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- Tel: 858.663.9055
- Email: info@nsjbio.com
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Forkhead box C1, also known asFOXC1, is aproteinwhich in humans is encoded by theFOXC1gene. It is mapped to 6p25.3. This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.
Optimal dilution of the FOXC1 antibody should be determined by the researcher.
A human recombinant protein (amino acids T392-F554) was used as the immunogen for the FOXC1 antibody.
After reconstitution, the FOXC1 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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