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FAM134B-SLC6A19 Fusion FISH Probe

The FAM134B-SLC6A19 Fusion FISH Probe is used to confirm a fusion of the FAM134B and SLC6A19 genes. The fusion of the FAM134B and SLC6A19 genes has been associated with Stomach Adenocarcinoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
FAM134B-SLC6A19-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-RERE 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-REOR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-REGO 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-REGR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-REAQ 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-ORRE 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-OROR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-ORGO 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-ORAQ 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GORE 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GOOR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GOGO 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GOGR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GOAQ 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GRRE 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GROR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GRGO 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GRGR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-GRAQ 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-AQRE 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-AQOR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-AQGO 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-AQGR 20 (40 μL) 200 μL
FAM134B-SLC6A19-20-AQAQ 20 (40 μL) 200 μL

SLC6A19 Gene Summary

This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]

Gene Name: Solute Carrier Family 6 Member 19

Chromosome: CHR5: 1201709 -1225230

Locus: 5p15.33

Gene Diseases

The FAM134B SLC6A19 Fusion has been associated with the following diseases:

Disease Name
Stomach Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.