- Tel: 858.663.9055
- Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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MFN2 is a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system.
Titration of the MFN2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 447-476 from the human protein was used as the immunogen for this MFN2 antibody.
Aliquot the MFN2 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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