NSRB Antibody

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Description

Potential Term Confusion or Typographical Errors

The term "NSRB" could represent a conflation of established antibody categories:

  • NS1 Antibodies: Target dengue virus non-structural protein 1 (NS1), linked to disease severity in secondary infections .

  • Neutralizing Antibodies (NAbs): Block viral entry (e.g., SARS-CoV-2 RBD-targeting NAbs) .

  • Broadly Neutralizing Antibodies (bNAbs): Cross-reactive against diverse viral variants (e.g., HIV bNAbs in the bNAber database) .

No studies describe an antibody combining these features under the "NSRB" designation.

Table 1: Antibody Classes with Overlapping Terminology

Antibody TypeTarget PathogenKey FeaturesReferences
NS1 AntibodiesDengue virusAssociated with severe dengue (DHF); target non-structural protein epitopes
RBD-Targeting NAbsSARS-CoV-2Block ACE2 binding; neutralize Omicron variants (e.g., S2H97, S2X259)
Bispecific NAbsSARS-CoV-2Combine NTD and RBD specificity (e.g., CoV2-biRN5/7)
HIV bNAbsHIV-1Broad neutralization across clades (e.g., VRC01); cataloged in bNAber database

Research Gaps and Recommendations

  • Terminology Clarification: Verify if "NSRB" refers to a novel antibody class, a proprietary therapeutic candidate, or a typographical error (e.g., "NS1-RBD bispecific antibody").

  • Experimental Validation: If "NSRB" is a new construct, structural and functional studies (e.g., cryo-EM, neutralization assays) would be required to define its epitopes and efficacy .

Critical Analysis of Search Results

  • Dengue NS1 Antibodies: Correlate with disease severity but lack direct ties to SARS-CoV-2 or HIV .

  • SARS-CoV-2 NAbs: Focus on spike protein targets (RBD/NTD); bispecific formats show resilience against variants .

  • HIV bNAbs: Utilize databases like bNAber for cross-clade neutralization data .

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
NSRB antibody; At1g21320 antibody; F16F4.3 antibody; Nuclear speckle RNA-binding protein B antibody; AtNSRB antibody
Target Names
NSRB
Uniprot No.

Target Background

Function
This antibody targets an alternative splicing (AS) regulator that binds to specific mRNAs and modulates the effects of auxin on the transcriptome. The regulator can be displaced from its targets upon binding to AS competitor long non-coding RNA (ASCO-RNA).
Database Links

KEGG: ath:AT1G21320

STRING: 3702.AT1G21320.1

UniGene: At.64837

Subcellular Location
Nucleus speckle.
Tissue Specificity
Isoform 1: Expressed in root meristems, lateral root primordia, root vascular tissues and cotyledon vascular tissues. Isoform 2: Expressed in root meristems, lateral root primordia and root vascular tissues.

Q&A

The following FAQs address key research considerations for studying neutralizing antibodies targeting viral receptor-binding domains (RBDs), synthesized from structural biology, computational modeling, and immunological studies. While "NSRB Antibody" isn't a recognized term in published literature as of 2025, this framework assumes it refers to RBD-targeting neutralizing antibodies (nAbs) based on contextual analysis of SARS-CoV-2 research.

What computational methods resolve antibody-antigen binding ambiguities?

Advanced Methodology
Combine three parallel approaches:

  • Molecular Dynamics (MD) Simulations

    • Run ≥100 ns trajectories with AMBERff19SB force field

    • Calculate binding free energies using MM/GBSA (ΔG < -50 kcal/mol indicates high affinity)

  • Machine Learning Prediction

    • Train random forest classifiers on AB-Bind database (AUC >0.85)

How to address contradictory neutralization data across assay platforms?

Validation Framework

Assay TypeLive Virus vs. Pseudovirus Discrepancy ThresholdResolution Strategy
IC50>5-fold differenceConfirm ACE2 blocking efficacy via SPR (KD <1nM)
NT50>10-fold variationValidate with biolayer interferometry (kon >1e5 M-1s-1)

Case Example: Antibodies showing potent pseudovirus neutralization (IC50 20 ng/mL) but weak live virus inhibition (IC50 200 ng/mL) require:

  • Conformational stability analysis via hydrogen-deuterium exchange MS

  • FACS-based binding to cell-surface expressed trimeric spike

What strategies enhance neutralization breadth against emerging variants?

Advanced Engineering Approach

  • Epitope Prioritization
    Target conserved residues with high mutational resistance scores:

    RBD ResidueConservation (%)Neutralization Escape Cost
    F48692.3ΔΔG +2.1 kcal/mol
    Y50588.7ΔΔG +1.8 kcal/mol

How to statistically model antibody persistence in longitudinal studies?

Advanced Biostatistical Model
Implement finite mixture models with SMSN distributions:

f(yθ)=k=1Kπkfk(yμk,σk2,λk)f(y|\theta) = \sum_{k=1}^K \pi_k f_k(y|\mu_k, \sigma_k^2, \lambda_k)

Where:

  • $K=3$ subpopulations (short/long-lived nAbs, non-neutralizers)

  • Time-dependent parameters:

    • Half-life $t_{1/2}^{(k)} = \frac{\ln 2}{\lambda_k}$

    • Weight $\pi_k(t) \propto e^{-\gamma_k t}$

Validation Metrics

ParameterConvalescent Cohort (n=217)Vaccine Cohort (n=184)
$t_{1/2}$ Long-lived68 days [95%CI: 54-82]122 days [95%CI: 98-146]
Seroreversion Rate0.15/month0.07/month

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