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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
MFSD4A antibody detects Major facilitator superfamily domain-containing protein 4A, a predicted membrane transporter encoded by the MFSD4A gene located on chromosome 1p33. MFSD4A is a member of the major facilitator superfamily (MFS), one of the largest groups of secondary transporters responsible for moving small solutes across biological membranes. The MFSD4A protein localizes to the plasma membrane and intracellular vesicles, where it is believed to participate in nutrient sensing and metabolite transport. Although its substrate specificity is still under investigation, MFSD4A shares structural features with sugar and amino acid transporters, suggesting a role in metabolic regulation and intercellular signaling.
MFSD4A antibody identifies a multi-pass transmembrane protein that contains 12 predicted alpha-helical transmembrane domains arranged in a canonical MFS fold. This structure allows alternating access transport of solutes driven by proton or sodium gradients. The cytoplasmic loops and termini of MFSD4A may interact with signaling molecules that modulate transporter activity in response to nutrient status or hormonal cues. Expression profiling reveals that MFSD4A is enriched in liver, pancreas, and brain tissues, consistent with its proposed role in metabolic homeostasis and neuronal energy regulation.
Functionally, MFSD4A may participate in glucose or amino acid transport pathways and contribute to the regulation of insulin secretion and energy metabolism. Emerging transcriptomic data indicate that MFSD4A expression is responsive to fasting, insulin signaling, and circadian rhythm regulators. In neurons, it may be involved in neurotransmitter or metabolite shuttling across synaptic membranes. Given its homology with nutrient transporters, MFSD4A is under study as a potential metabolic sensor that links energy availability to intracellular signaling pathways such as mTOR and AMPK.
From a structural and evolutionary perspective, MFSD4A belongs to the major facilitator superfamily, which includes transporters for sugars, ions, and small molecules. Members of this family typically share conserved sequence motifs such as the MFS signature (GXXXDRXGRR) involved in proton coupling and conformational switching. These features support the hypothesis that MFSD4A mediates solute exchange across cell membranes. Its expression in metabolically active tissues suggests integration with pathways governing glucose utilization and lipid metabolism.
Dysregulation of MFSD4A has been observed in metabolic disorders and certain cancers. Genome analyses have identified associations between MFSD4A variants and altered plasma metabolite levels, insulin resistance, and hepatocellular carcinoma progression. In the nervous system, perturbations in MFSD4A expression may influence neuronal excitability and cognitive function through metabolic imbalance. The protein's role in membrane transport and nutrient sensing positions it as a potential target for metabolic and neurological research.
Immunohistochemical staining using MFSD4A antibody reveals membrane localization in hepatocytes, pancreatic islets, and neurons. MFSD4A antibody from NSJ Bioreagents is an important reagent for studying membrane transport, metabolic regulation, and nutrient signaling mechanisms at the cellular level.
Optimal dilution of the MFSD4A antibody should be determined by the researcher.
E.coli-derived human MFSD4A recombinant protein (Position: S48-R514) was used as the immunogen for the MFSD4A antibody.
After reconstitution, the MFSD4A antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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