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PHC3-SLC7A14 Fusion FISH Probe

The PHC3-SLC7A14 Fusion FISH Probe is used to confirm a fusion of the PHC3 and SLC7A14 genes. The fusion of the PHC3 and SLC7A14 genes has been associated with Liver Hepatocellular Carcinoma, Lung Squamous Cell Carcinoma, and Kidney Renal Papillary 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. 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
PHC3-SLC7A14-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
PHC3-SLC7A14-20-RERE 20 (40 μL) 200 μL
PHC3-SLC7A14-20-REOR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-REGO 20 (40 μL) 200 μL
PHC3-SLC7A14-20-REGR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-REAQ 20 (40 μL) 200 μL
PHC3-SLC7A14-20-ORRE 20 (40 μL) 200 μL
PHC3-SLC7A14-20-OROR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-ORGO 20 (40 μL) 200 μL
PHC3-SLC7A14-20-ORAQ 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GORE 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GOOR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GOGO 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GOGR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GOAQ 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GRRE 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GROR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GRGO 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GRGR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-GRAQ 20 (40 μL) 200 μL
PHC3-SLC7A14-20-AQRE 20 (40 μL) 200 μL
PHC3-SLC7A14-20-AQOR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-AQGO 20 (40 μL) 200 μL
PHC3-SLC7A14-20-AQGR 20 (40 μL) 200 μL
PHC3-SLC7A14-20-AQAQ 20 (40 μL) 200 μL

SLC7A14 Gene Summary

This gene is predicted to encode a glycosylated, cationic amino acid transporter protein with 14 transmembrane domains. This gene is primarily expressed in skin fibroblasts, neural tissue, and primary endothelial cells and its protein is predicted to mediate lysosomal uptake of cationic amino acids. Mutations in this gene are associated with autosomal recessive retinitis pigmentosa. In mice, this gene is expressed in the photoreceptor layer of the retina where its expression increases over the course of retinal development and persists in the mature retina. [provided by RefSeq, Apr 2014]

Gene Name: Solute Carrier Family 7 Member 14

Chromosome: CHR3: 170177341 -170303863

Locus: 3q26.2

PHC3 Gene Summary

The Polyhomeotic Homolog 3 (PHC3) gene is located on chr3 :169805367-169899537 at 3q26.2.

Gene Name: Polyhomeotic Homolog 3

Chromosome: CHR3: 169805367 -169899537

Locus: 3q26.2

Gene Diseases

The PHC3 SLC7A14 Fusion has been associated with the following diseases:

Disease Name
Liver Hepatocellular Carcinoma
Lung Squamous Cell Carcinoma
Kidney Renal Papillary 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.