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SLC16A5-KCTD2 Fusion FISH Probe

The SLC16A5-KCTD2 Fusion FISH Probe is used to confirm a fusion of the SLC16A5 and KCTD2 genes. The fusion of the SLC16A5 and KCTD2 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. 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
SLC16A5-KCTD2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-RERE 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-REOR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-REGO 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-REGR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-REAQ 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-ORRE 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-OROR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-ORGO 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-ORAQ 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GORE 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GOOR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GOGO 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GOGR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GOAQ 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GRRE 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GROR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GRGO 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GRGR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-GRAQ 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-AQRE 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-AQOR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-AQGO 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-AQGR 20 (40 μL) 200 μL
SLC16A5-KCTD2-20-AQAQ 20 (40 μL) 200 μL

SLC16A5 Gene Summary

This gene encodes a member of the monocarboxylate transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

Gene Name: Solute Carrier Family 16 Member 5

Chromosome: CHR17: 73084054 -73102248

Locus: 17q25.1

KCTD2 Gene Summary

The Potassium Channel Tetramerization Domain Containing 2 (KCTD2) gene is located on chr17 :73043278-73061981 at 17q25.1.

Gene Name: Potassium Channel Tetramerization Domain Containing 2

Chromosome: CHR17: 73043278 -73061981

Locus: 17q25.1

Gene Diseases

The SLC16A5 KCTD2 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.