PGL5 Antibody

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Description

Clarification of Terminology

  • PGL-I vs. PGL5:
    Multiple sources reference PGL-I (phenolic glycolipid I), a Mycobacterium leprae-specific antigen used in leprosy diagnostics . This is unrelated to "PGL5," which is not described in leprosy research.

    • Key function: PGL-I antibodies correlate with multibacillary leprosy and bacilloscopic index .

    • Diagnostic platforms: Phage display-derived PGL-I mimotopes and scFv antibodies show promise for ELISA and SPR-based immunosensors .

  • LGR5/GPR49 Antibodies:
    Extensive data exists for antibodies targeting LGR5 (leucine-rich repeat-containing G-protein coupled receptor 5), a colorectal cancer biomarker . These include:

    • Mouse monoclonal antibodies (e.g., MAB8240) validated in flow cytometry and immunocytochemistry .

    • Human/mouse cross-reactive antibodies (e.g., MAB8078) with cytoplasmic and surface staining specificity .

    • Therapeutic applications: Antibody-drug conjugates (ADCs) and magnetoliposomes targeting LGR5+ cancer stem cells .

  • PGL5 Enzyme:
    UniProt identifies PGL5 (Q8LEV7) as a probable 6-phosphogluconolactonase involved in carbohydrate metabolism . No antibodies against this enzyme are documented in the provided sources.

Table 1: Disambiguation of Relevant Terms

TermDefinitionAntibody StatusKey Sources
PGL-IMycobacterium leprae phenolic glycolipidWell-characterized (diagnostic use)
LGR5/GPR49Stem cell marker in colorectal cancerValidated (therapeutic/diagnostic use)[3-6]
PGL5 (Q8LEV7)Metabolic enzyme: 6-phosphogluconolactonaseNo antibodies reported

Key Observations:

  1. Nomenclature Conflict: "PGL5" is either a typographical error (e.g., intended as PGL-I or LGR5) or refers to the uncharacterized enzyme Q8LEV7.

  2. Absence of Experimental Data: No studies describe the development, validation, or application of antibodies against PGL5 (6-phosphogluconolactonase).

Hypothetical Context for PGL5 Antibody Development

If targeting the PGL5 enzyme (Q8LEV7), antibody generation would require:

  • Immunogen Design: Recombinant PGL5 protein or peptide epitopes.

  • Validation Assays:

    • Functional tests: Inhibition of 6-phosphogluconolactone hydrolysis .

    • Localization: Subcellular staining in metabolic tissues (e.g., liver).

  • Therapeutic Potential: Unclear, as PGL5’s role in disease is not established.

Recommendations for Further Research

  1. Clarify Target Identity: Confirm whether "PGL5" refers to LGR5, PGL-I, or the metabolic enzyme.

  2. Explore Related Systems:

    • LGR5-targeted therapies show efficacy in colorectal cancer models .

    • PGL-I antibodies remain critical for leprosy diagnosis .

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
14-16 week lead time (made-to-order)
Synonyms
PGL5 antibody; At5g24420 antibody; K16H17.13Probable 6-phosphogluconolactonase 5 antibody; 6PGL5 antibody; EC 3.1.1.31 antibody
Target Names
PGL5
Uniprot No.

Target Background

Function
This antibody targets 6-phosphogluconolactone phosphatase, an enzyme that catalyzes the hydrolysis of 6-phosphogluconolactone to 6-phosphogluconate.
Database Links

KEGG: ath:AT5G24420

STRING: 3702.AT5G24420.1

UniGene: At.8628

Protein Families
Glucosamine/galactosamine-6-phosphate isomerase family, 6-phosphogluconolactonase subfamily
Subcellular Location
Cytoplasm, cytosol.

Q&A

Here’s a structured FAQ for researchers investigating antibodies targeting LGR5 (GPR49) and PGL-related epitopes, synthesized from peer-reviewed studies:

How do I validate the specificity of anti-LGR5 antibodies in murine intestinal stem cell models?

Methodological Answer:

  • Use dual-reporter systems (e.g., Lgr5-GFP/Bmi1-GFP mice) combined with flow cytometry and immunofluorescence to confirm antibody colocalization with stem cell markers .

  • Validate via competitive blocking assays with recombinant LGR5 extracellular domain (Lys375-Pro547) .

  • Perform qRT-PCR on sorted cells to correlate antibody-positive populations with Lgr5 mRNA levels .

What are key applications of anti-PGL antibodies in developmental biology?

Methodological Answer:

  • PGL-1/PGL-3 detection: Use KT3 monoclonal antibody for immunostaining of C. elegans P granules. Validate specificity via RNAi knockdown of pgl-1/pgl-3 and western blotting of peptide fragments .

  • Functional studies: Combine with GFP-tagged transgenes to track granule dynamics during embryogenesis .

How can I distinguish between LGR5+ cancer stem cells and normal epithelial cells?

Methodological Answer:

  • Apply antibody-functionalized magnetoliposomes (e.g., anti-LGR5 MAB8240) for magnetic-activated cell sorting (MACS) .

  • Use TOPflash luciferase assays to confirm Wnt pathway activation in sorted cells .

How do I resolve contradictory data on LGR5 antibody performance across cell lines?

Methodological Answer:

FactorSolution
Epitope accessibilityCompare fixed vs. live-cell staining; use antigen retrieval for formalin-fixed samples .
Cell line variabilityValidate LGR5 expression via CRISPR knockout controls (e.g., MC38-L(-) cells) .
Batch variabilityInclude isotype controls and standardize antibody dilutions across experiments .

What strategies improve LGR5-targeted drug delivery in colorectal cancer models?

Methodological Answer:

  • Functionalize oxaliplatin-loaded magnetoliposomes with anti-LGR5 antibodies (e.g., MCLA-158) for receptor-mediated uptake. Assess efficacy via:

    • Proliferation assays: IC50 reduced 3.2-fold vs. free drug .

    • Hyperthermia: Apply alternating magnetic fields (AMF) for localized drug release .

  • Validate tumor specificity using MC38-L(-) controls to confirm LGR5 dependency .

How can I design multiplex assays to study LGR5/PGL interactions in vivo?

Methodological Answer:

  • Combine anti-LGR5 immunoPET tracers (e.g., ⁸⁹Zr-DFO-8F2) with fluorescent KT3 antibody staining for dual-modality imaging .

  • Use surface plasmon resonance (SPR) to quantify binding kinetics between LGR5 antibodies and R-spondin ligands .

Data Contradiction Analysis

Example: Discrepancies in LGR5 antibody staining between intestinal crypts and tumor xenografts .

  • Root cause: Tumor microenvironment alters LGR5 glycosylation, masking epitopes.

  • Solution: Treat samples with PNGase F to remove N-linked glycans before staining .

Key Findings from Literature

AntibodyTargetApplicationCritical Insight
KT3 PGL-1/PGL-3Developmental biologyBinds intrinsically disordered regions (IDRs); cross-reactivity requires RNAi validation.
MAB8240 LGR5Cancer therapyInduces Wnt signaling in HEK293 cells; efficacy enhanced by R-spondin coadministration.
8F2/9G5 LGR5ImmunoPETHigher tumor-to-background ratio in PDX models than clinical biopsies.

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