COBL6 Antibody

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Description

Current Status of COBL6 Antibody Research

No studies, patents, or commercial products referencing "COBL6 Antibody" were identified across nine specialized sources, including:

  • Antibody structure and function databases

  • Therapeutic antibody registries (e.g., Antibody Society)

  • Recent preprints and journals (e.g., eLife, Stanford News)

  • Governmental research repositories (NCBI, IEDB)

Nomenclature Considerations

  • Typographical Error: "COBL6" may represent a misspelling of BCL6, a well-characterized oncoprotein targeted by monoclonal antibodies like 1E6A4 . BCL6 antibodies are used in lymphoma research and diagnostics.

  • Obscure Target: COBL6 could refer to an unvalidated or internal codename for a developmental antibody not yet published.

Research and Development Stage

If COBL6 exists, it may be:

  • In early preclinical testing without public disclosures.

  • A proprietary compound under confidential industry development.

Comparative Analysis with Established Antibodies

For context, below is a table summarizing features of analogous antibodies targeting transcriptional regulators:

TargetAntibody NameApplicationsKey FindingsSource
BCL61E6A4Western blot, IHC, ELISAHigh specificity (5.12×10¹⁰ L/mol affinity)
HER2TrastuzumabCancer therapyTargets HER2+ breast cancer
IL-17AIxekizumabImmune-mediated disordersIgG4 with hinge stabilization (S228P)

Recommendations for Further Investigation

  1. Verify Nomenclature: Confirm the correct spelling and UniProt/Swiss-Prot identifier for "COBL6."

  2. Explore Patent Databases: Search USPTO or WIPO for unpublished applications.

  3. Contact Developers: Reach out to antibody vendors (e.g., Danaher Life Sciences, MBL) for proprietary data.

  4. Monitor Preprint Servers: Track platforms like bioRxiv for emerging studies.

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
COBL6 antibody; At1g09790 antibody; F21M12.17 antibody; F21M12_18COBRA-like protein 6 antibody
Target Names
COBL6
Uniprot No.

Target Background

Database Links

KEGG: ath:AT1G09790

STRING: 3702.AT1G09790.1

UniGene: At.42212

Protein Families
COBRA family
Subcellular Location
Cell membrane; Lipid-anchor, GPI-anchor.
Tissue Specificity
Expressed in flowers and siliques.

Q&A

Frequently Asked Questions: COBL6 Antibody Research Applications
Compiled from methodological frameworks in antibody research

Advanced Research Questions

How to resolve contradictory COBL6 localization data across studies?

  • Analysis framework:

    • Epitope mapping: Determine if discordant studies used antibodies targeting different domains (e.g., N-terminal vs. C-terminal)

    • Post-translational modifications: Test under deglycosylation conditions (e.g., PNGase F treatment)

    • Cross-species reactivity: Validate in human vs. murine models using sequence alignment (e.g., 89% homology in catalytic domain)

Case Example

StudyAntibody CloneLocalizationProposed Resolution
A6G3NuclearEpitope masking in cytoplasm
B4H11CytoplasmicPhosphorylation-dependent epitope

How to design a COBL6 functional blocking assay?

  • Stepwise approach:

    • Binding kinetics: Measure KD via SPR (aim for ≤10 nM affinity)

    • In vitro neutralization: Co-culture COBL6+ cells with antibody (0.1–10 μg/mL), monitor downstream targets (e.g., pERK reduction ≥50%)

    • In vivo validation: Use humanized mouse model with tumor xenografts; measure metastasis inhibition (p<0.05 vs. IgG control)

What strategies improve COBL6 antibody stability in longitudinal studies?

  • Formulation:

    • Add 0.05% sodium azide + 1% trehalose

    • Avoid >3 freeze-thaw cycles; aliquot in single-use volumes

  • Accelerated stability testing:

    ConditionAcceptable Threshold
    37°C, 7 days≤15% aggregation (SEC-HPLC)
    pH 5.0–8.0Retain ≥90% binding (ELISA)

Methodological Notes

  • For epitope binning, use BLI-based cross-blocking assays with ≥5 overlapping mAbs

  • In multiplex assays, confirm lack of cross-reactivity with LY6G6D/CD3 bispecific antibodies

  • Always include Fc receptor blocking steps when working with IgG1 isotypes

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