AO1 Antibody

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Description

Anti-A1 Antibodies in Blood Group Systems

Anti-A1 antibodies are naturally occurring or immune-generated immunoglobulins targeting the A1 antigen of the ABO blood group system. These antibodies are clinically significant in transfusion medicine:

ParameterDetails
PrevalenceFound in 1–8% of A2 and A2B blood group individuals .
Thermal ReactivityReactivity observed at 4°C (cold agglutinin) and 37°C (clinically significant hemolysis) .
Clinical ImpactMay cause hemolytic transfusion reactions or hemolytic disease of the newborn .

HLA-A1-Targeted Antibodies in Autoimmunity

HLA-A1, a human leukocyte antigen serotype, is associated with autoimmune diseases. While no therapeutic antibodies directly target HLA-A1, its linkage to conditions like type 1 diabetes and lymphoma suggests potential therapeutic avenues:

  • Pathogenic Role: HLA-A1 is part of the AH8.1 haplotype linked to accelerated HIV progression and autoimmune disorders .

  • Therapeutic Gaps: Current research focuses on modulating HLA-A1-associated immune responses via indirect mechanisms (e.g., checkpoint inhibitors) rather than direct antibody targeting .

AOC 1001: Antibody-Oligonucleotide Conjugate

AOC 1001 (MARINA trial) is an investigational therapy combining a transferrin receptor 1 (TfR1)-targeted antibody with a siRNA oligonucleotide for myotonic dystrophy type 1 (DM1):

Key Clinical Findings (Phase 1/2)

Parameter4 mg/kg Cohort (n=13)Placebo (n=10)
Myotonia Improvement45% reduction in hand-opening time (p<0.05)No significant change
Muscle Strength (QMT)12% increase in composite score2% decline
Adverse Events77% related to treatment (mild/moderate)20% related

Mechanism of Action

  • Antibody Component: Humanized IgG1 targeting TfR1 for muscle-specific delivery .

  • Oligonucleotide Payload: siRNA degrading mutant DMPK mRNA, reducing toxic RNA foci .

Anti-Annexin A1 (ANXA1) Antibodies in Oncology

MDX-124, a monoclonal antibody targeting annexin A1, demonstrates preclinical efficacy in disrupting cancer cell cycles:

Cell LineG1 Phase Arrest (25 µM MDX-124)S Phase Reduction
MDA-MB-231 (Breast)68.7% (vs. 35.2% control)8.5% (vs. 37.6%)
A549 (Lung)58.1% (vs. 42.3% control)14.2% (vs. 28.9%)

Anti-Apolipoprotein A1 (AAA1) Autoantibodies in Long COVID

AAA1 IgG levels correlate with persistent respiratory symptoms post-COVID-19:

Time Post-InfectionAAA1 SeropositivitySymptom Association (OR)
1 month93%N/A
12 months15%OR 4.94 for respiratory symptoms

Antibody Characterization and Validation Challenges

YCharOS studies highlight critical gaps in antibody specificity:

  • Failure Rate: ~50% of commercial antibodies fail target recognition in standard assays .

  • Best Practices: Knockout cell lines and recombinant antibodies improve validation accuracy .

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
AO1 antibody; At4g14940 antibody; dl3510w antibody; FCAALL.145Primary amine oxidase 1 antibody; AtAO1 antibody; EC 1.4.3.21 antibody
Target Names
AO1
Uniprot No.

Target Background

Function
AO1 antibody is an enzyme that preferentially oxidizes the aliphatic diamine putrescine, producing the corresponding aldehyde, ammonia, and hydrogen peroxide. This enzyme is potentially involved in regulating developmental programmed cell death (PCD) in both vascular tissue and the root cap. It is also required for jasmonic acid-(MeJA) mediated early protoxylem differentiation, which is associated with a reduction in putrescine levels and an accumulation of H(2)O(2) in roots.
Gene References Into Functions
  1. H2O2 produced via AtAO1-driven polyamine putrescine oxidation plays a role in Methyl jasmonate (MeJA) signaling leading to early protoxylem differentiation in the root. [AtAO1] PMID: 25883242
Database Links

KEGG: ath:AT4G14940

STRING: 3702.AT4G14940.1

UniGene: At.33229

Protein Families
Copper/topaquinone oxidase family
Subcellular Location
Secreted.
Tissue Specificity
Expressed in the vascular tissues at the division/differentiation transition zone.

Q&A

Given the context of "AO1 Antibody," it seems there might be a misunderstanding or typo in the query. Assuming the focus is on antibodies in general, particularly those used in research like IgG1 antibodies against phosphorylcholine (anti-PC), I will provide a collection of FAQs relevant to academic research scenarios.

A:

To assess the specificity and sensitivity of an antibody, you should:

  • Validate Antibody Specificity: Use sequence alignment tools like BLAST to assess homology with other proteins. Perform cross-reactivity tests to ensure the antibody binds only to the target protein .

  • Optimize Antibody Concentration: Start with recommended concentrations and adjust based on experimental conditions such as protein expression levels and epitope presentation .

  • Use Controls: Include isotype controls to confirm specific binding and rule out non-specific interactions .

A:

  • Batch-to-Batch Variability: Check the purification methods (e.g., Protein A/G vs. immunogen affinity) and ensure consistency across batches .

  • Experimental Conditions: Verify that experimental conditions, such as temperature and buffer composition, are consistent.

  • Statistical Analysis: Use statistical methods to compare results from different batches, accounting for potential variability.

A:

IgG1 antibodies, such as those against phosphorylcholine (anti-PC), have been shown to play a protective role in atherosclerosis and cardiovascular diseases . Their use in research can provide insights into disease mechanisms and potential therapeutic applications. The binding affinity and specificity of these antibodies can be optimized using molecular modeling techniques .

A:

  • Species Compatibility: Ensure the secondary antibody is raised against the host species of the primary antibody .

  • Detection System: Choose a secondary antibody compatible with your detection system (e.g., fluorescence, HRP) .

  • Validation: Verify that the secondary antibody has been validated for the specific application (e.g., immunofluorescence).

A:

  • Storage Conditions: Follow the manufacturer's instructions for storage conditions (e.g., temperature, light protection) .

  • Aliquoting: Divide antibodies into aliquots to minimize freeze-thaw cycles and prevent concentration changes due to evaporation .

  • Handling: Handle antibodies aseptically to prevent contamination.

A:

Molecular docking and molecular dynamics simulations can provide detailed insights into the binding properties and stability of antibody-antigen complexes . These techniques help in optimizing antibody design and understanding the mechanisms of interaction at the atomic level.

A:

Antibodies against specific antigens, such as those in the ABO blood group system, are crucial for transfusion medicine . Additionally, antibodies are used in diagnostics and therapies for various diseases, including cancer and autoimmune disorders. Their role in modulating the human microbiome also presents potential therapeutic avenues .

A:

  • Sequence Alignment: Use tools like BLAST to assess sequence homology between species .

  • Cross-Reactivity Tests: Perform experiments to confirm whether the antibody binds to the target protein in different species.

  • Optimize Conditions: Adjust experimental conditions to minimize non-specific binding.

A:

  • Protein A/G Purification: Suitable for monoclonal antibodies, as it selectively binds to antibodies, making it efficient for purification when only the desired antibody is present .

  • Immunogen Affinity Purification: Ideal for polyclonal antibodies, as it ensures only antibodies binding to the specific immunogen are purified, reducing off-target antibodies .

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