購物車
幫助
021-54845833/15800441009
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Background: |
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. |
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Applications: |
ELISA, WB |
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Name of antibody: |
FOXC1 |
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Immunogen: |
Synthetic peptide of human FOXC1 |
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Full name: |
forkhead box C1 |
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Synonyms： |
ARA; IGDA; IHG1; FKHL7; IRID1; RIEG3; FREAC3; FREAC-3 |
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SwissProt: |
Q12948 |
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ELISA Recommended dilution: |
2000-5000 |
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WB Predicted band size: |
57 kDa |
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WB Positive control: |
Human normal liver tissue |
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WB Recommended dilution: |
500-2000 |
