LPHN3-BBS9 Fusion FISH Probe
The LPHN3-BBS9 Fusion FISH Probe is used to confirm a fusion of the LPHN3 and BBS9 genes. The fusion of the LPHN3 and BBS9 genes has been associated with Lung Squamous Cell 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LPHN3-BBS9-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-RERE | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-REOR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-REGO | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-REGR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-OROR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GORE | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GROR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| LPHN3-BBS9-20-AQAQ | 20 (40 μL) | 200 μL |
|
BBS9 Gene Summary
This gene is downregulated by parathyroid hormone in osteoblastic cells, and therefore is thought to be involved in parathyroid hormone action in bones. The exact function of this gene has not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jan 2017]
Gene Name: Bardet-Biedl Syndrome 9
Chromosome: CHR7: 33169151 -33645680
Locus: 7p14.3
Gene Diseases
The LPHN3 BBS9 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|