-format sensor with a resolution of 4096 x 4096 pixels, enabling the capture of detailed, high-quality images. The camera offers a wide dynamic range and low noise characteristics, making it suitable for a variety of imaging tasks. Its compact and robust design allows for easy integration into various systems and setups.

Automatically generated - may contain errors

2 protocols using hamamatsu digital camera c11440

1

Immunofluorescence Staining of Kidney Sections

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunofluorescence staining was performed on O.C.T-embedded frozen kidneys, which were sectioned at 8 µm before staining. Kidney sections were fixed in 4% PFA (Fisher Scientific, Waltham, MA, USA) before staining. Primary antibodies of thrombin, CD31, VCAM-1, NLRP3, Caspase-11, IL-1beta, or IL-18 (Abcam, Waltham, Boston, MA, USA) were applied onto the frozen section for 1 h at room temperature, followed by the corresponding secondary antibodies against rabbit labeled with Alex 594 or Cy5.5 (Abcam, Waltham, Boston, USA) incubation at room temperature for 30 min. Slides were then mounted with VECTASHIELD antifade mounting medium with DAPI (Vector Laboratories, Newark, CA, USA) before being imaged with an Olympus dark-field microscope outfitted with a HAMAMATSU digital camera C11440 at 20× or 40× magnification. Double-blind data acquisition was performed on all images.
+ Open protocol
+ Expand
2

Histological and Immunofluorescence Analysis of Kidney Tissue

Check if the same lab product or an alternative is used in the 5 most similar protocols
10% formalin-fixed kidneys were further processed, sectioned, and H&E stained at the Anatomic and Molecular Pathology Core Histology Lab of the Department of Pathology and Immunology, Washington University School of Medicine. Microscopic images of the H&E slides were acquired with an Olympus bright-field microscope outfitted with a DP27 digital camera to record images of the tissue sections at 20× magnification.
Immunofluorescence staining was performed on O.C.T-embedded frozen kidneys, which were sectioned at 8 µm before staining. Kidney sections were fixed in 4% PFA (Thermo Scientific, Waltham, MA, USA) before staining. Primary rabbit antibodies to p62, ICAM-1, VCAMM-1, and Bax (Abcam, Waltham, MA, USA) were applied onto the frozen section for 1 h at room temperature, followed by the secondary anti-rabbit antibody labeled with Alex 594 (Abcam, Waltham, MA, USA), and the tissue section was incubated at room temperature for 30 min. Slides were then mounted using VECTASHIELD antifade mounting medium with DAPI (Vector Laboratories, Newark, CA, USA), before imaging with an Olympus dark-field microscope outfitted with a HAMAMATSU digital camera C11440 at 40× magnification. Double-blind data acquisition was performed on all images. Blinded data analysis was performed on all kidney images by an experienced renal pathologist (J.G.).
+ 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?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!