WNK1-KDM4B Fusion FISH Probe
The WNK1-KDM4B Fusion FISH Probe is used to confirm a fusion of the WNK1 and KDM4B genes. The fusion of the WNK1 and KDM4B genes has been associated with Head And Neck 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 |
|---|---|---|---|---|
| WNK1-KDM4B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-RERE | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-REOR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-REGO | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-REGR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-OROR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GORE | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GROR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| WNK1-KDM4B-20-AQAQ | 20 (40 μL) | 200 μL |
|
KDM4B Gene Summary
The Lysine Demethylase 4B (KDM4B) gene is located on chr19 :4969123-5153608 at 19p13.3.
Gene Name: Lysine Demethylase 4B
Chromosome: CHR19: 4969123 -5153608
Locus: 19p13.3
WNK1 Gene Summary
This gene encodes a member of the WNK subfamily of serine/threonine protein kinases. The encoded protein may be a key regulator of blood pressure by controlling the transport of sodium and chloride ions. Mutations in this gene have been associated with pseudohypoaldosteronism type II and hereditary sensory neuropathy type II. Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined.[provided by RefSeq, May 2010]
Gene Name: WNK Lysine Deficient Protein Kinase 1
Chromosome: CHR12: 862088 -1020618
Locus: 12p13.33
Gene Diseases
The WNK1 KDM4B Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|