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ADAMTS9 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Zusätzlich bieten wir Ihnen ADAMTS9 Antikörper (22) und und viele weitere Produktgruppen zu diesem Protein an.
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Human ADAMTS9 ELISA Kit für Sandwich ELISA - ABIN1118181
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 2017
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.
a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 9
, A disintegrin and metalloproteinase with thrombospondin motifs 9
, ADAM-TS 9