HKR1-FECH Fusion FISH Probe
The HKR1-FECH Fusion FISH Probe is used to confirm a fusion of the HKR1 and FECH genes. The fusion of the HKR1 and FECH genes has been associated with Prostate Adenocarcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** 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 |
|---|---|---|---|---|
| HKR1-FECH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-RERE | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-REOR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-REGO | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-REGR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-OROR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GORE | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GROR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| HKR1-FECH-20-AQAQ | 20 (40 μL) | 200 μL |
|
FECH Gene Summary
The protein encoded by this gene is localized to the mitochondrion, where it catalyzes the insertion of the ferrous form of iron into protoporphyrin IX in the heme synthesis pathway. Mutations in this gene are associated with erythropoietic protoporphyria. Two transcript variants encoding different isoforms have been found for this gene. A pseudogene of this gene is found on chromosome 3.[provided by RefSeq, May 2010]
Gene Name: Ferrochelatase
Chromosome: CHR18: 55212072 -55253969
Locus: 18q21.31
HKR1 Gene Summary
The HKR1, GLI-Kruppel Zinc Finger Family Member (HKR1) gene is located on chr19 :37825579-37855357 at 19q13.12.
Gene Name: HKR1, GLI-Kruppel Zinc Finger Family Member
Chromosome: CHR19: 37825579 -37855357
Locus: 19q13.12
Gene Diseases
The HKR1 FECH Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|