pas-1 Antibody

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Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
pas-1 antibody; C15H11.7Proteasome subunit alpha type-6 antibody; EC 3.4.25.1 antibody; Proteasome subunit alpha 1 antibody
Target Names
pas-1
Uniprot No.

Target Background

Function
The proteasome is a multi-catalytic proteinase complex. It is characterized by its ability to cleave peptides with Arg, Phe, Tyr, Leu, and Glu residues adjacent to the leaving group at neutral or slightly basic pH. The proteasome exhibits ATP-dependent proteolytic activity.
Database Links

KEGG: cel:CELE_C15H11.7

STRING: 6239.C15H11.7.2

UniGene: Cel.2930

Protein Families
Peptidase T1A family
Subcellular Location
Cytoplasm. Nucleus.

Q&A

Here’s a structured collection of academic research-focused FAQs for PAS-1 antibody studies, incorporating methodological guidance and evidence-based insights:

Advanced Research Questions

How to resolve contradictory data on PAS-1’s immunosuppressive mechanisms?

  • Approach:

    • Replicate cytokine profiling (e.g., IL-10, TGF-β, IFN-γ) across multiple models (murine asthma, OVA-induced inflammation) .

    • Compare T-cell subsets (CD4+ CD25+ FoxP3+ vs. CD8+ γδTCR+) in adoptive transfer experiments .

    • Validate findings using dual RNA-seq and flow cytometry to track PAS-1-responsive immune pathways .

What in vivo experimental designs capture PAS-1’s dose-dependent effects?

  • Protocol:

    • Administer PAS-1 (1–100 μg/mouse) during OVA sensitization .

    • Measure outcomes:

      • IgE/IgG1 suppression .

      • Eosinophil peroxidase levels in bronchoalveolar lavage .

      • Airway hyperreactivity via pulmonary mechanics .

    • Include IL-4/IL-13 knockout models to isolate Th2-independent effects .

How does PAS-1 modulate cross-talk between dendritic cells and Tregs?

  • Mechanistic analysis:

    • Isolate splenic dendritic cells post-PAS-1 exposure .

    • Assess MHC-II and CD86 expression via flow cytometry .

    • Co-culture with naïve T-cells ± IL-10/TGF-β neutralizing antibodies .

Data Interpretation Challenges

Discrepancies in PAS-1’s inhibition of IgE vs. IgG2a: Methodological insights

  • Hypothesis testing:

    • Variable: Antigen type (T-cell-dependent vs. independent) .

    • Controls:

      • Use OVA (T-dependent) and NP-Ficoll (T-independent) .

      • Quantify B-cell activation markers (CD69/CD86) via flow cytometry .

Standardizing PAS-1 purity for reproducible immunomodulation studies

  • Quality checks:

    • SDS-PAGE analysis to confirm 200 kDa band .

    • Endotoxin testing (<0.1 EU/μg via LAL assay) .

    • Functional validation: Suppression of OVA-specific DTH reactions .

Emerging Research Frontiers

Can PAS-1’s immunosuppressive motifs be engineered into therapeutic antibodies?

  • Design strategy:

    • Map PAS-1 epitopes recognized by MAIP-1 monoclonal antibody .

    • Fuse bioactive regions (e.g., IL-10-inducing domains) with IgG Fc .

    • Test chimeric antibodies in autoimmune models (e.g., EAE, IBD) .

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