RBM10-PHF16 Fusion FISH Probe
The RBM10-PHF16 Fusion FISH Probe is used to confirm a fusion of the RBM10 and PHF16 genes. The fusion of the RBM10 and PHF16 genes has been associated with Breast Invasive 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. 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 |
|---|---|---|---|---|
| RBM10-PHF16-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-RERE | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-REOR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-REGO | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-REGR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-OROR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GORE | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GROR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| RBM10-PHF16-20-AQAQ | 20 (40 μL) | 200 μL |
|
RBM10 Gene Summary
This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]
Gene Name: RNA Binding Motif Protein 10
Chromosome: CHRX: 47004616 -47046214
Locus: Xp11.3
Gene Diseases
The RBM10 PHF16 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|