FYCO1 Break Apart FISH Probe
Empire Genomics’ FYCO1 Break Apart FISH Probe is designed to flank the FYCO1 gene and is typically used for detecting FYCO1 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange 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 |
|---|---|---|---|---|
| FYCO1BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-ORGR | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| FYCO1BA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
This gene encodes a protein that contains a RUN domain, FYVE-type zinc finger domain and Golgi dynamics (GOLD) domain. The encoded protein plays a role in microtubule plus end-directed transport of autophagic vesicles through interactions with the small GTPase Rab7, phosphatidylinositol-3-phosphate (PI3P) and the autophagosome marker LC3. Mutations in this gene are a cause of autosomal recessive congenital cataract-2 (CATC2). [provided by RefSeq, Dec 2011]
Gene Details
Gene Symbol: FYCO1
Gene Name: FYVE And Coiled-coil Domain Containing 1
Chromosome: CHR3: 45959394-46037307
Locus: 3p21.31
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: FYCO1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FYCO1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping