UGT92A1 Antibody

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Description

Definition and Functional Role

UGT1A1 antibodies target the UDP-glucuronosyltransferase 1A1 enzyme, responsible for glucuronidating bilirubin, hormones, and drugs like irinotecan . Deficiencies in UGT1A1 activity are linked to Gilbert’s syndrome and increased toxicity risks in chemotherapy .

Pharmacogenomics

  • UGT1A1*28 Polymorphism: A 7-TA repeat variant reduces enzyme activity by 30%, increasing irinotecan toxicity (severe neutropenia: 45% vs. 18% with dose reduction) .

  • Sacituzumab Govitecan: Homozygous UGT1A128 patients had higher treatment discontinuation rates due to adverse effects (25% vs. 10% in heterozygotes) .

Drug Metabolism Studies

  • Cabotegravir Glucuronidation: UGT1A1 metabolizes 67% of this HIV integrase inhibitor, with novel variants (e.g., 454C>A) identified in diverse populations .

Technical Validation Data

  • Western Blot Performance:

    • Proteintech’s antibody detects bands at 50–70 kDa in mouse liver .

    • R&D Systems’ antibody shows a single band at 57 kDa in human liver lysates .

  • Immunohistochemistry: Both antibodies localize UGT1A1 to hepatocytes and intestinal epithelia .

Clinical Implications

ScenarioRisk/Benefit ConsiderationCitation
Irinotecan TherapyUGT1A128 testing reduces severe neutropenia by 60%
Sacituzumab UseHomozygous UGT1A128 increases discontinuation risk 2.5-fold
HIV PreventionUGT1A1 variants alter cabotegravir pharmacokinetics

Limitations and Future Directions

  • Antibody Specificity: Cross-reactivity with other UGT isoforms remains a concern, necessitating knockout validation .

  • Dose Optimization: Prospective trials are needed to confirm whether genotype-guided dosing preserves anticancer efficacy .

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
UGT92A1 antibody; At5g12890 antibody; T24H18.60 antibody; UDP-glycosyltransferase 92A1 antibody; EC 2.4.1.- antibody
Target Names
UGT92A1
Uniprot No.

Q&A

Based on analysis of current research literature and antibody characterization data, here's a structured FAQ addressing critical research considerations for working with UDP-glucuronosyltransferase antibodies:

Advanced Research Challenges

What strategies overcome cross-reactivity in UGT isoform quantification using polyclonal antibodies?

Develop a multiplex immunoaffinity LC-MS workflow:

  • Antibody-based enrichment of target UGT isoform

  • Trypsin digestion with signature peptide selection (e.g., VVMPEVSWQLGR for UGT1A9)

  • Parallel reaction monitoring for isoform-specific quantification

How to design longitudinal studies assessing UGT antibody stability in chronic exposure models?

Incorporate these controls:

  • Antibody performance metrics: Batch-to-batch EC50 variation <15%

  • Matrix effects: Spiked recovery tests in plasma vs tissue homogenates

  • Temporal validation: Monthly re-calibration against NIST reference materials

What computational approaches enhance UGT antibody validation for 3D tissue models?

Implement spatial proteomics integration:

  • Antibody-derived tagging combined with MALDI-IMS for glucuronide distribution mapping

  • Deep learning-based pattern recognition of staining intensity gradients

  • Microfluidic antibody validation chips with 12-plex UGT isoform arrays

Data Interpretation Framework

Contradiction Resolution Protocol
When facing conflicting results from UGT antibody-based assays:

  • Technical Validation

    • Repeat with alternative detection system (chemiluminescence vs fluorescence)

    • Compare monoclonal vs polyclonal antibody performance

  • Biological Contextualization

    • Correlate with mRNA expression (R² ≥0.7 expected in hepatic tissue)

    • Validate against known ontogeny patterns (e.g., UGT1A1 maturation curve)

  • Advanced Correlation

    • Establish pharmacometric models linking protein expression to metabolic clearance

    • Perform systems biology analysis incorporating UGT interactome data

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