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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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

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

Customer Publications

There are currently no FISH related publications for this probe.