SEPT9 Break Apart FISH Probe
Empire Genomics’ SEPT9 Break Apart FISH Probe is designed to flank the SEPT9 gene and is typically used for detecting SEPT9 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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 |
|---|---|---|---|---|
| SEPT9BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-GROR | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| SEPT9BA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]
Gene Details
Gene Symbol: SEPT9
Gene Name: Septin 9
Chromosome: CHR17: 75277491-75496678
Locus: 17q25.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: SEPT9 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SEPT9-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping