Nup62-il4i1 ELISA Kits

There are a number of ELISA Kits available for the measurement of Nup62-il4i1, another term for the human protein, interleukin 4 induced 1. Other synonyms may include: L-amino-acid oxidase, Fig-1 protein, IL4-induced protein 1, interleukin four induced 1, LAAO, and LAO. It is encoded by the IL4I1 gene to yield a protein 567 amino acids in length and 62.9 kDa in size. However, there are up to 2 reported isoforms. The protein is categorized into the Flavin monoamine oxidase family, FIG1 subfamily. Versions of Nup62-il4i1 are present in other organisms, including: Mouse, Rat, Frog, Chicken.

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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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Effective PBMC Staining with an Optimized Santa Cruz Antibody

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We were trying to validate GAPDH as an intracellular reference protein in PBMCs from healthy blood donors using flow cytometry. Had some initial trouble with the background, but sorted it out eventually. Overall, happy with the results.
Limited Performance Observed with Rabbit Polyclonal Unc93a Antibody

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We created a construct for the overexpression of UNC93A and transiently transfected it into HEK293T cells. The FLAG-tagged UNC93A protein was easily detected with an anti-FLAG antibody. However, we were unable to identify a corresponding band using the UNC93A antibody, even at a dilution of 1:100. These results indicate that while the overexpression construct is successfully expressed, the antibody does not recognize UNC93A under the conditions used for Western blotting.

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