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KCNQ5-CRYL1 Fusion FISH Probe

The KCNQ5-CRYL1 Fusion FISH Probe is used to confirm a fusion of the KCNQ5 and CRYL1 genes. The fusion of the KCNQ5 and CRYL1 genes has been associated with Bladder Urothelial 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
KCNQ5-CRYL1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-RERE 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-REOR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-REGO 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-REGR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-REAQ 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-ORRE 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-OROR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-ORGO 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-ORAQ 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GORE 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GOOR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GOGO 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GOGR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GOAQ 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GRRE 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GROR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GRGO 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GRGR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-GRAQ 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-AQRE 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-AQOR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-AQGO 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-AQGR 20 (40 μL) 200 μL
KCNQ5-CRYL1-20-AQAQ 20 (40 μL) 200 μL

CRYL1 Gene Summary

The uronate cycle functions as an alternative glucose metabolic pathway, accounting for about 5% of daily glucose catabolism. The product of this gene catalyzes the dehydrogenation of L-gulonate into dehydro-L-gulonate in the uronate cycle. The enzyme requires NAD(H) as a coenzyme, and is inhibited by inorganic phosphate. A similar gene in the rabbit is thought to serve a structural role in the lens of the eye. [provided by RefSeq, Jul 2008]

Gene Name: Crystallin Lambda 1

Chromosome: CHR13: 20977805 -21100012

Locus: 13q12.11

KCNQ5 Gene Summary

This gene is a member of the KCNQ potassium channel gene family that is differentially expressed in subregions of the brain and in skeletal muscle. The protein encoded by this gene yields currents that activate slowly with depolarization and can form heteromeric channels with the protein encoded by the KCNQ3 gene. Currents expressed from this protein have voltage dependences and inhibitor sensitivities in common with M-currents. They are also inhibited by M1 muscarinic receptor activation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

Gene Name: Potassium Voltage-gated Channel Subfamily Q Member 5

Chromosome: CHR6: 73331570 -73908573

Locus: 6q13

Gene Diseases

The KCNQ5 CRYL1 Fusion has been associated with the following diseases:

Disease Name
Bladder Urothelial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.