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Human IgA Single Plex Kit (Flow Cytometry Bead Assay)

Human IgA Single Plex Kit (Flow Cytometry Bead Assay)

Catalog Number: S0Q3043 Reactivity: Human Conjugation: Brand: Starter
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Regular price $500 USD
Regular price Sale price $500 USD
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Product Details

Product Specification


Antigen Human IgA
Reactivity Human
Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8°C as supplied.

Kit


Precision Intra-assay:;
Inter-assay:
Sample type Serum; Plasma-EDTA; Plasma-Heparin; Plasma-Citrate; Cell Culture Supernatant
Assay type Sandwich (quantitative)
Sensitivity 0.069 ng/mL
Range 0.30 ng/mL-220 ng/mL
Recovery Serum: 101.79%
Plasma-EDTA:99.51%
Plasma-Heparin:98.64%
Plasma-Citrate:100.61%
Cell culture supernatant: 100.68%
Assay time 70 minutes
Species reactivity Human

Background

Immunoglobulin A (IgA) is a critical antibody isotype central to mucosal immunity and systemic immune regulation. Structurally, IgA exists in two primary forms: monomeric IgA in serum (predominantly IgA1) and dimeric or polymeric secretory IgA (sIgA) at mucosal surfaces. Each IgA molecule comprises two α-heavy chains and two light chains (κ or λ), forming a flexible Y-shaped structure stabilized by disulfide bonds. The α-heavy chain contains three constant domains (Cα1–Cα3), with the Fc region (Cα2–Cα3) facilitating interactions with Fcα receptors (FcαRI) and the polymeric immunoglobulin receptor (pIgR). Secretory IgA incorporates a J-chain and a secretory component, which enhance its stability in protease-rich mucosal environments. Extensive glycosylation of IgA further modulates its solubility, receptor binding, and resistance to microbial degradation. IgA is the predominant antibody at mucosal surfaces (e.g., respiratory, gastrointestinal, and urogenital tracts), where it neutralizes pathogens, prevents microbial adherence, and regulates commensal microbiota. Secretory IgA mediates immune exclusion by trapping pathogens in mucus for mechanical clearance, while serum IgA contributes to systemic immune regulation by dampening inflammatory responses via FcαRI signaling. Additionally, IgA engages in eosinophil-mediated antiparasitic defense and modulates allergic reactions through interactions with immune cells. Human IgA shares conserved structural motifs with IgA from primates and rodents, particularly in the α-chain constant domains. However, species-specific variations in glycosylation patterns, J-chain association, and secretory component binding necessitate species-specific detection assays. For instance, human IgA1’s unique hinge region, rich in proline and O-glycosylation sites, distinguishes it from murine IgA, which lacks this feature. Applications of the Human IgA ELISA Kit: This OneStep Human IgA ELISA kit enables rapid, accurate quantification of IgA in serum, plasma, or cell culture supernatants. Advantages of this OneStep ELISA Kit Design: Simplified Workflow: Combines sample incubation and detection in a single step, eliminating intermediate washing and reducing hands-on time. High Efficiency: Achieves results within 1 hours, ideal for high-throughput studies or urgent diagnostics. Enhanced Precision: Minimizes procedural variability and cross-contamination risks through optimized reagent formulation. Broad Compatibility: Validated for diverse biological matrices, ensuring flexibility in experimental design. This kit’s streamlined protocol and robust performance make it an indispensable tool for researchers and clinicians seeking reliable IgA quantification in time-sensitive or resource-limited settings.

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CBA

Standard curve

Example of IgA standard curve in Assay Diluent .

Dilution Parallelism

Pre-diluted serum and plasma (EDTA, Heparin, Citrate) samples (1:40,000 in sample diluent) and cell culture supernatant (labeled as "Undiluted") were further serially diluted 2X, and 4X with sample diluent and assayed for Human IgA. Data shown on the y-axis represent the measured Human IgA concentrations multiplied by their respective serial dilution factors (ng/mL)

Accuracy and Spike Recovery

Serum and plasma (EDTA, Heparin, Citrate) matrices—pre-diluted at the minimum sample dilution (MSD = 1:40,000) in sample diluent and immunodepleted with target-specific magnetic beads to near the lower limit of linearity—along with cell culture supernatant (Supernatant), were spiked with high, medium, and low levels of Human IgA. The y-axis displays the calculated spike recovery percentages (Spike Recovery%), with values across all tested matrices ranging between 80% and 120%.

Sample Reactivity
Serum and plasma (EDTA, Heparin, Citrate) samples from human, mouse (CK), and rat (SD) were diluted at the minimum sample dilution (MSD = 1:40,000) and assayed for Human IgA (ng/mL). Measurable concentrations were detected in human samples, whereas all mouse and rat samples yielded values of 0 ng/mL.

Protocol Diagram