daf-37 Antibody

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Product Specs

Buffer
Preservative: 0.03% ProClin 300
Components: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
14-16 Week Lead Time (Made-to-Order)
Synonyms
daf-37 antibody; C30B5.5G-protein coupled receptor daf-37 antibody; Abnormal dauer formation protein 37 antibody
Target Names
daf-37
Uniprot No.

Target Background

Function
The daf-37 antibody targets a G-protein coupled receptor (GPCR) that forms a heterodimer with daf-38, regulating dauer formation and behavior. It serves as a receptor for the ascaroside pheromone ascr#2 and is essential for responding to dauer-inducing pheromones, particularly ascr#2. daf-37 exhibits neuron-specific functions in response to ascr#2. In ASI neurons, it controls dauer formation in larvae, while in ASK neurons, it influences longevity and hermaphrodite repulsion. It is believed to function upstream of the daf-11, daf-7, and daf-2 signaling pathways.
Database Links
Protein Families
G-protein coupled receptor 1 family
Subcellular Location
Cell membrane; Multi-pass membrane protein. Cell projection, cilium. Golgi apparatus.
Tissue Specificity
Expressed in the ASI and ASK chemosensory neurons, in the IL-2 interneurons, and in the male specific CEM (cephalic sensilla, male) neurons.

Q&A

Based on the provided search results and analysis of available scientific literature, here is a structured FAQ collection addressing key research considerations for antibody-related studies in immunosenescence and receptor interaction research:

How to validate antibody specificity for immune senescence biomarkers in aging studies?

  • Perform multiplexed validation using:

    • Flow cytometry for immune cell subset frequencies (e.g., CD4+/CD8+ ratios)

    • Cytokine response profiling via Luminex arrays (IL-6, TNF-α, IFN-γ)

    • Competitive inhibition assays with recombinant DAF SCR domains

  • Critical controls:

    • Isotype-matched negative controls

    • Knockout cell lines for target biomarkers

What methodological considerations apply to antibody-based detection of complement regulatory proteins?

ParameterDAF (CD55) AnalysisTechnical Considerations
EpitopeSCR domains 2-4 Confirm domain specificity via truncated protein variants
AssayCryoEM binding studiesLow receptor occupancy requires ≥15% density threshold
Cross-reactivityEchovirus co-receptorsValidate with viral plaque inhibition assays

How to resolve contradictory data in antibody-mediated receptor activation studies?

Case Example: Discrepancies in ErbB2 phosphorylation reports

  • Experimental redesign:

    • Compare antibody clones (e.g., 4D5 vs. MGR3) in isogenic cell lines

    • Use single-molecule localization microscopy to quantify receptor clustering

    • Perform phosphoproteomic time-course analyses (0-60 min post-treatment)

Key Finding:

"DAF SCR2-3 domains show 65% plaque inhibition efficiency compared to SCR1-4 (85%), indicating domain-dependent functional impacts" .

What integrated approaches address low-affinity antibody interactions in structural studies?

  • Combine methodologies:

    • Hydrogen-deuterium exchange mass spectrometry (HX-MS) for epitope mapping

    • Negative-stain EM screening prior to cryoEM (enhances particle selection)

    • Surface plasmon resonance with <i>k</i><sub>off</sub> analysis (10<sup>-3</sup> s<sup>-1</sup> threshold)

How to improve antibody fragments for diagnostic applications?

  • Developability enhancement strategies:

    • Framework mutagenesis (e.g., [28D]-FR1-H mutation reduces aggregation)

    • Multimodal chromatography polishing (HCP reduction to <50 ppm)

    • Camelid VHH engineering for improved thermal stability (ΔT<sub>m</sub> +8°C)

What orthogonal techniques validate antibody-mediated signaling modulation?

TechniqueApplicationKey Metrics
Microscale thermophoresisBinding affinityK<sub>D</sub> ≤ 100 nM
RNA-SeqPathway activation≥2-fold change in NF-κB targets
CrystallographyStructural validation3Å resolution threshold

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