FAS2 Antibody

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Description

Introduction to Fas2 Antibody

Fas2 antibodies target the Fasciclin 2 protein, an evolutionarily conserved cell adhesion molecule. In Drosophila melanogaster, Fas2 is the orthologue of mammalian neural cell adhesion molecule (NCAM) and regulates neural development, epithelial morphogenesis, and EGFR signaling . In parasitology, Fas2 refers to a Fasciola hepatica-derived antigen used in immunodiagnostic assays for detecting human and animal fascioliasis .

Biological Roles

  • Neural Development: Fas2 mediates axon guidance and synaptic plasticity via homophilic adhesion .

  • EGFR Regulation: Fas2 inhibits EGFR signaling during eye, wing, and notum development, with loss-of-function mutants showing hyperactive EGFR phenotypes .

  • Isoform Diversity: Fas2 has seven isoforms, including GPI-anchored and transmembrane variants. Secreted isoforms can rescue lethality in Fas2 mutants, suggesting non-adhesive signaling roles .

Key Antibodies

CloneTarget RegionApplicationsHost SpeciesSupplierReferences
34B3Extracellular domainsWB, IHC, IF, IPMouseDSHB
1D4Extracellular domainsIF, IHC, Neuronal stainingMouseLabome
Fas2-YFPFull-length isoformsRescue experimentsN/AGenetic constructs

Fas2 as a Diagnostic Tool in Parasitology

Fas2-ELISA detects IgG antibodies against Fasciola hepatica cysteine proteinase Fas2, offering high sensitivity and specificity in endemic regions .

Performance Metrics

Study LocationSensitivity (%)Specificity (%)Population SizeReference
Peruvian Andes92.483.6634 children
Peruvian Andes95.586.6664 children
  • Advantages: Rapid seroconversion (1–2 weeks post-infection) and high negative predictive value (97.2%) .

  • Limitations: No correlation between antibody levels and infection intensity .

In Drosophila

  • Fas2 loss disrupts epithelial integrity, causing "popped-out" cells in ovarian follicles .

  • Secreted Fas2 rescues Fas2 mutant lethality without homophilic adhesion, implying receptor-mediated signaling .

  • Fas2 interacts with Ephrin signaling pathways to regulate photoreceptor morphogenesis .

In Parasitology

  • Fas2-ELISA outperforms coprological methods in early detection, critical for managing outbreaks .

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
14-16 weeks (Made-to-order)
Synonyms
FAS2 antibody; NFB1 antibody; At5g64630 antibody; MUB3.9Chromatin assembly factor 1 subunit FAS2 antibody; CAF-1 subunit FAS2 antibody; CAF-1 p60 homolog antibody; Protein FASCIATA 2 antibody
Target Names
FAS2
Uniprot No.

Target Background

Function
This antibody targets FAS2, a component of the chromatin assembly factor 1 (CAF-1) complex. CAF-1 plays a crucial role in chromatin assembly following DNA replication and repair. FAS2 is essential for various developmental processes, including seedling growth and leaf trichome differentiation. It is critical for maintaining the organization of the shoot apical meristem (SAM) and root apical meristem (RAM) during post-embryonic development by stabilizing gene expression patterns. While not essential for maintaining the transcriptional repression of heterochromatic genes, FAS2 is involved in homologous recombination.
Gene References Into Functions
  • Mutations in FAS1 and FAS2 result in a progressive reduction of telomeric and 45S rDNA repeats. PMID: 20699390
  • CAF-1 ensures the stable inheritance of epigenetic states throughout Arabidopsis growth and development. PMID: 16436052
  • Studies indicate that the CAF-1 complex, including FAS2, functions in heterochromatin formation. PMID: 16452472
  • FAS2 depletion significantly increases (approximately 40-fold) the frequency of somatic homologous recombination (HR) in plants. PMID: 17110925
Database Links

KEGG: ath:AT5G64630

STRING: 3702.AT5G64630.2

UniGene: At.28741

Protein Families
WD repeat HIR1 family
Subcellular Location
Nucleus.

Q&A

What is the role of FAS2 in Fasciola hepatica infection diagnosis, and how does it compare to other diagnostic methods?

