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ADAMTS17 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Zusätzlich bieten wir Ihnen ADAM Metallopeptidase with thrombospondin Type 1 Motif, 17 Kits (13) und und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal ADAMTS17 Primary Antibody für WB - ABIN6243834
Hubmacher, Schneider, Berardinelli, Takeuchi, Willard, Reinhardt, Haltiwanger, Apte: Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease. in Scientific reports 2017
higher Adamts17 expression is found in several human cancer cell subtypes, especially in breast ductal carcinoma and there is an inverse correlation between higher Adamts17 expression and patients' survival.
A mutation in WMS (zeige FBN1 Antikörper)-like gene ADAMTS17 also causes WMS (zeige FBN1 Antikörper).
Endothelial protease nexin-1 (zeige SERPINE2 Antikörper) is a novel regulator of A disintegrin and metalloproteinase 17 (zeige ADAM17 Antikörper) maturation and endothelial protein C receptor (zeige PROCR Antikörper) shedding via furin (zeige FURIN Antikörper) inhibition.
Recessive ADAMTS17 mutations are a recurrent cause of isolated spherophakia with short stature.
ADAMTS17 is a target gene of the BACH1 (zeige BACH1 Antikörper) transcription factor according to ChIP-seq analysis in HEK (zeige EPHA3 Antikörper) 293 cells.
Homozygous mutation in ADAMTS17 causes lenticular myopia, ectopia lentis, glaucoma, spheropakia, and short stature.
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 protein encoded by this gene has a high sequence similarity to the protein encoded by ADAMTS19, another family member. The function of this protein has not been determined.
ADAM metallopeptidase with thrombospondin type 1 motif, 17
, disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 17
, A disintegrin and metalloproteinase with thrombospondin motifs 17
, ADAM-TS 17
, a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 17
, A disintegrin and metalloproteinase with thrombospondin motifs 17-like