dlat-1 Antibody

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Description

Anti-DLAT Antibodies in Research

Commercial anti-DLAT antibodies are widely used for detecting DLAT in Western blot (WB), immunohistochemistry (IHC), and immunofluorescence (IF). Representative products include:

Product CodeHostApplicationsReactivityKey Features
13426-1-AP RabbitWB, IHC, IF, IPHuman, Mouse, RatValidated in >47 studies; mitochondrial focus
CAB14530 RabbitWB, IHC-P, IF/ICCHuman, Mouse, RatTargets residues 87–270; links to ATP synthesis
23133 MouseWB, ELISAHumanClone 4A4-B6-C10; PDCE2 specificity

Autoimmune and Neurological Disorders

  • Chronic Inflammatory Demyelinating Polyneuropathy (CIDP):

    • Anti-DLAT IgG/IgM antibodies are detected in 18% of CIDP patients, correlating with sensory ataxia (69% vs. 37% in seronegative cases), cranial nerve involvement (24%), and malignancy (20%) .

    • DLAT is highly expressed in dorsal root ganglion cells, suggesting a role in sensory neuropathy pathogenesis .

Cancer Prognosis

  • Gastric Cancer (GC): DLAT upregulation correlates with poor survival, lymph node metastasis, and Th2 immune cell infiltration. It is a potential cuproptosis-related prognostic marker .

Primary Biliary Cirrhosis (PBC):

  • DLAT is the primary antigen for antimitochondrial antibodies (AMA) in 95% of PBC cases, driving bile duct destruction .

Mechanistic Insights

  • Metabolic Regulation: DLAT supports ATP generation via acetyl-CoA production . Dysregulation is linked to diabetes and cancer .

  • Immune-Mediated Damage: Anti-DLAT antibodies may induce T-cell activation against sensory neurons or mitochondrial components .

Research Applications and Validation

  • Key Studies:

    • Neuropathy Biomarker: ELISA and cell-based assays confirm anti-DLAT antibodies in CIDP sera (sensitivity: 18%; specificity: 98.6%) .

    • Mitochondrial Staining: DLAT antibodies localize to mitochondrial matrices in IHC .

Limitations and Future Directions

  • Diagnostic Utility: Cross-reactivity with other mitochondrial antigens requires further validation .

  • Therapeutic Targeting: DLAT’s role in cuproptosis offers avenues for cancer therapy .

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
14-16 weeks lead time (made-to-order)
Synonyms
dlat-1 antibody; F23B12.5 antibody; Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex antibody; mitochondrial antibody; EC 2.3.1.12 antibody; Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex antibody; Pyruvate dehydrogenase complex component E2 antibody; PDC-E2 antibody; PDCE2 antibody
Target Names
dlat-1
Uniprot No.

Target Background

Function
The pyruvate dehydrogenase complex (PDC) catalyzes the conversion of pyruvate to acetyl-CoA and CO2. This multi-enzyme complex comprises multiple copies of three catalytic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2), and lipoamide dehydrogenase (E3).
Database Links
Protein Families
2-oxoacid dehydrogenase family
Subcellular Location
Mitochondrion matrix.

Q&A

Here’s a structured collection of FAQs tailored for academic researchers working with DLAT-1 antibodies, incorporating methodological insights and data from peer-reviewed studies:

How do I validate DLAT-1 antibody specificity in experimental models?

Methodological Answer:

  • Perform Western blot (WB) using cell lysates with known DLAT expression (e.g., HepG2, MCF-7) and include knockout controls .

  • Use immunoprecipitation (IP) followed by mass spectrometry to confirm target binding .

  • Validate cross-reactivity across species (human, mouse, rat) using tissues with confirmed DLAT expression (e.g., liver cancer vs. kidney tissue) .

  • Compare observed molecular weight (~69-70 kDa) against calculated weight (70 kDa) to rule out non-specific bands .

What are optimal dilution ranges for DLAT-1 antibodies in common applications?

Experimental Design Guidelines:

ApplicationDilution RangeKey Validation Data
WB1:2,000–1:10,000HepG2 lysates show clear bands at 70 kDa
IHC1:500–1:2,000Strong staining in human liver cancer tissue with TE buffer antigen retrieval
IF/ICC1:50–1:500Confirmed cytoplasmic localization in HepG2 cells

How does DLAT expression correlate with immune checkpoint markers in hepatocellular carcinoma (HCC)?

Data-Driven Analysis:

What functional pathways are enriched in DLAT-associated gene networks?

Multi-Omics Integration:

  • PPI Network: DLAT interacts with 259 genes (132 positive, 127 negative) .

  • Pathway Enrichment (KEGG):

    PathwayAdjusted p-valueKey Genes
    Metabolic reprogramming< 0.001ACLY, IDH2
    Immune regulation0.003CD274, CTLA4
  • Functional Validation: CRISPR/Cas9 knockout followed by RNA-seq to identify dysregulated metabolic and immune pathways.

How to resolve discrepancies in DLAT-1 antibody performance across studies?

Contradiction Analysis Framework:

FactorPotential IssueResolution Strategy
Clone specificityPolyclonal (13426-1-AP) vs. monoclonal (68303-1-Ig) differences Compare epitope mapping data; validate with orthogonal assays (e.g., ELISA).
Tissue heterogeneityVariable DLAT levels in HCC vs. neuropathies Use disease-specific positive controls (e.g., CIDP sera for neurological studies) .

Can DLAT-1 antibodies serve as biomarkers for non-oncological conditions?

Cross-Disciplinary Evidence:

  • CIDP Diagnosis: Anti-DLAT antibodies are detected in 12% of chronic inflammatory demyelinating polyneuropathy (CIDP) cases, correlating with sensory ataxia (OR = 3.2) .

  • Methodological Note: Screen patient sera via ELISA using recombinant DLAT protein, followed by confirmatory WB .

What are best practices for combining DLAT-1 IHC with PD-1/PD-L1 blockade studies?

Translational Workflow:

  • Preclinical Models: Treat PDX mice with anti-PD-L1 agents (e.g., atezolizumab) and assess DLAT expression via IHC .

  • Data Integration:

    • Correlate DLAT levels with CD8+ T-cell infiltration (flow cytometry).

    • Use spatial transcriptomics to map DLAT/PD-L1 co-expression zones.

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