SPEF2-C5ORF42 Fusion FISH Probe
The SPEF2-C5ORF42 Fusion FISH Probe is used to confirm a fusion of the SPEF2 and C5ORF42 genes. The fusion of the SPEF2 and C5ORF42 genes has been associated with Adrenocortical 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 |
|---|---|---|---|---|
| SPEF2-C5ORF42-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-RERE | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-REOR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-REGO | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-REGR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-OROR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GORE | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GROR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| SPEF2-C5ORF42-20-AQAQ | 20 (40 μL) | 200 μL |
|
C5orf42 Gene Summary
The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]
Gene Name: Chromosome 5 Open Reading Frame 42
Chromosome: CHR5: 37106329 -37249530
Locus: 5p13.2
SPEF2 Gene Summary
The Sperm Flagellar 2 (SPEF2) gene is located on chr5 :35617988-35814713 at 5p13.2.
Gene Name: Sperm Flagellar 2
Chromosome: CHR5: 35617988 -35814713
Locus: 5p13.2
Gene Diseases
The SPEF2 C5ORF42 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Adrenocortical Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|