FAS2, a cysteine proteinase from Fasciola hepatica, is used in the FAS2-ELISA assay for diagnosing fascioliasis. This assay exhibits high sensitivity and specificity, making it effective for detecting infections in endemic areas . Compared to other methods, FAS2-ELISA offers a specific and early detection of infection, which is crucial for timely treatment . Other diagnostic methods include coprology and imaging techniques, but FAS2-ELISA provides a more rapid and serological approach.

How does the FAS2 antigen interact with IgM and IgG antibodies in the context of Fasciola hepatica infection?

In Fasciola hepatica infections, the FAS2 antigen interacts with both IgM and IgG antibodies. IgG antibodies are detected using the FAS2-ELISA, which is highly specific and sensitive for diagnosing chronic infections . IgM antibodies, detected via IgM-ELISA, are indicative of the acute phase of infection, providing a specific marker for early detection . This dual approach allows researchers to monitor the progression of the disease.

What are the methodological considerations for using FAS2-ELISA in field screenings versus clinical settings?

When using FAS2-ELISA in field screenings, considerations include the need for portable equipment and rapid results. In clinical settings, the assay can be more thoroughly validated with additional diagnostic tools. Field screenings often require higher throughput and simpler protocols, while clinical settings allow for more detailed analysis and confirmation of results .

What are the potential challenges and limitations of using FAS2-ELISA for diagnosing fascioliasis in diverse populations?

Challenges include variability in immune responses among different populations, potential cross-reactivity with other parasites (although FAS2-ELISA shows no cross-reactivity with common parasites) , and the need for standardized protocols across different laboratories. Additionally, the sensitivity and specificity may vary slightly depending on the population studied .

How can researchers address data contradictions or inconsistencies in FAS2 antibody studies?

Addressing data contradictions involves reviewing experimental design, ensuring consistent antigen preparation, and validating results across multiple studies. It is also crucial to consider factors like sample size, population demographics, and the timing of sample collection relative to infection onset. Meta-analyses and systematic reviews can help reconcile discrepancies by synthesizing data from multiple studies.

What are the implications of FAS2 antibody research for the development of new diagnostic tools or therapeutic strategies against fascioliasis?

Research on FAS2 antibodies contributes significantly to the development of more accurate and early diagnostic tools for fascioliasis. This can lead to better disease management by enabling early treatment, reducing liver damage, and improving outcomes in endemic areas. Additionally, understanding the immune response to FAS2 may inform the development of vaccines or targeted therapies against Fasciola hepatica.

How does the use of FAS2-ELISA compare to other serological tests for detecting parasitic infections, such as those caused by Schistosoma or Paragonimus?

FAS2-ELISA is highly specific for Fasciola hepatica and does not cross-react with other common parasites like Schistosoma mansoni or Paragonimus westermani . This specificity makes it a valuable tool in areas where multiple parasitic infections are endemic. Other serological tests may have different specificities and sensitivities depending on the target parasite.

What are the key factors influencing the sensitivity and specificity of FAS2-ELISA in different study populations?

Key factors include the prevalence of infection, the timing of sample collection relative to infection onset, the quality of antigen preparation, and the population's immune response variability. Additionally, the assay's performance can be influenced by the presence of other infections or conditions that might affect immune responses.

How can researchers optimize the FAS2-ELISA protocol for improved performance in resource-limited settings?

Optimization involves simplifying the protocol, reducing reagent costs, and ensuring that the assay can be performed with minimal equipment. This might include using dried blood spots for sample collection and developing a more rapid, point-of-care version of the assay. Collaboration with local health authorities and laboratories can help adapt the protocol to specific resource constraints.

Data Table: Diagnostic Parameters of FAS2-ELISA

Diagnostic ParameterValuePopulation Studied
Sensitivity95%Infected Individuals
Specificity100%Healthy Volunteers
Cross-reactivityNoneOther Parasitic Infections
Sample Size38 Infected, 46 HealthyAdults and Children in Endemic Areas

Future Directions

  • Vaccine Development: Understanding immune responses to FAS2 could inform vaccine strategies.

  • Therapeutic Targets: FAS2 may serve as a target for developing new treatments against Fasciola hepatica.

  • Point-of-Care Diagnostics: Simplifying FAS2-ELISA for use in field settings could enhance disease surveillance and management.

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