ATPase, H transporting, lysosomal V1 subunit F ATPase, H+ transporting, lysosomal V1 subunit F ELISA Kits

Listed are ELISA Kits for the detection of ATPase, H+ transporting, lysosomal V1 subunit F, an alias name of ATPase H+ transporting V1 subunit F. The human protein, encoded by the gene ATP6V1F, is 119 amino acid residues long and has a mass of 13,370 daltons. However, there are up to 2 reported isoforms. It is a member of the V-ATPase F subunit family. This target may also be known as: V-type proton ATPase subunit F, ATPase H+ transporting lysosomal 14kDa V1 subunit F, ATPase vacuolar 14 kD, H(+)-transporting two-sector ATPase 14kD subunit, V-ATPase F subunit, V-ATPase subunit F, and adenosinetriphosphatase 14k chain.

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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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