SLC25A13-SH2D3C Fusion FISH Probe
The SLC25A13-SH2D3C Fusion FISH Probe is used to confirm a fusion of the SLC25A13 and SH2D3C genes. The fusion of the SLC25A13 and SH2D3C genes has been associated with Pheochromocytoma And Paraganglioma. 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 |
|---|---|---|---|---|
| SLC25A13-SH2D3C-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-RERE | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-REOR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-REGO | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-REGR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-OROR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GORE | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GROR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| SLC25A13-SH2D3C-20-AQAQ | 20 (40 μL) | 200 μL |
|
SH2D3C Gene Summary
This gene encodes an adaptor protein and member of a cytoplasmic protein family involved in cell migration. The encoded protein contains a putative Src homology 2 (SH2) domain and guanine nucleotide exchange factor-like domain which allows this signaling protein to form a complex with scaffolding protein Crk-associated substrate. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2011]
Gene Name: SH2 Domain Containing 3C
Chromosome: CHR9: 130500595 -130541048
Locus: 9q34.11
SLC25A13 Gene Summary
This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Gene Name: Solute Carrier Family 25 Member 13
Chromosome: CHR7: 95749531 -95951459
Locus: 7q21.3
Gene Diseases
The SLC25A13 SH2D3C Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|