A Disintegrin and Metalloproteinase with Thrombospondin Motifs 17 (ADAMTS17), E

For Research Use Only. Not for use in diagnostic procedures.

Store at 2 to 8 degree C for 6 months.

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Small volumes of ADAMTS17 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS166834 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the A Disintegrin and Metalloproteinase with Thrombospondin Motifs 17 (ADAMTS17) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing ADAMTS17. The ELISA analytical biochemical technique of the MBS166834 kit is based on ADAMTS17 antibody-ADAMTS17 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect ADAMTS17 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, ADAMTS17. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).

54,757 Da

ADAM metallopeptidase with thrombospondin type 1 motif 17

A disintegrin and metalloproteinase with thrombospondin motifs 17

A disintegrin and metalloproteinase with thrombospondin motifs 17

ADAM-TS 17; ADAM-TS17; ADAMTS-17  [Similar Products]

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016]

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