Age-Related Maculopathy Susceptibility 2 (ARMS2) Kits ELISA

ARMS2 encodes a protein that is thought to play a role in diseases in the elderly. De plus, nous expédions ARMS2 Anticorps (22) et ARMS2 Protéines (3) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
ARMS2 387715 P0C7Q2
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Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Humain 3.9 pg/mL 15.6-1000 pg/mL Typical standard curve 96 Tests Connectez-vous pour afficher 15 to 18 Days
$910.56
Détails

ARMS2 Kits ELISA mieux référencés

  1. Human ARMS2 Kit ELISA pour Sandwich ELISA - ABIN827448 : Ojalvo, Acosta, Marí, Mayola, Pérez, Gutiérrez, Marichal, Seijas, Kautzman, Pacheco, Armstrong: Healing enhancement of diabetic wounds by locally infiltrated epidermal growth factor is associated with systemic oxidative stress reduction. dans International wound journal 2017 (PubMed)

Plus Kits ELISA pour ARMS2 partenaires d'interaction

Human Age-Related Maculopathy Susceptibility 2 (ARMS2) interaction partners

  1. antioxidant and zinc nutritional supplement modifies risk of macular degeneration progression according to rs10490924 or 372_815del443ins54 genotype

  2. Our analysis showed stronger contribution of ARMS2 in age-related macular degeneration (AMD) with reticular pseudodrusen (RPD) group versus AMD without RPD group, in comparison with CFH genotypes.

  3. ARMS2 variants are likely associated with the 3-year outcomes of photodynamic therapy in patients with wet age-related macular degeneration.

  4. because the ARMS2/HTRA1 genes are positioned at a locus on chromosome 10q26 in a region with strong linkage disequilibrium, it is difficult to distinguish the functions of the individual genes. a review of recent epidemiological studies of Age-related macular degeneration(AMD) is offered. An argument for a definite correlation between the ARMS2 gene and AMD is presented

  5. In polypoidal choroidal vasculopathy patients, ARMS2 rs10490924 showed association with anatomic therapeutic response to anti-VEGF, suggesting pharmacogenetic relationship.

  6. The ARMS2 A69S polymorphism was associated with CNV recurrence rate in our patient cohort. Prediction of a greater risk of recurrence could help to design more appropriate follow-up treatment strategies for patients with neovascular AMD.

  7. Complement factor H Y402H (rs1061170) and age-related maculopathy susceptibility2 (ARMS2)/LOC387715 A69S (rs10490924) polymorphisms shown to have significant association with age-related macular degeneration (Meta-Analysis).

  8. The present meta-analysis revealed that the ARMS2 A69S risk variants confer a significantly greater risk of retinal angiomatous proliferation compared with neovascular age-related macular degeneration.

  9. we speculate that up-regulation of leptin and ARMS2 forms part of an important survival mechanism to compensate for placental growth discordance in monochorionic diamniotic twin pregnancies

  10. This analysis revealed the synergistic effect of these two factors indicating that there is a common pathway of ARMS2/LOC387715 and smoking in AMD pathogenesis which may be the complement system pathway.

  11. The findings of the present study provide evidence that CFH gene variants and ARMS2/HTRA1 genes play a major role in the genetic susceptibility to AMD in a Greek population. These findings are of direct relevance for disease and help mapping the genetic chart of AMD.

  12. Development of polypoidal choroidal vasculopathy (PCV) in the unaffected fellow eye is associated with ARMS2 A69S genotype in patients with unilateral PCV.

  13. OCT scans revealed lower retinal thickness in patients homozygous for CFH or ARMS2, which was caused by a significantly reduced photoreceptor layer. The number and ultrastructure of drusen were also significantly different.

  14. This study suggests that in familial age-related macular degeneration patients, the common genetic risk variant in ARMS2 is less important compared to sporadic age-related macular degeneration.

  15. this work we show that ARMS2 is externalized via an unconventional pathway bypassing Golgi.

  16. Interaction effects between supplement groups and individual complement factor H (CFH) Y402H and age-related maculopathy susceptibility 2 (ARMS2) genotypes, and composite genetic risk groups combining the number of risk alleles for both loci, were evaluated for their association with progression

  17. EMD were not AMD-independently associated with CFH or ARMS2 genotypes. Our results indicate that patients without AMD but with EMD can serve as controls in studies evaluating AMD risk factors.

  18. Variants in ARMS2 carry risk of age-related macular degeneration.

  19. CFH, ARMS2, and C3 were associated with specific features of neovascularization at the time patients were enrolled in Comparison of Age-Related Macular Degeneration Treatments Trials .

  20. Subfoveal choroidal thickness and choroidal vascular hyperpermeability in eyes with treatment-naive polypoidal choroidal vasculopathy were associated with ARMS2 A69S (rs10490924) and CFH (rs1329428).

ARMS2 profil antigène

Antigen Summary

This gene encodes a protein that is thought to play a role in diseases in the elderly. Mutations in this gene have been associated with age-related macular degeneration.

Gene names and symbols associated with ARMS2

  • age-related maculopathy susceptibility 2 (ARMS2) anticorps
  • ARMD8 anticorps
  • ARMS2 anticorps

Protein level used designations for ARMS2

age-related maculopathy susceptibility protein 2 , age-related maculopathy susceptibility 2

GENE ID SPECIES
387715 Homo sapiens
450791 Pan troglodytes
100271852 Macaca mulatta
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