The largest database of trusted experimental protocols

Digital sight ds l1 camera

Manufactured by Nikon

The Digital Sight DS-L1 camera is a compact, high-resolution digital camera designed for laboratory and scientific applications. It features a CMOS sensor with a resolution of up to 5.0 megapixels and supports a variety of image capture modes, including live view, time-lapse, and high-speed recording. The camera is compatible with Nikon F-mount lenses and can be controlled via a computer interface or the camera's on-board controls.

Automatically generated - may contain errors

6 protocols using digital sight ds l1 camera

1

RNAi Screening in Caenorhabditis elegans

Check if the same lab product or an alternative is used in the 5 most similar protocols
The RNAi clones used here were obtained from the RNAi feeding library constructed by Julie Ahringer’s group at The Wellcome CRC Institute (University of Cambridge, Cambridge, UK) and distributed by Source BioScience, with the exception of mttu-1(RNAi) which was constructed in this work (see S1 Text). Plasmids were transformed into HT115 E. coli competent cells as indicated. let-92(RNAi) and the empty plasmid L4440 were transformed into HT115 E. coli cells to be used as a positive and negative controls, respectively. For the RNAi treatment, worms were synchronized by hypochlorous acid treatment and L4 animals were transferred to the NGM plates with HT115 bacteria expressing the dsRNA. Lifespan assays were performed directly on those L4 worms, while for the remaining RNAi assays the phenotypes of the progeny of the silenced L4 worms were assessed (unless otherwise specified). In order to analyze the number of progeny, the silenced one-day adult worms were transferred to a new plate containing bacteria expressing the dsRNA. When nematodes had finished laying eggs, they were removed from the plate. Worms were imaged on plates with a Nikon Digital Sight DS-L1 camera.
+ Open protocol
+ Expand
2

HRMVEC Migration Measured by Wound-Healing

Check if the same lab product or an alternative is used in the 5 most similar protocols
HRMVEC migration was measured by wound-healing assay. Briefly, endothelial cells were plated in ibidi culture insert at 2 × 104 cells/chamber, grown to full confluence and growth-attested in medium 131 without any growth supplements for 24 hrs. After the growth-arresting period, the ibidi inserts were removed and 1 ml of medium 131 containing 5 mM hydroxyurea was added. Cells were treated with and without VEGFA (40 ng/ml) for 24 hrs and the migrated cells were observed under Nikon Eclipse TS100 microscope with 4X/0.13 magnification and the images were captured with a Nikon Digital Sight DS-L1 camera. The cell migration was calculated using ImageJ and expressed as percent wound closure (total area at 0 hrs-area not occupied by the cells at 24 hrs/total area at 0 hrs X 100).
+ Open protocol
+ Expand
3

Quantitative Analysis of CA1 Region

Check if the same lab product or an alternative is used in the 5 most similar protocols
The tissue IR was analyzed at 10× (air objective, NA 0,25, Nikon) magnification by light microscopy (Nikon Epsilon E200) with a Nikon digital sight DS-L1 camera. For each slide, two consecutive images were taken allowing encompass all the extension of CA1 area for its analysis. The images were transformed to 8-bit and then analyzed using the binary threshold in the ImageJ software (NIH ImageJ). To calculate the total stained area, segmentation of all images was performed using intensity thresholding.
+ Open protocol
+ Expand
4

Immunohistochemical Staining of Macrophages

Check if the same lab product or an alternative is used in the 5 most similar protocols
Aortic root sections were fixed in an equal volume of cold acetone and methanol for 10 min, permeabilized in 0.2% Triton X-100 for 10 min and blocked with 3% BSA for 30 min. The sections were then incubated with anti-Mac3 primary Ab (1:200) overnight at 4 °C, which was followed by incubation with biotin-conjugated goat anti-rat secondary Ab (1:500) for 1 h at room temperature. The sections were incubated with the ABC (avidin–biotin complex) reagent for 30 min, developed with DAB (3,3'-diaminobenzidine) reagent (Vector Laboratories) and counterstained with haematoxylin. The sections were observed under a Nikon Eclipse 50i microscope with × 4/0.10 or × 10/0.25 magnification and the images were captured with a Nikon Digital Sight DS-L1 camera.
+ Open protocol
+ Expand
5

Macrophage and SMC Migration Assays

Check if the same lab product or an alternative is used in the 5 most similar protocols
Macrophage migration was measured using a modified Boyden chamber method.54 (link) Macrophages from WD-fed ApoE−/− and ApoE−/−:Pak1−/− mice were suspended in DMEM medium and plated on matrigel-coated 8 μm cell culture inserts at 5 × 104 cells per insert. MCP-1 was added to a final concentration of 50 ng/ml to the lower chamber, and the cells were incubated for 8 hours at 37°C. The inserts were then lifted, nonmigrated cells on the upper surface of the membrane were removed with a cotton swab, and the membrane was then fixed in methanol and stained with 4′,6-diamidino-2-phenylindole (DAPI). The DAPI-positive cells on the lower surface of the membrane were counted under an inverted microscope (Carl Zeiss AxioVision AX10), and the cell migration was expressed as the number of cells per field of view. SMC migration was measured by wound-healing assay. Briefly, SMCs were plated at 2 × 105 cells/ml in each chamber of the ibidi culture inserts, grown to full confluency and growth-arrested. Following a 24-hrs growth-arresting period, the inserts were removed using sterile tweezers and 2 ml of DMEM containing 5 mM hydroxyurea was added to the culture dish and incubation continued for 48 hrs. The migrated cells were observed under Nikon Eclipse TS100 microscope with 10X/0.25 magnification and the images were captured with a Nikon Digital Sight DS-L1 camera.
+ Open protocol
+ Expand
6

Macrophage and Smooth Muscle Cell Migration Assays

Check if the same lab product or an alternative is used in the 5 most similar protocols
Macrophage migration was measured using a modified Boyden chamber method54 (link). Macrophages from WD-fed ApoE−/− and ApoE−/−:Pak1−/− mice were suspended in DMEM medium and plated on Matrigel-coated 8-μm cell culture inserts at 5 × 104 cells per insert. MCP-1 was added to a final concentration of 50 ng ml−1 to the lower chamber and the cells were incubated for 8 h at 37 °C. The inserts were then lifted, non-migrated cells on the upper surface of the membrane were removed with a cotton swab and the membrane was then fixed in methanol and stained with DAPI (4′,6-diamidino-2-phenylindole). The DAPI-positive cells on the lower surface of the membrane were counted under an inverted microscope (Carl Zeiss AxioVision AX10) and the cell migration was expressed as the number of cells per field of view. SMC migration was measured by wound-healing assay. Briefly, SMCs were plated at 2 × 105 cells per ml in each chamber of the ibidi culture inserts, grown to full confluency and growth arrested. Following a 24-h growth-arresting period, the inserts were removed using sterile tweezers and 2 ml of DMEM containing 5 mM hydroxyurea was added to the culture dish, and incubation continued for 48 h. The migrated cells were observed under Nikon Eclipse TS100 microscope with × 10/0.25 magnification and the images were captured with a Nikon Digital Sight DS-L1 camera.
+ 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!