SLC16A10-NME7 Fusion FISH Probe
The SLC16A10-NME7 Fusion FISH Probe is used to confirm a fusion of the SLC16A10 and NME7 genes. The fusion of the SLC16A10 and NME7 genes has been associated with Cervical Squamous Cell Carcinoma And Endocervical 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 |
|---|---|---|---|---|
| SLC16A10-NME7-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-RERE | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-REOR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-REGO | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-REGR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-OROR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GORE | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GROR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| SLC16A10-NME7-20-AQAQ | 20 (40 μL) | 200 μL |
|
NME7 Gene Summary
This gene encodes a member of the non-metastatic expressed family of nucleoside diphosphate kinases. Members of this family are enzymes that catalyzes phosphate transfer from nucleoside triphosphates to nucleoside diphosphates. This protein contains two kinase domains, one of which is involved in autophosphorylation and the other may be inactive. This protein localizes to the centrosome and functions as a component of the gamma-tubulin ring complex which plays a role in microtubule organization. Mutations in this gene may be associated with venous thromboembolism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]
Gene Name: NME/NM23 Family Member 7
Chromosome: CHR1: 169101768 -169337186
Locus: 1q24.2
SLC16A10 Gene Summary
SLC16A10 is a member of a family of plasma membrane amino acid transporters that mediate the Na(+)-independent transport of aromatic amino acids across the plasma membrane.[supplied by OMIM, Apr 2004]
Gene Name: Solute Carrier Family 16 Member 10
Chromosome: CHR6: 111408780 -111544606
Locus: 6q21
Gene Diseases
The SLC16A10 NME7 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|