FOXC1 FISH Probe
The FOXC1 FISH probe is designed to hybridize to the FOXC1 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
---|---|---|---|---|
FOXC1-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
FOXC1-20-RE | 20 (40 μL) | 200 μL | ||
FOXC1-20-GO | 20 (40 μL) | 200 μL | ||
FOXC1-20-GR | 20 (40 μL) | 200 μL | ||
FOXC1-20-AQ | 20 (40 μL) | 200 μL | ||
FOXC1-20-DIG | 20 (40 μL) | 200 μL | ||
FOXC1-20-BIO | 20 (40 μL) | 200 μL |
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 |
---|
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