TBL8 Antibody

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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
TBL8 antibody; At3g11570 antibody; Q9CAX1 antibody; Protein trichome birefringence-like 8 antibody
Target Names
TBL8
Uniprot No.

Target Background

Function
TBL8 Antibody may function as a bridging protein, linking pectin and other cell wall polysaccharides. It likely plays a role in maintaining pectin esterification. Additionally, it may be involved in the specific O-acetylation of cell wall polymers.
Database Links

KEGG: ath:AT3G11570

STRING: 3702.AT3G11570.1

UniGene: At.28347

Protein Families
PC-esterase family, TBL subfamily
Subcellular Location
Membrane; Single-pass type II membrane protein.

Q&A

FAQs for Researchers on TRPM8 Antibody Applications in Academic Research
Note: Based on review of peer-reviewed studies, including validation data from and computational design frameworks from . TBL8 antibody references were not identified in indexed literature; responses focus on TRPM8 due to contextual relevance.

Advanced Research Questions

  • How to reconcile contradictory data from TRPM8 antibodies across WB, ICC, and IHC?

    AntibodyWB PerformanceICC SR (1:200)IHC Reliability
    ECM1High4.2Moderate
    Origene1Moderate3.8High
    AlomoneVariable2.1Low
    Data adapted from
    • Root cause analysis: Optimize antibody dilutions (e.g., ECM1 performs better at 1:500 vs. 1:200).

    • Cross-validation: Pair antibody-based results with functional assays (e.g., calcium imaging in TRPM8+ cells) .

  • What computational strategies improve antibody design for TRPM8 studies?

    • CDR grafting: Use tools like RosettaAntibodyDesign (RAbD) to sample canonical CDR clusters and optimize interface energy (ΔG ≤ −15 Rosetta Energy Units recommended) .

    • Risk mitigation: Calculate design risk ratio (DRR) to prioritize native-like conformations (DRR > 1.0 indicates successful recovery of native clusters) .

Methodological Recommendations

  • How to optimize TRPM8 detection in low-abundance native tissues?

    • Signal amplification: Combine tyramide-based systems with high-SR antibodies (e.g., Origene1).

    • Multiplex validation: Correlate antibody signals with RNAscope™ probes for Trpm8 mRNA .

  • What statistical approaches resolve conflicting antibody performance metrics?

    • Cluster analysis: Group antibodies by SR values and technical reproducibility (CV ≤ 20% for ICC).

    • Bayesian inference: Model likelihood of true-positive detection using prior validation data from overexpression systems .

Key Validation Criteria from

  • Western blot: Require clear bands at ~128 kDa (TRPM8 monomer) without cross-reactivity.

  • Functional correlation: Antibody performance should align with TRPM8-dependent phenotypes (e.g., menthol-induced calcium flux).

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