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HMGCS1-UNC13A Fusion FISH Probe

The HMGCS1-UNC13A Fusion FISH Probe is used to confirm a fusion of the HMGCS1 and UNC13A genes. The fusion of the HMGCS1 and UNC13A 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
HMGCS1-UNC13A-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-RERE 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-REOR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-REGO 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-REGR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-REAQ 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-ORRE 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-OROR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-ORGO 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-ORAQ 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GORE 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GOOR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GOGO 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GOGR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GOAQ 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GRRE 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GROR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GRGO 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GRGR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-GRAQ 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-AQRE 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-AQOR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-AQGO 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-AQGR 20 (40 μL) 200 μL
HMGCS1-UNC13A-20-AQAQ 20 (40 μL) 200 μL

HMGCS1 Gene Summary

The 3-hydroxy-3-methylglutaryl-CoA Synthase 1 (HMGCS1) gene is located on chr5 :43289492-43313595 at 5p12.

Gene Name: 3-hydroxy-3-methylglutaryl-CoA Synthase 1

Chromosome: CHR5: 43289492 -43313595

Locus: 5p12

UNC13A Gene Summary

This gene encodes a member of the UNC13 family. UNC13 proteins bind to phorbol esters and diacylglycerol and play important roles in neurotransmitter release at synapses. Single nucleotide polymorphisms in this gene may be associated with sporadic amyotrophic lateral sclerosis. [provided by RefSeq, Feb 2012]

Gene Name: Unc-13 Homolog A

Chromosome: CHR19: 17712136 -17799008

Locus: 19p13.11

Gene Diseases

The HMGCS1 UNC13A 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.