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ACTB-GLTSCR2 Fusion FISH Probe

The ACTB-GLTSCR2 Fusion FISH Probe is used to confirm a fusion of the ACTB and GLTSCR2 genes. The fusion of the ACTB and GLTSCR2 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
ACTB-GLTSCR2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-RERE 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-REOR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-REGO 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-REGR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-REAQ 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-ORRE 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-OROR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-ORGO 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-ORAQ 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GORE 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GOOR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GOGO 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GOGR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GOAQ 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GRRE 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GROR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GRGO 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GRGR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-GRAQ 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-AQRE 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-AQOR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-AQGO 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-AQGR 20 (40 μL) 200 μL
ACTB-GLTSCR2-20-AQAQ 20 (40 μL) 200 μL

ACTB Gene Summary

This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome. [provided by RefSeq, Aug 2017]

Gene Name: Actin Beta

Chromosome: CHR7: 5566778 -5570232

Locus: 7p22.1

Gene Diseases

The ACTB GLTSCR2 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.