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KHDC1-SLC17A5 Fusion FISH Probe

The KHDC1-SLC17A5 Fusion FISH Probe is used to confirm a fusion of the KHDC1 and SLC17A5 genes. The fusion of the KHDC1 and SLC17A5 genes has been associated with Esophageal 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
KHDC1-SLC17A5-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-RERE 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-REOR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-REGO 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-REGR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-REAQ 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-ORRE 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-OROR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-ORGO 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-ORAQ 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GORE 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GOOR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GOGO 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GOGR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GOAQ 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GRRE 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GROR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GRGO 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GRGR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-GRAQ 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-AQRE 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-AQOR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-AQGO 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-AQGR 20 (40 μL) 200 μL
KHDC1-SLC17A5-20-AQAQ 20 (40 μL) 200 μL

SLC17A5 Gene Summary

This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]

Gene Name: Solute Carrier Family 17 Member 5

Chromosome: CHR6: 74303101 -74363737

Locus: 6q13

KHDC1 Gene Summary

The KH Domain Containing 1 (KHDC1) gene is located on chr6 :73951037-73972907 at 6q13.

Gene Name: KH Domain Containing 1

Chromosome: CHR6: 73951037 -73972907

Locus: 6q13

Gene Diseases

The KHDC1 SLC17A5 Fusion has been associated with the following diseases:

Disease Name
Esophageal Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.