Introduction
The Short Stature Homeobox 2 (SHOX2) gene encodes a transcription factor critical for skeletal development, cardiac function, and neuronal differentiation. Mutations or altered expression of SHOX2 have been linked to congenital disorders, cardiac arrhythmias, and cancer progression (National Center for Biotechnology Information). The SHOX2 Polyclonal Antibody is an essential tool in biomedical research, particularly in the study of growth disorders, cardiovascular diseases, and oncology.
Biological Role of SHOX2
SHOX2 plays a pivotal role in limb formation and craniofacial development (National Institute of Child Health and Human Development). Unlike its homolog SHOX, which is associated with short stature syndromes, SHOX2 has been implicated in atrioventricular conduction and cardiac pacemaker function, making it a subject of interest in cardiac electrophysiology research (National Heart, Lung, and Blood Institute).
Elevated SHOX2 expression has been detected in lung cancer, colorectal cancer, and head and neck squamous cell carcinoma, suggesting its potential as a diagnostic and prognostic marker in oncology (National Cancer Institute).
Applications of SHOX2 Polyclonal Antibody in Research
- Cancer Biomarker Research: SHOX2 is a recognized methylation marker for lung cancer detection in circulating tumor DNA (ctDNA) and biopsy samples (National Library of Medicine).
- Cardiac Development and Disease: Studies indicate that SHOX2 is critical for pacemaker cell development, influencing conduction in the sinoatrial node (American Heart Association). Researchers utilize SHOX2 polyclonal antibodies to map expression in fetal and adult cardiac tissues (NIH).
- Skeletal Growth and Limb Formation: SHOX2 is required for bone elongation, and its disruption is associated with growth retardation disorders such as Langer mesomelic dysplasia (U.S. Department of Health & Human Services).
- Neuronal Differentiation Studies: SHOX2 expression has been linked to neurodevelopment, playing a role in motor neuron identity specification (National Institute of Neurological Disorders and Stroke).
- Epigenetic and Gene Regulation Research: Scientists use SHOX2 polyclonal antibodies to investigate its regulation via DNA methylation and transcription factor interactions (PubMed).
Antibody Characteristics
The SHOX2 Polyclonal Antibody is designed to target SHOX2 protein and is typically raised in rabbit or goat hosts. This antibody is ideal for:
- Western blot analysis to detect SHOX2 expression in various tissues (Centers for Disease Control and Prevention).
- Immunohistochemistry (IHC) and immunofluorescence for cellular localization studies (National Cancer Institute).
- Chromatin immunoprecipitation (ChIP) to study SHOX2-mediated gene regulation (National Human Genome Research Institute).
Considerations for Experimental Use
- Tissue-Specific Expression: SHOX2 is highly expressed in the heart, nervous system, and bones, making sample selection crucial for research (U.S. National Library of Medicine).
- Antibody Dilution Optimization: For IHC, antibody dilution must be optimized to prevent non-specific binding (National Institute of General Medical Sciences).
- Validation in Disease Models: SHOX2 antibodies should be tested in disease models such as congenital heart defects and cancer tissues (National Institute on Deafness and Other Communication Disorders).
Conclusion
The SHOX2 Polyclonal Antibody is a crucial tool for studying developmental biology, cardiology, and oncology. Ongoing research supported by institutions like the National Cancer Institute and NIH continues to explore SHOX2’s role in cancer diagnostics, congenital disorders, and cardiac conduction. Researchers can leverage this antibody to advance biomedical research, particularly in epigenetics, disease progression, and regenerative medicine (National Institutes of Health).
For further reading, refer to peer-reviewed publications available on PubMed and government research institutions such as NIH, NCBI, and the CDC for the latest findings on SHOX2-related research (PubMed).
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