platelet-activating factor acetylhydrolase 2, 40kDa ELISA Kits

Listed are ELISA Kits for the detection of platelet-activating factor acetylhydrolase 2, 40kDa, an alias name of platelet activating factor acetylhydrolase 2. The human protein, encoded by the gene PAFAH2, is 392 amino acid residues long and has a mass of 44,036 daltons. It is an enzyme of the 1-alkyl-2-acetylglycerophosphocholine esterase class and is a member of the Serine esterase family. This protein is reported to have a cytoplasmic cellular localization. For this target protein, ELISA kits with the following species reactivities are available: human, mouse, rat, and bovine. This target may also be known as: platelet-activating factor acetylhydrolase 2 cytoplasmic, SD-PLA2, platelet-activating factor acetylhydrolase 2 40kDa, and serine-dependent phospholipase A2.

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Human Albumin ELISA Kit
The Bethyl Human Albumin ELISA Kit enables quantitative detection of albumin in serum, plasma, CSF, milk, and urine. Using a sandwich ELISA format, it provides sensitive, colorimetric measurement via antibody binding and enzymatic reaction. Ideal for up to 40 duplicate samples, it supports clinical research and monitoring of conditions affecting albumin levels. The kit is ready for immediate use with all required components included for streamlined and reliable testing.
ChemiDoc™ MP Imaging System
Set up a live demo with a Bio-Rad Imaging Specialist - Request a DemoUse the ChemiDoc MP Imaging System for flexible, high-sensitivity multiplex fluorescent and chemiluminescence western blot detection, imaging gels, analysis and documentation. This system is compatible with a wide range of fluorophores (see the fluorophore compatibility chart), such as StarBright™ Secondary Antibodies, ethidium bromide, SYPRO Ruby, Coomassie, and silver stains.Features and Benefits Sensitive detection &#...

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Ly-6G Monoclonal Antibody from Thermo Fisher Shows Excellent Performance with Recommended Staining Protocol

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This antibody worked very well and provided clear, distinct staining with minimal background. The signal was strong and reproducible, making it reliable for flow cytometry analysis.
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