TIMM22-C17ORF51 Fusion FISH Probe
The TIMM22-C17ORF51 Fusion FISH Probe is used to confirm a fusion of the TIMM22 and C17ORF51 genes. The fusion of the TIMM22 and C17ORF51 genes has been associated with Sarcoma. 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 |
|---|---|---|---|---|
| TIMM22-C17ORF51-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-RERE | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-REOR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-REGO | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-REGR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-OROR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GORE | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GROR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| TIMM22-C17ORF51-20-AQAQ | 20 (40 μL) | 200 μL |
|
TIMM22 Gene Summary
Multipass transmembrane proteins are brought into mitochondria and inserted into the mitochondrial inner membrane by way of the TIM22 complex. This complex has six subunits and is a twin-pore translocase. The protein encoded by this gene is a subunit of TIM22 and represents the voltage-activated and signal-gated channel. [provided by RefSeq, Jul 2016]
Gene Name: Translocase Of Inner Mitochondrial Membrane 22
Chromosome: CHR17: 900356 -905390
Locus: 17p13.3
C17orf51 Gene Summary
The Chromosome 17 Open Reading Frame 51 (C17orf51) gene is located on chr17 :21431570-21454941 at 17p11.2.
Gene Name: Chromosome 17 Open Reading Frame 51
Chromosome: CHR17: 21431570 -21454941
Locus: 17p11.2
Gene Diseases
The TIMM22 C17ORF51 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|