tbh-1 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
tbh-1 antibody; H13N06.6 antibody; Tyramine beta-hydroxylase antibody; EC 1.14.17.- antibody
Target Names
tbh-1
Uniprot No.

Target Background

Function
TBH-1 antibody is essential for the conversion of tyramine to octopamine, a precursor of octopamine and potentially a neurotransmitter itself. It plays a role in regulating egg laying, which is inhibited by tyramine. Due to its involvement in octopamine biosynthesis, TBH-1 antibody is also required for crtc-1-dependent regulation of AMPK-mediated longevity.
Database Links

STRING: 6239.H13N06.6b

UniGene: Cel.39079

Protein Families
Copper type II ascorbate-dependent monooxygenase family
Subcellular Location
[Isoform b]: Membrane; Single-pass membrane protein.
Tissue Specificity
Present in synaptic regions of RIC interneurons. Present in gonadal sheath cells of hermaphrodites (at protein level).

Q&A

Here’s a structured collection of FAQs for researchers working with tbh-1 Antibody, organized by complexity and grounded in experimental methodology:

What experimental designs are optimal for studying tbh-1 in neurotransmitter regulation?

Advanced Considerations:

  • Stress Assays: Expose tbh-1 mutants to ethanol or heat stress and quantify locomotion defects (e.g., larval crawling assays) .

  • Neuron-Specific Rescue: Use tissue-specific promoters (e.g., nM18-Tbh-Gal4 in Drosophila) to restore tbh-1 in Hugin neurons and assess ethanol tolerance recovery .

  • Isoform-Specific Analysis: Design isoform-specific primers/probes to distinguish splice variants in RT-qPCR .

Table 2: Example Experimental Conditions for Stress Assays

ConditionModel SystemReadoutKey Finding
Ethanol exposureDrosophila adultsLocomotion recovery timeTbh nM18 mutants show 50% reduced tolerance
Heat shockC. elegansOocyte expulsion rateNo defect in tbh-1 mutants

How to resolve contradictions in tbh-1 localization data across studies?

Data Conflict Analysis:

  • Species-Specific Expression: Drosophila Tbh localizes to Hugin neurons and noradrenergic cells, while C. elegans TBH-1 is restricted to head interneurons .

  • Antibody Cross-Reactivity: Validate antibody epitopes using recombinant proteins (e.g., compare Drosophila Tbh vs. C. elegans TBH-1 sequence alignment) .

  • Technical Variability: Optimize fixation protocols (e.g., paraformaldehyde concentration) to preserve epitopes in immunohistochemistry .

What advanced applications support tbh-1 functional studies?

Emerging Techniques:

  • Multiplexed Imaging: Combine tbh-1 antibody with calcium indicators (e.g., GCaMP) to link enzyme expression to neuronal activity.

  • CRISPR-Cas9 Epitope Tagging: Knock in HA/FLAG tags into endogenous tbh-1 loci for orthogonal validation .

  • Single-Cell RNA Sequencing: Profile tbh-1 expression across neuronal subtypes in Drosophila or C. elegans .

How to design epistasis experiments for tbh-1 genetic interactions?

Methodology:

  • Double Mutant Analysis: Cross tbh-1 mutants with strains lacking tyramine (e.g., tdc-1 mutants in C. elegans) to dissect octopamine-independent pathways .

  • Pharmacological Inhibition: Treat with yohimbine (α2-adrenergic antagonist) to isolate Tbh-1’s role in noradrenergic signaling .

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