ATL11 Antibody

Shipped with Ice Packs
In Stock

Description

Antibodies in ATL Research and Therapy

ATL is an aggressive T-cell malignancy caused by human T-lymphotropic virus type 1 (HTLV-1). Antibodies play critical roles in diagnostics, pathogenesis studies, and targeted therapies for ATL. Key antibody classes include:

Anti-CCR4 Antibodies (e.g., Mogamulizumab)

  • Target: CC chemokine receptor 4 (CCR4), highly expressed on ATL cells and HTLV-1-infected T cells .

  • Mechanism: Antibody-dependent cellular cytotoxicity (ADCC) via defucosylated Fc regions enhances immune cell-mediated tumor lysis .

  • Clinical Efficacy:

    • Phase II trials: 30–50% response rates in relapsed ATL patients .

    • Proviral load reductions: Up to 2-log decreases in chronic ATL subtypes .

Anti-CD25 Antibodies (e.g., Daclizumab)

  • Target: Interleukin-2 receptor α-chain (CD25), overexpressed in ATL .

  • Outcomes: Limited efficacy as monotherapy but synergistic with agents like pentostatin .

Anti-CD52 Antibodies (Alemtuzumab)

  • Target: CD52, expressed on lymphocytes.

  • Application: Reduces HTLV-1 viral load and restores normal T-cell counts in combination therapies .

Antibodies for Biomarker Detection

  • MT-1 Cell Antigen: Detected via indirect immunofluorescence in 26% of healthy adults in ATL-endemic regions, suggesting subclinical HTLV-1 infections .

  • TCRVβ Staining: Identifies clonal T-cell expansions in ATL patients, aiding malignancy diagnosis .

Functional Characterization

  • Neutralization: Antibodies block viral entry or oncoprotein signaling (e.g., Tax protein) .

  • Immune Recruitment: Antibodies tag ATL cells for phagocytosis or complement-mediated lysis .

Comparative Efficacy of ATL-Targeted Antibodies

AntibodyTargetMechanismClinical PhaseResponse RateKey Study Findings
MogamulizumabCCR4ADCC enhancementPhase II30–50%2-log PVL reduction in chronic ATL
DaclizumabCD25IL-2 receptor blockadePhase I/II<20%Synergy with pentostatin
AlemtuzumabCD52Lymphocyte depletionPreclinicalN/AReduces HTLV-1 load in models

Recombinant Antibody Engineering

  • IgG Subclass Switching: Enhances effector functions (e.g., ADCC) while retaining antigen specificity .

  • Validation Pipelines: High-throughput screening (e.g., NeuroMab’s ELISA/immunofluorescence protocols) improves antibody reliability .

Limitations

  • Heterogeneity: ATL clones exhibit variable antigen expression, complicating antibody targeting .

  • Resistance: Mutations in CCR4 (e.g., C-terminal truncations) reduce therapeutic efficacy .

Key Research Findings

Study FocusMethodologyKey OutcomeSource
Mogamulizumab in ATLPhase II trial30–50% response rate in relapsed patients
TCRVβ clonal detectionFlow cytometry100% specificity for malignant ATL clones
MT-1 antigen prevalenceSerological screening26% positivity in endemic healthy adults

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
14-16 week lead time (made-to-order)
Synonyms
ATL11; At1g72200; T9N14.11; RING-H2 finger protein ATL11; RING-type E3 ubiquitin transferase ATL11
Target Names
ATL11
Uniprot No.

Target Background

Database Links

KEGG: ath:AT1G72200

STRING: 3702.AT1G72200.1

UniGene: At.35131

Protein Families
RING-type zinc finger family, ATL subfamily
Subcellular Location
Membrane; Single-pass membrane protein.

Q&A

Given the lack of specific information on "ATL11 Antibody" in the search results, I will create a general FAQ for researchers based on common antibody-related research scenarios, focusing on experimental design, data analysis, and methodological considerations. This approach will ensure the FAQs are relevant to academic research and cover both basic and advanced questions.

A:

To validate the specificity of a new antibody, follow these steps:

  • Western Blotting: Use Western blotting to assess the antibody's ability to recognize its target protein in cell lysates. Include controls with known positive and negative samples.

  • Immunofluorescence or Immunohistochemistry: Perform immunofluorescence or immunohistochemistry to visualize the protein's localization in cells or tissues.

  • Flow Cytometry: If applicable, use flow cytometry to analyze cell surface protein expression.

  • Blocking Experiments: Conduct blocking experiments with the antigen or a competing antibody to confirm specificity.

A:

  • Data Replication: Ensure that results are reproducible across multiple experiments.

  • Control Experiments: Include appropriate controls to validate the findings.

  • Statistical Analysis: Use statistical methods to compare results between different conditions.

  • Literature Review: Compare your findings with existing literature to identify potential discrepancies and explanations.

A:

  • Specificity and Sensitivity: Choose antibodies with high specificity and sensitivity for the target antigen.

  • Cross-reactivity: Assess potential cross-reactivity with other proteins.

  • Concentration and Buffer Conditions: Optimize antibody concentration and buffer conditions for the specific application.

  • Species and Isotype: Ensure the antibody is suitable for the species and application (e.g., mouse vs. human).

A:

  • Multiplexing: Use multiple antibodies in a single experiment to analyze several proteins simultaneously.

  • Combination with Other Techniques: Combine antibodies with techniques like mass spectrometry or CRISPR-Cas9 for enhanced protein analysis.

  • Bispecific Antibodies: Utilize bispecific antibodies to engage multiple targets or cell types.

A:

  • Antibody Validation: Validate antibodies using multiple methods to ensure specificity and efficacy.

  • Sample Preparation: Ensure proper sample preparation to maintain protein integrity.

  • Experimental Controls: Include appropriate controls to account for non-specific binding or background signals.

  • Data Documentation: Maintain detailed records of experimental conditions and results for reproducibility.

A:

  • Non-specific Binding: Use blocking agents or optimize antibody concentrations to reduce non-specific binding.

  • Low Signal: Enhance signal by optimizing antibody concentrations, using amplification steps, or improving detection methods.

  • Background Noise: Minimize background by optimizing washing steps and using appropriate controls.

A:

  • Antibody Engineering: Develop engineered antibodies with improved specificity, affinity, or functionality.

  • Single-Cell Analysis: Apply antibodies in single-cell analysis techniques to study cellular heterogeneity.

  • Therapeutic Applications: Explore antibodies as therapeutic agents in various diseases.

Quick Inquiry

Personal Email Detected
Please use an institutional or corporate email address for inquiries. Personal email accounts ( such as Gmail, Yahoo, and Outlook) are not accepted. *
© Copyright 2025 TheBiotek. All Rights Reserved.