CEP192-AFG3L2 Fusion FISH Probe
The CEP192-AFG3L2 Fusion FISH Probe is used to confirm a fusion of the CEP192 and AFG3L2 genes. The fusion of the CEP192 and AFG3L2 genes has been associated with Lung Squamous Cell Carcinoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CEP192-AFG3L2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| CEP192-AFG3L2-20-AQAQ | 20 (40 μL) | 200 μL |
|
AFG3L2 Gene Summary
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]
Gene Name: AFG3 Like Matrix AAA Peptidase Subunit 2
Chromosome: CHR18: 12328942 -12377275
Locus: 18p11.21
CEP192 Gene Summary
The Centrosomal Protein 192 (CEP192) gene is located on chr18 :12991360-13125051 at 18p11.21.
Gene Name: Centrosomal Protein 192
Chromosome: CHR18: 12991360 -13125051
Locus: 18p11.21
Gene Diseases
The CEP192 AFG3L2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|