Mouse Tenomodulin (TNMD) ELISA Kit

By searching an EST database for sequences similar to mouse Tem, followed by RACE of a human fetus cDNA library, Shukunami et al. (2001) cloned TEM. The deduced 317-amino acid protein contains an N-terminal transmembrane domain and a putative antiangiogenic domain with 8 cysteines. TEM shares 96% amino acid identity with mouse Tem, and it shares 65% identity in a 65-amino acid C-terminal stretch with chondromodulin I (CHM1) . Northern blot analysis of several mouse tissues detected a 1.4-kb transcript expressed specifically in skeletal muscle. In situ hybridization revealed mouse Tem expression in dense connective tissue, such as epimysium and tendon.

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Mouse Tenomodulin (TNMD) ELISA Kit has high sensitivity and excellent specificity for detection of Mouse TNMD. No significant cross-reactivity or interference between Mouse TNMD and analogues was observed.

This Mouse Tenomodulin (TNMD) ELISA Kit employs a two-site sandwich ELISA to quantitate TNMD in samples. An antibody specific for TNMD has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTNMD present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for TNMD 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 TNMD 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.