FOXC1 Break Apart FISH Probe
Empire Genomics’ FOXC1 Break Apart FISH Probe is designed to flank the FOXC1 gene and is typically used for detecting FOXC1 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| FOXC1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-GORE | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-GROR | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-REGO | 20 (40 μL) | 200 μL |
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| FOXC1BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
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. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: FOXC1
Gene Name: Forkhead Box C1
Chromosome: CHR6: 1610680-1614129
Locus: 6p25.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FOXC1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FOXC1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping