BT5 Antibody

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Description

Several validated antibodies target integrin beta 5 (ITGB5), a transmembrane receptor subunit:

ProductCloneApplicationsReactivityKey Data
ab184312EPR19170WBHuman, Mouse, Rat90 kDa observed vs 88 kDa predicted
MAB2528P5H9ICC/IF, NeutralizationHuman-specificBlocks αVβ5-vitronectin interaction
#3629D24A5WB, IP, IFCross-reactive (H,M,R,Mk)90 kDa detection

These antibodies show distinct applications:

  • Cancer research: Detected in HT1080 fibrosarcoma lines

  • Immunofluorescence: 5% NFDM/TBST blocking buffer optimized

  • Species specificity: MAB2528 uniquely detects αVβ5 heterodimer

Drosophila Projectin Antibody (Unlikely Association)

A specialized antibody targeting Drosophila projectin (gene symbol bt) exists as clone P5-3B3 :

CharacteristicSpecification
Host SpeciesMouse
IsotypeIgG1
ApplicationsIF, IHC, WB
Antigen MW743.5 kDa
HybridomaNS-1 myeloma

While scientifically valid, this antibody has no established connection to human therapeutic applications.

Research Gaps and Recommendations

  1. Nomenclature Clarification: No "BT5 Antibody" exists in major repositories (cAb-Rep, OAS). Potential typographical errors require verification.

  2. Therapeutic Candidates: BTLA inhibitors (TAB004) and integrin β5 blockers represent active research fronts with clinical relevance.

  3. Technical Considerations:

    • For BTLA studies: Use 1:1000 dilution in 5% NFDM/TBST buffer

    • For αVβ5 detection: 10 µg/mL concentration optimal for ICC

Researchers should confirm target specificity through:

  • Epitope mapping: Essential given BTLA's structural complexity

  • Cross-validation: Compare with public repertoires (cAb-Rep, OAS)

Emerging Directions in Antibody Engineering

While not directly related to "BT5", adjacent innovations demonstrate field progress:

TechnologyApplicationRelevance
Bispecific Antibodies HIV-1 neutralization94-97% strain coverage via CrossMab format
Octet® BLI Platform Affinity measurementEnables fluidics-free bsAb characterization
Fab-arm Exchange bsAb productionAchieves 98% purity via CH3 domain engineering

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
BT5 antibody; At4g37610 antibody; F19F18.100BTB/POZ and TAZ domain-containing protein 5 antibody; BTB and TAZ domain protein 5 antibody
Target Names
BT5
Uniprot No.

Target Background

Function
BT5 Antibody may function as a substrate-specific adapter within a Cullin 3-RING Box 1-BTB (CUL3-RBX1-BTB) E3 ubiquitin ligase complex. This complex mediates the ubiquitination and subsequent proteasomal degradation of target proteins.
Database Links

KEGG: ath:AT4G37610

STRING: 3702.AT4G37610.1

UniGene: At.28153

Subcellular Location
Cytoplasm.
Tissue Specificity
Preferentially expressed in young leaves, roots and stems.

Q&A

Basic Research Questions

How does BT5 antibody function in bispecific therapeutic applications?

BT5 antibodies operate through dual-targeting mechanisms, binding to conserved viral epitopes (e.g., Spike N-terminal domain) and receptor-binding domains (RBDs) to neutralize SARS-CoV-2 variants . Methodologically:

  • Experimental design: Use surface plasmon resonance (SPR) or cryo-EM to validate binding kinetics and structural interactions .

  • Validation: Confirm neutralization efficacy via pseudovirus assays and in vivo models (e.g., murine lung viral load reduction assays) .

What are critical considerations for validating BT5 antibodies in Western blotting?

  • Specificity: Include positive/negative tissue controls and purified protein standards to confirm target detection .

  • Affinity testing: Optimize dilutions (e.g., 1:500–1:2000) in blocking buffers (5% BSA/TBST) .

  • Reproducibility: Validate across multiple batches using RRIDs to track antibody performance .

How to optimize BT5 antibody use in flow cytometry for cell population analysis?

  • Surface vs. intracellular staining: Permeabilize cells for intracellular targets; use in vivo grade antibodies for live-cell surface markers .

  • Fluorophore selection: Pair with low-autofluorescence conjugates (e.g., PE/Cy7) to minimize background .

Advanced Research Questions

How to resolve contradictions in BT5 antibody performance across experimental platforms?

Contradiction SourceResolution Strategy
Variability in ELISA vs. Western blotRe-evaluate epitope accessibility (native vs. denatured conditions) .
Inconsistent in vivo efficacyAssess pharmacokinetics (e.g., half-life, tissue penetration) and dosage thresholds .
Cross-reactivity in multiplex assaysPerform competitive binding assays with truncated antigens .

What structural insights guide BT5 antibody engineering for broader coronavirus neutralization?

  • NTD-RBD cooperativity: Cryo-EM structures reveal how BT5’s bispecific design stabilizes Spike protein conformations, enabling pan-coronavirus inhibition .

  • CDR loop engineering: Use AI tools like ABodyBuilder2 or IgFold to predict HCDR3 loop conformations for epitope optimization .

How can AI accelerate BT5 antibody development against evolving viral variants?

  • Paratope prediction: Apply Antibody Language Models (ALMs) like AntiBERTy to forecast escape mutations .

  • Multispecies validation: Train models on structural databases (e.g., SAbDab) to predict cross-reactivity with zoonotic coronaviruses .

Methodological Best Practices

  • Data contradiction analysis: Use Boolean minimization (α=2, β=1, θ=1) to identify irreproducible dependencies in antibody performance data .

  • Structural validation: Combine X-ray crystallography (resolution ≤2.5 Å) with molecular dynamics simulations to confirm epitope-paratope interactions .

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