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| Size | List Price | Price | Cart |
|---|---|---|---|
| 100 ug | $365.00 | Add to Cart |
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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FOXC1 staining of paraffin embedded Human Kidney (dilution (3µg/ml) . Microwaved antigen retrieval with Tris/EDTA buffer pH9, HRP-staining. Protocol on Data-sheet.
FOXC1 staining of paraffin embedded Human Kidney (dilution (3µg/ml) . Microwaved antigen retrieval with Tris/EDTA buffer pH9, HRP-staining. Protocol on Data-sheet.
FOX1C staining (dilution: 0.5µg/ml)of Human Bone Marrow lysate (RIPA buffer, 35µg total protein per lane). Primary incubated for 1 hour. Detected by western blot using chemiluminescence.
FOX1C staining (dilution: 0.5µg/ml)of Human Bone Marrow lysate (RIPA buffer, 35µg total protein per lane). Primary incubated for 1 hour. Detected by western blot using chemiluminescence.