WHSC1L1-DDHD2 Fusion FISH Probe
The WHSC1L1-DDHD2 Fusion FISH Probe is used to confirm a fusion of the WHSC1L1 and DDHD2 genes. The fusion of the WHSC1L1 and DDHD2 genes has been associated with Lung Squamous Cell Carcinoma, and Pancreatic 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WHSC1L1-DDHD2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| WHSC1L1-DDHD2-20-AQAQ | 20 (40 μL) | 200 μL |
|
DDHD2 Gene Summary
This gene encodes a phospholipase enzyme containing sterile-alpha-motif (SAM), WWE, and DDHD domains. This protein participates in membrane trafficking between the endoplastic reticulum and the Golgi body. Mutations in this gene can cause autosomal recessive spastic paraplegia 54. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]
Gene Name: DDHD Domain Containing 2
Chromosome: CHR8: 38089008 -38120287
Locus: 8p11.23
Gene Diseases
The WHSC1L1 DDHD2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Lung Squamous Cell Carcinoma |
| Pancreatic Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|