ATP Binding Cassette Transporter A3 (ABCA3) Kits ELISA

The membrane-associated protein encoded by ABCA3 is a member of the superfamily of ATP-binding cassette (ABC) transporters. De plus, nous expédions ABCA3 Anticorps (24) et et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
ABCA3 21 Q99758
Anti-Souris ABCA3 ABCA3 27410 Q8R420
Anti-Rat ABCA3 ABCA3 302973  
Comment commander chez anticorps-enligne
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Commandez enligne
  • orders@anticorps-enligne.fr

Top ABCA3 Kits ELISA sur anticorps-enligne.fr

Showing 1 out of 5 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Livraison Prix Détails
Humain 33 pg/mL 78.12 pg/mL - 5000 pg/mL 96 Tests 13 to 16 Days
$736.84
Détails

Plus Kits ELISA pour ABCA3 partenaires d'interaction

Human ATP Binding Cassette Transporter A3 (ABCA3) interaction partners

  1. we classified cellular consequences of missense ABCA3 sequence variations leading to pulmonary disease of variable severity. The corresponding molecular pathomechanisms of such ABCA3 variants may specifically be addressed by targeted treatments.

  2. Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age 34-36 weeks).

  3. Mutations in SFTPC, NKX2.1, and FOXF1 were identified among Japanese infants and children with childhood interstitial lung disease, whereas ABCA3 mutations were rare.

  4. The aim of this study was to prove that disease causing misfolding ABCA3 mutations can be corrected in vitro and to investigate available options for correction.

  5. Our results showed that the allele frequency of p.G1205R, but not p.L39V, was significantly higher in ILD patients than in healthy controls. However, no additional subject carrying the variant p.S828F or p.V968M was detected in the cohort analysis. These results indicate that the heterozygous ABCA3 gene variants may contribute to susceptibility to diseases in the Chinese population.

  6. a mutation (E292V) located in the first cytoplasmic loop of ABCA3 did not significantly affect lipid transport, but rather resulted in smaller vesicles. In addition to these findings, the assay used in this work for analysing the PC-lipid transport into ABCA3 positive vesicles will be useful to screen for compounds susceptible to restore function in mutated ABCA3 protein.

  7. Understanding the relationship between cholesterol and inflammation in the lung, and the role that ABC transporters play in this may illuminate new pathways to target for the treatment of inflammatory lung diseases

  8. two ABCA3 mutations (p.R288K and p.R1474W) identified among term and late-preterm infants with respiratory distress syndrome, were characterized.

  9. 1153 patients with diffuse parenchymal lung disease (DPLD) were registered in the KLR. The DNA of 242 of these patients was sequenced for ABCA3 mutations. 69 patients had at least one variation in the ABCA3 gene. Of 40 patients with two disease-causing ABCA3 mutations, 22 patients were homozygous and 18 heterozygous.

  10. Genes ABCC7, A3, A8, A12, and C8 prevailed among the most upregulated or downregulated ones. In conclusion, the results supported our theory about general adenosine triphosphate-binding cassette gene expression profiles and their importance for cancer on clinical as well as research levels.

  11. transporter oligomerization is crucial for ABCA3 function.

  12. The TGGAG haplotype may be a risk factor for Respiratory Distress Syndrome in preterm infants in this Chinese population. The haplotype TGGAG was significantly more frequent in RDS infants than in non-RDS infants.

  13. Rare mutations in surfactant-associated genes contribute to neonatal respiratory distress syndrome. We resequenced all exons of the ATP-binding cassette member A3 (ABCA3) and we found three ABCA3 mutations in the Han [minor allele frequency (MAF)=0.003] and 7 in the Zhuang (MAF=0.011) cohorts. The contribution of these rare ABCA3 mutations to disease burden in the south China population is still unknown.

  14. The clinical features of ABCA3 mutations, including onset, severity or clinical course are very heterogeneous. In the two siblings we had a lightly discordant course that could be explained by exposure to different environmental stresses or variable penetrance.

  15. These results provide evidence of ABCA3 as an MLF efflux transporter in human macrophages and support its role in the direct antileishmanial effect of this alkylphosphocholine drug.

