ADAM Metallopeptidase Domain 33 Proteine (ADAM33)

ADAM33 encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Zusätzlich bieten wir Ihnen ADAM33 Antikörper (67) und ADAM33 Kits (29) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
ADAM33 110751 Q923W9
ADAM33 80332 Q9BZ11
Ratte ADAM33 ADAM33 311425  
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Showing 4 out of 7 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Insektenzellen Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Anmelden zum Anzeigen 50 bis 55 Tage
Insektenzellen Maus rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Anmelden zum Anzeigen 50 bis 55 Tage
Wheat germ Human GST tag 10 μg Anmelden zum Anzeigen 11 bis 12 Tage
Escherichia coli (E. coli) Human S tag,His tag 100 μg Anmelden zum Anzeigen 15 bis 18 Tage

ADAM33 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Mouse (Murine)
Human , ,
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Weitere Proteine zu ADAM Metallopeptidase Domain 33 (ADAM33) Interaktionspartnern

Xenopus laevis ADAM Metallopeptidase Domain 33 (ADAM33) Interaktionspartner

  1. Here, the authors show that adam13 interacts with the arid3a/dril1/Bright transcription factor. This interaction promotes a proteolytic cleavage of arid3a and its translocation to the nucleus where it regulates another transcription factor: tfap2alpha. Tfap2alpha in turn activates multiple genes including the protocadherin pcdh8l (PCNS).

  2. Increased ADAM13 cleavage of cadherin 11produces the EC1-3 fragment which increases cranial neural crest cell invasiveness in vitro and blocks the repulsive contact inhibition of locomotion response in colliding cells.

  3. Novel roles for Plk and GSK3 regulation of ADAM13 function in cranial neural crest cell migration.

  4. Data show that ADAM13 function is autonomous to cranial neural crest (CNC) tissue.

  5. The cytoplasmic domain of ADAM13 regulates the expression of multiple genes in cranial neural crest, including the protease Calpain8-a.

Human ADAM Metallopeptidase Domain 33 (ADAM33) Interaktionspartner

  1. There was no significant difference in ADAM33 genotype and allele distributions between psoriasis and control groups (p > 0.05). CONCLUSIONS: ADAM33 V4 C/G rs2787094 polymorphism was not associated with psoriasis risk in the Turkish population.

  2. A lower level of ADAM33 was also correlated with shorter overall survival and metastasis-free survival and was considered an independent prognostic factor suggesting that ADAM33 is a novel molecular biomarker of Triple-negative breast cancer and basal-like phenotype that might be useful as a prognostic factor.

  3. IL4RA and ADAM33 variants may be risk markers of asthma exacerbations in type-2 inflammatory endotype. Precise endotyping may facilitate the identification of genetic risk markers of asthma exacerbations.

  4. Collectively, our findings suggest that 1,25(OH)2D3 inhibits VEGF-induced ASM cell proliferation by suppressing VEGFR2 and ERK1/2 activation and downregulating ADAM33. Further studies of these mechanisms are needed to facilitate the development of treatments for smooth muscle hyperplasia-associated diseases of the airway such as asthma.

  5. meta-analysis suggested that ADAM33 polymorphisms rs2280091, rs2280090, rs2787094, rs44707 and rs528557 were significantly associated with a high risk of childhood asthma

  6. There was a significant difference in the frequency of ADAM33 V4 polymorphism in both, asthmatic and COPD patients groups. No significant differences were found for T1 polymorphism. However, there were significant differences when haplotypes and diplotypes of ADAM33 V4/T1 were compared in all three groups. It can be concluded that the polymorphism V4 of ADAM33 is associated with asthma or COPD in Venezuelan patients.

  7. Evidence from this meta-analysis demonstrates that ADAM33 T1 polymorphism might be associated with increased susceptibility to asthma among Asian children and that ADAM33 F + 1, T2, S2, or V4 polymorphism may be unrelated to susceptibility of childhood asthma.

  8. enhances ADAM-33 expression and airway smooth muscle cell proliferation

  9. An association between ADAM33 gene polymorphism and impaired lung functions was detected in wood dust-exposed workers.

  10. This meta-analysis demonstrates that the ADAM33 gene polymorphisms confer susceptibility to allergic rhinitis

  11. findings suggest that genetic variants of ADAM33 gene may play important roles in asthma susceptibility in the Punjabi population of Pakistan

  12. We investigated the influence of ADAM33 polymorphisms on the serum levels of ADAM33 and the susceptibility to pediatric asthma in the Chinese Han population

  13. ADAM33 and ADAM12 genetic polymorphisms and their expression in Egyptian children with asthma

  14. the ADAM33 T1, T2, S1, Q-1, F+1 and ST+5 six locus polymorphisms association with the risk of COPD.

  15. a compromised ADAM33 gene may be implicated in the progression of wheeze into childhood asthma

  16. Our results suggest that the ADAM33 V4 polymorphism increases the risk of asthma.

  17. the intima+media of IPAH vessels, collagens (COL4A5, COL14A1, and COL18A1), matrix metalloproteinase (MMP) 19, and a disintegrin and metalloprotease (ADAM) 33 were higher expressed, whereas MMP10, ADAM17, TIMP1, and TIMP3 were less abundant.

  18. The results of this study suggest that these proteins play important roles in pulmonary inflammatory reactions elicited against etiological viral agents.

  19. Association between ADAM33 polymorphisms and susceptibility with adult and childhood asthma among Jordanians.

  20. ADAM33 was involved in the pathogenesis of chronic obstructive pulmonary disease in an East Asian population by affecting airway inflammation and immune response.

ADAM33 Protein Überblick

Protein Überblick

This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This protein is a type I transmembrane protein implicated in asthma and bronchial hyperresponsiveness. Alternative splicing of this gene results in two transcript variants encoding different isoforms.

Genbezeichner und Symbole assoziert mit ADAM33

  • ADAM metallopeptidase domain 33 (ADAM33)
  • disintegrin and metalloproteinase domain-containing protein 19-like (LOC100230755)
  • a disintegrin and metallopeptidase domain 33 (Adam33)
  • ADAM metallopeptidase domain 33 L homeolog (adam33.L)
  • ADAM metallopeptidase domain 33 (Adam33)
  • adam13 Protein
  • ADAM33 Protein
  • Adaml Protein
  • C20orf153 Protein
  • DJ964F7.1 Protein

Bezeichner auf Proteinebene für ADAM33

a disintegrin and metalloprotease 13 , disintegrin and metalloproteinase domain-containing protein 33 , ADAM metallopeptidase domain 33 , disintegrin and metalloproteinase domain-containing protein 33-like , ADAM 33 , a disintegrin and metalloprotease domain 33 , a disintegrin and metalloprotease domain 13 , x-adam 13 , a disintegrin and metalloprotease 33 , a disintegrin and metalloproteinase domain 33 , disintegrin and reprolysin metalloproteinase family protein , a disintegrin and metallopeptidase domain 33

422948 Gallus gallus
458061 Pan troglodytes
485795 Canis lupus familiaris
523627 Bos taurus
100066376 Equus caballus
100230755 Taeniopygia guttata
100356023 Oryctolagus cuniculus
100436114 Pongo abelii
110751 Mus musculus
386623 Xenopus laevis
80332 Homo sapiens
311425 Rattus norvegicus
Ausgewählte Anbieter für ADAM33 Proteine (ADAM33)
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