sox-2 Antibody

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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
sox-2 antibody; K08A8.2 antibody; Transcription factor sox-2 antibody
Target Names
sox-2
Uniprot No.

Target Background

Function
SOX-2 is a transcription factor that plays a crucial role in regulating the lineage progression of embryonic blast cells and controlling the postmitotic specification and differentiation of neurons. It collaborates with other factors to direct the differentiation of olfactory neurons, functioning alongside the transcription factor CEH-36 to specify AWC neurons and with the LIM homeodomain factor LIM-4 to suppress AWC terminal differentiation and promote AWB neuron differentiation. SOX-2 also participates in the terminal differentiation of glutamatergic and cholinergic neurons. Furthermore, it is essential for natural reprogramming events, particularly for the transdifferentiation of the Y rectal epithelial cell to the PDA motor neuron during larval development.
Gene References Into Functions
  1. The role of SOX2 in neurogenesis and stem cell differentiation has been extensively studied. PMID: 26743825
  2. SOX-2 interacts with different transcription factors to diversify postmitotic olfactory cell types. PMID: 26341465
  3. Genetic analyses have revealed the requirement of components of the NODE complex, recently identified in embryonic stem (ES) cells, and of the OCT4 partner SOX-2, for the initiation of this natural direct reprogramming event. PMID: 22493276
Database Links

KEGG: cel:CELE_K08A8.2

STRING: 6239.K08A8.2a.1

UniGene: Cel.17061

Subcellular Location
Nucleus.
Tissue Specificity
Expressed in AWC and AWB olfactory neurons throughout life. Also expressed in the IL1, IL2, URA, URB and OLL sensory neurons, the AIM, AIN, AVK, RIH interneurons, and the motor neuron class RME.

Customer Reviews

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Applications : WB

Sample type: Human X02 brain cancer stem cells

Review: The expression levels of stem cell markers such as Nestin, SOX-2 and CXCR4 in X02 cells, U373, U87 and T98G by Western blotting. β-actin was used as loading control.

Q&A

FAQs for SOX2 Antibody Research

Advanced Research Questions

How to resolve contradictions in SOX2 antibody associations with paraneoplastic syndromes?

  • Data conflict:

    • Study found no SOX2/HuD antibody co-occurrence in SCLC patients with neurologic symptoms, while reported SOX2 antibodies in 61% of LEMS-SCLC cases.

    • Resolution strategy:

      • Stratify cohorts by neurologic symptom severity and tumor subtype.

      • Use orthogonal methods (ELISA + Western blot) to confirm antibody specificity .

      • Analyze SOX2 isoform expression differences across SCLC subtypes .

What methodologies optimize detection of SOX2 autoantibodies in serum?

  • Technical workflow:

    • Dilution series ELISA: Test sera at 1:110 to 1:6400 dilutions to capture low-titer responses .

    • Dose-response validation: Require ≥1.6 nM antigen binding and OD > mean + 3 SD of controls .

    • Cross-validation: Pair phage display assays (for epitope mapping) with Western blotting to reduce false positives .

How do SOX2-protein interactions influence epigenetic regulation in cancer?

  • Mechanistic insights:

    • HDAC1/2 binding: Sox2’s HMG domain facilitates interaction with HDAC2, but deletion of this domain increases HDAC1 association, suggesting competitive binding dynamics .

    • Experimental approach:

      • Co-immunoprecipitation (Co-IP) with domain-specific Sox2 mutants (e.g., ΔHMG) .

      • Chromatin immunoprecipitation (ChIP) to map SOX2/HDAC co-localization sites .

What statistical considerations are critical for SOX2 antibody cohort studies?

  • Design principles:

    • Power analysis: For SCLC vs. control comparisons, a minimum cohort of 75 patients/group achieves 80% power (α=0.05) given 35% vs. 6% positivity .

    • Confounding factors: Adjust for smoking status (SCLC bias) and autoimmune comorbidities in multivariate models .

Can SOX2 serve as a target for T-cell-based immunotherapy?

  • Preclinical evidence:

    • HLA-A*0201-restricted SOX2 peptides (e.g., TLMKKDKYTL) elicit glioma-reactive CD8+ T-cells in vitro .

    • Challenge: SOX2’s role in normal neural stem cells necessitates tumor-specific delivery to avoid off-target effects .

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