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CYTH3-GRID1 Fusion FISH Probe

The CYTH3-GRID1 Fusion FISH Probe is used to confirm a fusion of the CYTH3 and GRID1 genes. The fusion of the CYTH3 and GRID1 genes has been associated with Skin Cutaneous Melanoma. 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
CYTH3-GRID1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
CYTH3-GRID1-20-RERE 20 (40 μL) 200 μL
CYTH3-GRID1-20-REOR 20 (40 μL) 200 μL
CYTH3-GRID1-20-REGO 20 (40 μL) 200 μL
CYTH3-GRID1-20-REGR 20 (40 μL) 200 μL
CYTH3-GRID1-20-REAQ 20 (40 μL) 200 μL
CYTH3-GRID1-20-ORRE 20 (40 μL) 200 μL
CYTH3-GRID1-20-OROR 20 (40 μL) 200 μL
CYTH3-GRID1-20-ORGO 20 (40 μL) 200 μL
CYTH3-GRID1-20-ORAQ 20 (40 μL) 200 μL
CYTH3-GRID1-20-GORE 20 (40 μL) 200 μL
CYTH3-GRID1-20-GOOR 20 (40 μL) 200 μL
CYTH3-GRID1-20-GOGO 20 (40 μL) 200 μL
CYTH3-GRID1-20-GOGR 20 (40 μL) 200 μL
CYTH3-GRID1-20-GOAQ 20 (40 μL) 200 μL
CYTH3-GRID1-20-GRRE 20 (40 μL) 200 μL
CYTH3-GRID1-20-GROR 20 (40 μL) 200 μL
CYTH3-GRID1-20-GRGO 20 (40 μL) 200 μL
CYTH3-GRID1-20-GRGR 20 (40 μL) 200 μL
CYTH3-GRID1-20-GRAQ 20 (40 μL) 200 μL
CYTH3-GRID1-20-AQRE 20 (40 μL) 200 μL
CYTH3-GRID1-20-AQOR 20 (40 μL) 200 μL
CYTH3-GRID1-20-AQGO 20 (40 μL) 200 μL
CYTH3-GRID1-20-AQGR 20 (40 μL) 200 μL
CYTH3-GRID1-20-AQAQ 20 (40 μL) 200 μL

GRID1 Gene Summary

This gene encodes a subunit of glutamate receptor channels. These channels mediate most of the fast excitatory synaptic transmission in the central nervous system and play key roles in synaptic plasticity.[provided by RefSeq, Jan 2009]

Gene Name: Glutamate Ionotropic Receptor Delta Type Subunit 1

Chromosome: CHR10: 87359311 -88126250

Locus: 10q23.1-q23.2

CYTH3 Gene Summary

This gene encodes a member of the PSCD (pleckstrin homology, Sec7 and coiled-coil domains) family. PSCD family members have identical structural organization that consists of an N-terminal coiled-coil motif, a central Sec7 domain, and a C-terminal pleckstrin homology (PH) domain. The coiled-coil motif is involved in homodimerization, the Sec7 domain contains guanine-nucleotide exchange protein (GEP) activity, and the PH domain interacts with phospholipids and is responsible for association of PSCDs with membranes. Members of this family appear to mediate the regulation of protein sorting and membrane trafficking. This encoded protein is involved in the control of Golgi structure and function, and it may have a physiological role in regulating ADP-ribosylation factor protein 6 (ARF) functions, in addition to acting on ARF1. [provided by RefSeq, Jul 2008]

Gene Name: Cytohesin 3

Chromosome: CHR7: 6201411 -6312242

Locus: 7p22.1

Gene Diseases

The CYTH3 GRID1 Fusion has been associated with the following diseases:

Disease Name
Skin Cutaneous Melanoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.