LFNR1 Antibody

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Description

Introduction to IFNAR1 Antibody

IFNAR1 (Interferon Alpha Receptor 1) is a critical component of the type I interferon (IFN) receptor complex, mediating responses to IFN-α, IFN-β, and IFN-ω. IFNAR1 antibodies are tools or therapeutic agents designed to bind this receptor, modulating immune responses. These antibodies are used in research, diagnostics, and therapeutic development, particularly in viral infections, autoimmune diseases, and cancer.

Research Antibodies

Used in immunohistochemistry (IHC), flow cytometry, and Western blotting to study IFNAR1 expression and function.

Antibody TypeApplicationsSource
Rabbit PolyclonalIHC staining in HNSCC (head and neck squamous cell carcinoma) tissues .
Mouse MonoclonalFlow cytometry to assess IFNAR1 surface expression on immune cells .

Therapeutic Antibodies

Under investigation for immunomodulation in viral infections or autoimmune diseases.

MechanismExample Use Case
BlockadePreventing excessive IFN signaling in autoinflammatory diseases .
ActivationEnhancing antiviral responses in IFNAR1-deficient patients .

Role in Viral Immunity

  • IFNAR1 Deficiency: Linked to severe COVID-19, influenza pneumonia, and JEV (Japanese Encephalitis Virus) encephalitis. Patients with IFNAR1 mutations show impaired responses to IFN-α/ω but retain IFN-β responsiveness .

  • Antibody Utility: IFNAR1 antibodies enable detection of receptor expression levels in patient samples, aiding diagnostics .

Cancer and Immunotherapy

  • Immunosuppression: High IFNAR1 expression in HNSCC correlates with poor prognosis. IFNAR1 signaling promotes PDL1 upregulation, fostering immune evasion .

  • Therapeutic Target: Neutralizing IFNAR1 may restore antitumor immunity by reducing PDL1 expression .

Autoimmune and Inflammatory Diseases

  • Pathogenic Autoantibodies: Neutralizing anti-IFN antibodies (not anti-IFNAR1) are implicated in autoinflammatory syndromes .

  • Diagnostic Potential: IFNAR1 antibodies could identify dysregulated IFN signaling in lupus or rheumatoid arthritis.

Diagnostic Applications

MethodOutcomeSource
IHCQuantifies IFNAR1 expression in tumor biopsies; predicts prognosis in HNSCC .
Flow CytometryMeasures IFNAR1 on peripheral blood immune cells (e.g., CD8+ T cells, NK cells) .
ELISADetects soluble IFNAR1 or anti-IFNAR1 autoantibodies in serum .

Research Challenges

  1. Antibody Specificity: Cross-reactivity with homologous receptors (e.g., IFNAR2) requires rigorous validation .

  2. Standardization: Variability in IHC staining protocols across studies .

  3. Therapeutic Efficacy: Limited clinical data on IFNAR1-targeting therapies .

High-Throughput Screening

Projects like NeuroMab and PCRP emphasize rigorous antibody characterization via ELISA, immunohistochemistry, and Western blotting to ensure specificity .

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
LFNR1 antibody; PETH1 antibody; At5g66190 antibody; K2A18.27Ferredoxin--NADP reductase antibody; leaf isozyme 1 antibody; chloroplastic antibody; EC 1.18.1.2 antibody; Leaf FNR 1 antibody; AtLFNR1 antibody; FNR-1 antibody
Target Names
LFNR1
Uniprot No.

Target Background

Function
This antibody targets Ferredoxin-NADP+ reductase 1 (FNR1), a crucial enzyme in plant chloroplasts. FNR1 plays a vital role in regulating the balance between cyclic and non-cyclic electron flow, ensuring the plant's optimal production of ATP and reducing power.
Gene References Into Functions

Functional Studies of FNR1:

  • Oxidative Stress Response: In fnr1 knockout studies, NADP(H) and glutathione pools exhibit increased oxidation compared to wild-type plants, demonstrating the absence of photoprotective effects despite transcriptional evidence of oxidative stress. (PMID: 27634426)
  • Flowering Time Regulation: FNR1 serves as a key regulator of flowering time in response to nitrogen availability. (PMID: 27325772)
  • Post-Translational Regulation: The intricate regulatory mechanisms governing AtFNR highlight the complexity of chloroplast protein control through various post-translational modifications. (PMID: 25301888)
  • Photosynthetic Machinery and Photoprotection: FNR1 depletion leads to downregulation of the photosynthetic apparatus and the induction of photoprotective mechanisms. (PMID: 22300243)
  • Cyclic Electron Transfer: FNR1 mutants show increased cyclic electron transfer rates under standard growth conditions. (PMID: 19054362)
Database Links

KEGG: ath:AT5G66190

STRING: 3702.AT5G66190.1

UniGene: At.47570

Protein Families
Ferredoxin--NADP reductase type 1 family
Subcellular Location
Plastid, chloroplast stroma. Plastid, chloroplast thylakoid membrane; Peripheral membrane protein; Stromal side.
Tissue Specificity
Expressed in shoots. Restricted to green tissues, being more abundant in siliques.

Q&A

Here’s a structured collection of FAQs tailored for academic researchers working with L1 antibodies (assuming "LFNR1" refers to L1-related antibodies, as no direct references to "LFNR1" were found in the search results):

Advanced Research Questions

How to resolve contradictory data on L1’s role in tumor progression vs. neural repair?

  • Analytical framework:

    • Context-dependent analysis: Compare L1 isoforms (full-length vs. cleaved) using domain-specific antibodies (e.g., anti-Ig1-4 vs. anti-FnIII1-3) .

    • Use transcriptomic correlation (e.g., RNA-seq with L1 expression) to distinguish tumorigenic vs. neuroprotective pathways .

    • Example table for conflicting results:

ObservationPotential ExplanationValidation Method
High L1 in early-stage cancerImmune recognition of L1 antigensMeasure anti-L1 IgG titers
L1 promotes metastasisCleaved L1 fragments activate invasivenessUse cleavage-specific antibodies

How to design experiments probing L1’s dual role in immune activation and tumor evasion?

  • Experimental design:

    • Combine autoantibody detection (anti-ORF1p/ORF2p IgG ELISA) with immune profiling (e.g., PD-L1/CTLA-4 levels) in cancer cohorts .

    • Use bispecific antibodies to simultaneously target L1 and immune checkpoints (e.g., L1-CD3e engagers) .

What methods address L1 antibody cross-reactivity with embryonal or neuronal isoforms?

  • Solutions:

    • Employ tissue-specific blocking peptides during staining .

    • Use advanced epitope mapping (e.g., phage display libraries) to refine antibody specificity .

    • Validate in age-matched models to account for L1 expression in aging neurons .

Methodological Challenges & Troubleshooting

How to interpret variable anti-L1 antibody performance across cancer types?

  • Strategies:

    • Stratify by L1 derepression mechanisms (e.g., p53 status, hypomethylation) .

    • Compare antibody performance in 3D tumor spheroids vs. monolayer cultures to mimic in vivo heterogeneity .

What computational tools assist in L1 antibody engineering?

  • Resources:

    • RosettaAntibody for humanization and affinity maturation .

    • ABodyBuilder for predicting manufacturability risks (e.g., aggregation-prone regions) .

Key Data from Literature

L1 Antibody TargetFunctional ImpactRelevance to DiseaseSource
Ig-like domains 1–4Inhibits neurite outgrowthNeural injury, tumor invasion
FnIII domains 1–3Enhances cell migrationMetastatic cancers
ORF1p/ORF2pTriggers anti-L1 IgG responseEarly cancer detection

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