ImmunoChemistry Technologies

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HRP Goat Anti-Rabbit IgG Fc
HRP Goat Anti-Mouse IgG Fc
HRP Goat Anti-Human IgG Fc
Pack of Desiccant Packets
Native Human Cathepsin D
Figure 1. Fluorescence spectraFigure 2. Jurkat cells were exposed to 3% formaldehyde for 30 minutes. Following the formaldhehyde treatment, cells were stained with Green Live/ Dead stain and then imaged with a Nikon E800 microscope (DIC overlay shown). Cells with compromised membranes stained green, while cells with intact membranes excluded the Green Live/Dead stain and remained unstained. Data courtesy of Mrs. Tracy Murphy, ICT.
DAPI Nuclear StainImmunolabeling of an organ cultured human hair follicle treated with 1.25ug/ml of ICP5249 for 5 days labeling light chain 3 I/II (green) and DAPI (Cat. 6244, blue) was used for nuclear staining. Image from publication. CC-BY-4.0 PMID: 39155393
Fixative
Figure 1. A pool of Jurkat cells was spiked with FAM-YVAD-FMK (Cat. 9146) and divided into separate treatment groups. Starting with 24 hour samples and working backwards, 10 µM Nigericin was added to cells and the samples were incubated at 37°C throughout the induction process. The cells were washed and analyzed on a flow cytometer. The level of caspase-1 activity directly correlated to the period of exposure to Nigericin Data. courtesy of Mrs. Tracy Murphy, ICT (220:78).

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