ZDHHC9-SLCO1A2 Fusion FISH Probe
The ZDHHC9-SLCO1A2 Fusion FISH Probe is used to confirm a fusion of the ZDHHC9 and SLCO1A2 genes. The fusion of the ZDHHC9 and SLCO1A2 genes has been associated with Skin Cutaneous Melanoma. 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 |
|---|---|---|---|---|
| ZDHHC9-SLCO1A2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| ZDHHC9-SLCO1A2-20-AQAQ | 20 (40 μL) | 200 μL |
|
SLCO1A2 Gene Summary
This gene encodes a sodium-independent transporter which mediates cellular uptake of organic ions in the liver. Its substrates include bile acids, bromosulphophthalein, and some steroidal compounds. The protein is a member of the SLC21A family of solute carriers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2008]
Gene Name: Solute Carrier Organic Anion Transporter Family Member 1A2
Chromosome: CHR12: 21417533 -21548371
Locus: 12p12.1
ZDHHC9 Gene Summary
This gene encodes an integral membrane protein that is a member of the zinc finger DHHC domain-containing protein family. The encoded protein forms a complex with golgin subfamily A member 7 and functions as a palmitoyltransferase. This protein specifically palmitoylates HRAS and NRAS. Mutations in this gene are associated with X-linked cognitive disability. Alternate splicing results in multiple transcript variants that encode the same protein.[provided by RefSeq, May 2010]
Gene Name: Zinc Finger DHHC-type Containing 9
Chromosome: CHRX: 128937263 -128977910
Locus: Xq26.1
Gene Diseases
The ZDHHC9 SLCO1A2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|