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ADAMTS4 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, 4 Antikörper (152) und ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 4 Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
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Human ADAMTS4 ELISA Kit für Sandwich ELISA - ABIN649162
Zha, Chen, Xu, Zhang, Li, Zhao, Cui: Elevated level of ADAMTS4 in plasma and peripheral monocytes from patients with acute coronary syndrome. in Clinical research in cardiology : official journal of the German Cardiac Society 2010
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Moncada-Pazos, Obaya, Viloria, López-Otín, Cal: The nutraceutical flavonoid luteolin inhibits ADAMTS-4 and ADAMTS-5 aggrecanase activities. in Journal of molecular medicine (Berlin, Germany) 2011
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Human ADAMTS4 ELISA Kit für Sandwich ELISA - ABIN366270
Mao, Wu, Zhang, Zhang, Liao, Li, Kang: MicroRNA-92a-3p Regulates Aggrecanase-1 and Aggrecanase-2 Expression in Chondrogenesis and IL-1β-Induced Catabolism in Human Articular Chondrocytes. in Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2018
Human ADAMTS4 ELISA Kit - ABIN454126
Zha, Chen, Xu, Li, Zhao, Cui: ADAMTS4 level in patients with stable coronary artery disease and acute coronary syndromes. in Biomedicine & pharmacotherapy 2010
host-derived ADAMTS4 was expressed at the tumor vessels and was associated with early-stage tumor growth.
This study demonstrated that ADAMTS-4 is a new marker of mature oligodendrocytes contributing to the myelination processes and thus to the control of motor capacities.
results demonstrate for the first time that ADAMTS4 contributes to diet induced atherosclerosis in ApoE (zeige APOE ELISA Kits)(-/-) mice
the reduction of ADAMTS-4 activity during the progression of ALS pathology may be an adaptive change to mitigate its neurodegenerative impact in CNS tissues
Results show that ADAMTS15 (zeige ADAMTS15 ELISA Kits) and ADAMTS4 not only exhibit unique cellular expression patterns in the brain but their developmental upregulation by these cell types coincides with critical aspects of neural development
aggrecan (zeige ACAN ELISA Kits) and brevican (zeige BCAN ELISA Kits) proteolysis is compensated in Adamts4-/- or Adamts5 (zeige ADAMTS5 ELISA Kits)-/- mice by ADAMTS (zeige ADAMTS1 ELISA Kits) proteoglycanase (zeige MMP3 ELISA Kits) family members but a threshold of versican (zeige Vcan ELISA Kits) proteolysis is sensitive to the loss of a single ADAMTS (zeige ADAMTS1 ELISA Kits) proteoglycanase (zeige MMP3 ELISA Kits) during spinal cord injury
ADAMTS4 has roles in melanoma growth and angiogenesis in mice
The serine protease (zeige F2 ELISA Kits) tissue plasminogen activator (tPA (zeige PLAT ELISA Kits)) and two matrix metalloproteinases, ADAMTS-4 and ADAMTS-5 (zeige ADAMTS5 ELISA Kits), were identified as Reelin (zeige RELN ELISA Kits) cleaving enzymes.
ADAMTS-4 cleaves Reelin (zeige RELN ELISA Kits) in an isoform-specific manner. Among ADAMTS-4 isoforms, p50 (zeige LSP1 ELISA Kits) cleaves the N-t site only, while p75 (zeige NGFR ELISA Kits) cleaves both sites.
Data demonstrate that Adamts1 (zeige ADAMTS1 ELISA Kits) and Adamts4 play redundant and essential roles in perinatal kidney development.
ADAMTS 1 (zeige ADAMTS1 ELISA Kits), 4, 12, and 13 levels in the maternal and cord blood were lower in the preeclampsia group than in the control group. ADAMTS 1 (zeige ADAMTS1 ELISA Kits), 4, and 12 levels in placental tissues were higher in the preeclampsia group.
ADAMTS4 was associated macrophages infiltration and polarization in the tumor microenvironment of CRC (zeige CALR ELISA Kits) and ADAMTS4 knockdown had no inhibitory implications on cell proliferation and invasion in vitro, but significantly attenuated tumor growth in vivo.
ADAMTS4 expression was upregulated during carotid atherosclerotic plaque development. Serum levels of ADAMTS4 were associated with increased plaque vulnerability in both symptomatic and asymptomatic patients with carotid artery stenosis.
methylation status of the ADAMTS4 gene is altered in patellar tendinopathy
HipHop-based pharmacophore modeling and virtual screening of the Maybridge database to identify novel ADAMTS-4 inhibitors. These novel lead compounds act as potent and specific inhibitors for the ADAMTS-4 enzyme and could have therapeutic potential in the treatment of OA.
ADAMTS-4 protein expression increased in cartilage tissue from spinal tuberculosis patients.
Using in vitro approaches and cultured breast cancer cell lines authors demonstrate that Fibulin-2 (zeige FBLN2 ELISA Kits) is a better substrate for ADAMTS-5 (zeige ADAMTS5 ELISA Kits) than it is for ADAMTS-4. Fibulin-2 (zeige FBLN2 ELISA Kits) degradation is associated to an enhancement of the invasive potential of T47D, MCF-7 and SK-BR-3 cells.
ADAMTS4 and ADAMTS15 (zeige ADAMTS15 ELISA Kits) were upregulated in symptomatic uterine leiomyomas.
The SNP rs4233367 in the exon of ADAMTS-4 gene may be associated with lumbar disc degeneration.
Single Nucleotide Variants of Candidate Genes in Aggrecan (zeige ACAN ELISA Kits) Metabolic Pathway Are Associated with Lumbar Disc Degeneration and Modic Changes
ADAMTS4 participates in the regulation of muscle development in cattle.
aggrecanase activity (a) is responsible for early TNFalpha (zeige TNF ELISA Kits)-dependent aggrecan (zeige ACAN ELISA Kits) cleavage and GAG release in the meniscus and (b) might be involved in meniscal degeneration.
ADAMTS4 and ADAMTS5 (zeige ADAMTS5 ELISA Kits) are inhibited by alpha2-macroglobulin (zeige A2M ELISA Kits)
identified multiple conserved amino acids within regions N- and C-terminal to the site of scission that may influence enzyme-substrate recognition, and may interact with exosites on ADAMTS-4 and ADAMTS-5 (zeige ADAMTS5 ELISA Kits)
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. The enzyme encoded by this gene lacks a C-terminal TS motif. It is responsible for the degradation of aggrecan, a major proteoglycan of cartilage, and brevican, a brain-specific extracellular matrix protein. The cleavage of aggrecan and brevican suggests key roles of this enzyme in arthritic disease and in the central nervous system, potentially, in the progression of glioma.
A disintegrin and metalloproteinase with thrombospondin motifs 4
, ADAM-TS 4
, a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 4
, a disintegrin and metallopeptidase with thrombospondin motifs 4
, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 4
, ADAM metallopeptidase with thrombospondin type 1 motif, 4
, A disintegrin and metalloproteinase with thrombospondin motifs 4-like
, disintegrin and metalloproteinase with thrombospondin motifs 2
, a disintegrin and metalloproteinase with thrombospondin motifs 4