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FAM134B-SNTG2 Fusion FISH Probe

The FAM134B-SNTG2 Fusion FISH Probe is used to confirm a fusion of the FAM134B and SNTG2 genes. The fusion of the FAM134B and SNTG2 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
FAM134B-SNTG2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FAM134B-SNTG2-20-RERE 20 (40 μL) 200 μL
FAM134B-SNTG2-20-REOR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-REGO 20 (40 μL) 200 μL
FAM134B-SNTG2-20-REGR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-REAQ 20 (40 μL) 200 μL
FAM134B-SNTG2-20-ORRE 20 (40 μL) 200 μL
FAM134B-SNTG2-20-OROR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-ORGO 20 (40 μL) 200 μL
FAM134B-SNTG2-20-ORAQ 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GORE 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GOOR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GOGO 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GOGR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GOAQ 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GRRE 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GROR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GRGO 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GRGR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-GRAQ 20 (40 μL) 200 μL
FAM134B-SNTG2-20-AQRE 20 (40 μL) 200 μL
FAM134B-SNTG2-20-AQOR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-AQGO 20 (40 μL) 200 μL
FAM134B-SNTG2-20-AQGR 20 (40 μL) 200 μL
FAM134B-SNTG2-20-AQAQ 20 (40 μL) 200 μL

SNTG2 Gene Summary

This gene encodes a protein belonging to the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy. There is evidence of alternative splicing yet the full-length nature of these variants has not been described. [provided by RefSeq, Jul 2008]

Gene Name: Syntrophin Gamma 2

Chromosome: CHR2: 946553 -1371384

Locus: 2p25.3

Gene Diseases

The FAM134B SNTG2 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.