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SLC16A7-HOXC13 Fusion FISH Probe

The SLC16A7-HOXC13 Fusion FISH Probe is used to confirm a fusion of the SLC16A7 and HOXC13 genes. The fusion of the SLC16A7 and HOXC13 genes has been associated with Bladder Urothelial 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
SLC16A7-HOXC13-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-RERE 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-REOR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-REGO 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-REGR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-REAQ 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-ORRE 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-OROR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-ORGO 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-ORAQ 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GORE 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GOOR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GOGO 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GOGR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GOAQ 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GRRE 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GROR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GRGO 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GRGR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-GRAQ 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-AQRE 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-AQOR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-AQGO 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-AQGR 20 (40 μL) 200 μL
SLC16A7-HOXC13-20-AQAQ 20 (40 μL) 200 μL

HOXC13 Gene Summary

This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, which are located on different chromosomes and consist of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role in the development of hair, nail, and filiform papilla. [provided by RefSeq, Jul 2008]

Gene Name: Homeobox C13

Chromosome: CHR12: 54332575 -54340328

Locus: 12q13.13

SLC16A7 Gene Summary

This gene is a member of the monocarboxylate transporter family. Members in this family transport metabolites, such as lactate, pyruvate, and ketone bodies. The protein encoded by this gene catalyzes the proton-linked transport of monocarboxylates and has the highest affinity for pyruvate. This protein has been reported to be more highly expressed in prostate and colorectal cancer specimens when compared to control specimens. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]

Gene Name: Solute Carrier Family 16 Member 7

Chromosome: CHR12: 60083125 -60175408

Locus: 12q14.1

Gene Diseases

The SLC16A7 HOXC13 Fusion has been associated with the following diseases:

Disease Name
Bladder Urothelial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.