  16. Studies indicate that ATP-binding cassette (ABC), subfamily A, member 3 (ABCA3) is developmentally regulated.

  17. Data discussed the structural features of ABCA3 and how the use of bioinformatics tools could help researchers to obtain a reliable structural model to locate relevant mutations and make genotype/phenotype correlations of affected patients. [review]

  18. SLCO1B3 699GG and 344TT genotypes are associated with non-response to IM, while ABCA3 4548-91 CC/CA genotypes are related to poor CMR in CML patients treated with standard-dose imatinib.

  19. Accumulation of free cholesterol as a result of a loss of ABCA3 export function represents a novel pathomechanism in ABCA3-induced Diffuse parenchymal lung disease.

  20. Report of ABCA3 mutations in a family with one child exhibiting interstitial lung disease.

Mouse (Murine) ATP Binding Cassette Transporter A3 (ABCA3) interaction partners

  1. mAbca3-rNeo mice demonstrated allele-dependent susceptibility to bleomycin including enhanced weight loss, augmented airspace destruction, and increased fibrosis

  2. Abca3 haploinsufficiency results in an altered biochemical and lung mechanical phenotype, as well as a greater lung injury induced by hyperoxia or mechanical ventilation.

  3. The majority of mice in which Abca3 was deleted in alveolar type II cells died shortly after birth from respiratory distress related to surfactant deficiency.

  4. Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter protein ABCA3

  5. showed for the first time expression and subcellular localization of abcb11 and abca3 in mouse kidney

  6. Plays an essential role in pulmonary surfactant lipid metabolism and lamellar body biogenesis, probably by transporting these lipids as substrates.

  7. ABCA3 is necessary for lamellar body biogenesis, surfactant protein-B processing, and lung development late in gestation.

  8. The phenotype of respiratory failure immediately after birth corresponds to the clinical course of severe ABCA3 mutations in human newborns.

  9. Abca3 gene expression is mediated by discrete cis-acting cassettes that mediate pulmonary cell- and lipid-sensitive pathways regulating surfactant homeostasis.

  10. Iportance of a functional catalytic cycle in lipid transport of ABCA3 suggestsa pathophysiological mechanism of pediatric intterstitial lung disease due to ABCA3 mutation.

ABCA3 profil antigène

Antigen Summary

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. The full transporter encoded by this gene may be involved in development of resistance to xenobiotics and engulfment during programmed cell death.

Gene names and symbols associated with ABCA3

  • ATP binding cassette subfamily A member 3 (ABCA3) anticorps
  • ABC transporter A family protein (abcA3) anticorps
  • ATP-binding cassette sub-family A member 3 (LOC100380656) anticorps
  • ATP-binding cassette sub-family A member 3 (LOC100484901) anticorps
  • ATP-binding cassette, sub-family A (ABC1), member 3 (Abca3) anticorps
  • ATP binding cassette subfamily A member 3 (Abca3) anticorps
  • ATP-binding cassette, sub-family A (ABC1), member 3b (abca3b) anticorps
  • ATP-binding cassette sub-family A member 3 (LOC101115674) anticorps
  • 1810036E22Rik anticorps
  • ABC-C anticorps
  • Abc3 anticorps
  • abca3 anticorps
  • DDBDRAFT_0201662 anticorps
  • DDBDRAFT_0219856 anticorps
  • DDB_0201662 anticorps
  • DDB_0219856 anticorps
  • EST111653 anticorps
  • LBM180 anticorps
  • si:ch211-155i15.6 anticorps
  • SMDP3 anticorps

Protein level used designations for ABCA3

ATP-binding cassette, sub-family A member 3 , ATP-binding cassette, sub-family A (ABC1), member 3 , ATP-binding cassette sub-family A member 3 , ATP-binding cassette sub-family A member 3-like , ABC transporter 3 , ABC-C transporter , ATP-binding cassette transporter 3

GENE ID SPECIES
453833 Pan troglodytes
479879 Canis lupus familiaris
696496 Macaca mulatta
8629224 Dictyostelium discoideum AX4
100345135 Oryctolagus cuniculus
100380656 Salmo salar
100484901 Ailuropoda melanoleuca
21 Homo sapiens
27410 Mus musculus
302973 Rattus norvegicus
416386 Gallus gallus
505787 Bos taurus
564344 Danio rerio
100402635 Callithrix jacchus
100518064 Sus scrofa
101115674 Ovis aries musimon
Fournisseurs de qualité sélectionnés pour ABCA3 (ABCA3) Kits ELISA
Avez-vous cherché autre chose?