TOM2B Antibody

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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
TOM2B antibody; TTM1 antibody; At1g32370 antibody; F5D14.14 antibody; Tobamovirus multiplication protein 2B antibody; AtTOM2B antibody
Target Names
TOM2B
Uniprot No.

Target Background

Function
TOM2B Antibody is essential for the efficient intracellular multiplication of tobamoviruses.
Database Links

KEGG: ath:AT1G32370

STRING: 3702.AT1G32370.2

UniGene: At.40151

Q&A

Here’s a structured FAQ for researchers working with TOM2B antibodies, synthesized from academic literature and tailored to experimental design and data interpretation:

Advanced Research Questions

How to resolve contradictory data on TOM2B’s role in viral vs. mitochondrial processes?

  • Context-dependent analysis:

    SystemTOM2B FunctionKey Evidence
    Plant cellsFacilitates viral replicationInteraction with TOM1 helicase promotes viral RNA synthesis
    Mammalian cellsMitochondrial membrane organizationCo-localization with TOMM20 in immunofluorescence

What computational tools predict TOM2B-protein interaction interfaces?

  • Use AlphaFold-Multimer for structural predictions and Rosetta for binding energy calculations, as demonstrated in nanobody design workflows .

  • Validate interfaces via alanine-scanning mutagenesis coupled with IP .

How to design epitope-specific antibodies against TOM2B?

  • Epitope mapping: Combine phage display libraries with deep mutational scanning to identify immunodominant regions .

  • Deimmunization: Use ESM-2 language models to reduce T-cell epitopes while preserving binding affinity .

Key Experimental Parameters for TOM2B Studies

AssayConditionsCritical Controls
Western Blot10 µg lysate, 1:1000 dilutionTOM2B-knockout lysate, β-actin loading control
Co-IP0.5 mg lysate, 50 µl protein G beadsIgG-isotype control, bead-only control
IF/ICC4% PFA fixation, 0.1% Triton permeabilizationSecondary antibody-only control

Addressing Data Conflicts

  • Orthogonal validation: When Western blot bands conflict with predicted sizes (e.g., 70 kDa vs. 16 kDa), perform size-exclusion chromatography to isolate native complexes .

  • Functional rescue: Re-express TOM2B in knockout models to confirm phenotype reversibility .

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