HGSNAT-VSTM2B Fusion FISH Probe
The HGSNAT-VSTM2B Fusion FISH Probe is used to confirm a fusion of the HGSNAT and VSTM2B genes. The fusion of the HGSNAT and VSTM2B genes has been associated with Ovarian Serous Cystadenocarcinoma. 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 |
|---|---|---|---|---|
| HGSNAT-VSTM2B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-RERE | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-REOR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-REGO | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-REGR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-OROR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GORE | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GROR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| HGSNAT-VSTM2B-20-AQAQ | 20 (40 μL) | 200 μL |
|
HGSNAT Gene Summary
This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. [provided by RefSeq, Jan 2009]
Gene Name: Heparan-alpha-glucosaminide N-acetyltransferase
Chromosome: CHR8: 42995591 -43057970
Locus: 8p11.21-p11.1
VSTM2B Gene Summary
The V-set And Transmembrane Domain Containing 2B (VSTM2B) gene is located on chr19 :30017490-30055226 at 19q12.
Gene Name: V-set And Transmembrane Domain Containing 2B
Chromosome: CHR19: 30017490 -30055226
Locus: 19q12
Gene Diseases
The HGSNAT VSTM2B Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Ovarian Serous Cystadenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|