Mouse Serine/threonine/tyrosine-interacting protein (STYX) ELISA Kit

MTMR8 encodes a myotubularin-related protein that, unlike most other members of the myotubularin-related protein family, has no dual-specificity phosphatase domain. Myotubularin-related protein 9 is a myotubularin-related protein that is atypical to most other members of the myotubularin-related protein family because it has no dual-specificity phosphatase domain. The encoded protein contains a double-helical motif similar to the SET interaction domain, which is thought to have a role in the control of cell proliferation. In mouse, a protein similar to the encoded protein binds with MTMR7, and together they dephosphorylate phosphatidylinositol 3-phosphate and inositol 1,3-bisphosphate.

The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Mouse Serine/threonine/tyrosine-interacting protein (STYX) ELISA Kit has high sensitivity and excellent specificity for detection of Mouse STYX. No significant cross-reactivity or interference between Mouse STYX and analogues was observed.

This Mouse Serine/threonine/tyrosine-interacting protein (STYX) ELISA Kit employs a two-site sandwich ELISA to quantitate STYX in samples. An antibody specific for STYX has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySTYX present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for STYX is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of STYX bound in the initial step. The color development is stopped and the intensity of the color is measured.

• Do not mix components from different kit lots or use reagents beyond the kit expiration date.• Allow all reagents to warm to room temperature for at least 30 minutes before opening.• Pre-rinse the pipet tip with reagent, use fresh pipet tips for each sample, standard and reagent to avoid contamination.• Unused wells must be kept desiccated at 4 °C in the sealed bag provided.• Mix Thoroughly is very important for the result. It is recommended using low frequency oscillator or slight hand shaking every 10 minutes.• It is recommended that all samples and standards be assayed in duplicate or triplicate.