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KRT13-THSD4 Fusion FISH Probe

The KRT13-THSD4 Fusion FISH Probe is used to confirm a fusion of the KRT13 and THSD4 genes. The fusion of the KRT13 and THSD4 genes has been associated with Cervical Squamous Cell Carcinoma And Endocervical 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.

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

SKU Test Kits Buffer Dye Color Order Now
KRT13-THSD4-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KRT13-THSD4-20-RERE 20 (40 μL) 200 μL
KRT13-THSD4-20-REOR 20 (40 μL) 200 μL
KRT13-THSD4-20-REGO 20 (40 μL) 200 μL
KRT13-THSD4-20-REGR 20 (40 μL) 200 μL
KRT13-THSD4-20-REAQ 20 (40 μL) 200 μL
KRT13-THSD4-20-ORRE 20 (40 μL) 200 μL
KRT13-THSD4-20-OROR 20 (40 μL) 200 μL
KRT13-THSD4-20-ORGO 20 (40 μL) 200 μL
KRT13-THSD4-20-ORAQ 20 (40 μL) 200 μL
KRT13-THSD4-20-GORE 20 (40 μL) 200 μL
KRT13-THSD4-20-GOOR 20 (40 μL) 200 μL
KRT13-THSD4-20-GOGO 20 (40 μL) 200 μL
KRT13-THSD4-20-GOGR 20 (40 μL) 200 μL
KRT13-THSD4-20-GOAQ 20 (40 μL) 200 μL
KRT13-THSD4-20-GRRE 20 (40 μL) 200 μL
KRT13-THSD4-20-GROR 20 (40 μL) 200 μL
KRT13-THSD4-20-GRGO 20 (40 μL) 200 μL
KRT13-THSD4-20-GRGR 20 (40 μL) 200 μL
KRT13-THSD4-20-GRAQ 20 (40 μL) 200 μL
KRT13-THSD4-20-AQRE 20 (40 μL) 200 μL
KRT13-THSD4-20-AQOR 20 (40 μL) 200 μL
KRT13-THSD4-20-AQGO 20 (40 μL) 200 μL
KRT13-THSD4-20-AQGR 20 (40 μL) 200 μL
KRT13-THSD4-20-AQAQ 20 (40 μL) 200 μL

KRT13 Gene Summary

The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been described. [provided by RefSeq, Jul 2008]

Gene Name: Keratin 13

Chromosome: CHR17: 39657232 -39661865

Locus: 17q21.2

THSD4 Gene Summary

The Thrombospondin Type 1 Domain Containing 4 (THSD4) gene is located on chr15 :71433787-72075722 at 15q23.

Gene Name: Thrombospondin Type 1 Domain Containing 4

Chromosome: CHR15: 71433787 -72075722

Locus: 15q23

Gene Diseases

The KRT13 THSD4 Fusion has been associated with the following diseases:

Disease Name
Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.