(ADAM Metallopeptidase with thrombospondin Type 1 Motif, 9 (ADAMTS9))
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family 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. Members of the ADAMTS family have been implicated in the cleavage of proteoglycans, the control of organ shape during development, and the inhibition of angiogenesis. This gene is localized to chromosome 3p14.3-p14.2, an area known to be lost in hereditary renal tumors. [provided by RefSeq, Jul 2008].
Tajima, Sekimoto, Yamaguchi, Taniguchi, Kurogi, Maruyama, Chosa: "Hemoglobin stimulates the expression of ADAMTS-5 and ADAMTS-9 by synovial cells: a possible cause of articular cartilage damage after intra-articular hemorrhage." in: BMC musculoskeletal disorders, Vol. 18, Issue 1, pp. 449, (2018) (PubMed).
Aliases for ADAMTS9 ELISA试剂盒
ADAM metallopeptidase with thrombospondin type 1 motif 9 (ADAMTS9) ELISA试剂盒 a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 9 (Adamts9) ELISA试剂盒 ADAM metallopeptidase with thrombospondin type 1 motif, 9 (Adamts9) ELISA试剂盒 1810011L16Rik ELISA试剂盒 8430403M15Rik ELISA试剂盒 AW743315 ELISA试剂盒 E030027K14Rik ELISA试剂盒