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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| KRT13-THSD4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-RERE | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-REOR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-REGO | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-REGR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-REAQ | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-ORRE | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-OROR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-ORGO | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-ORAQ | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GORE | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GOOR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GOGO | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GOGR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GOAQ | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GRRE | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GROR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GRGO | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GRGR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-GRAQ | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-AQRE | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-AQOR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-AQGO | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-AQGR | 20 (40 μL) | 200 μL |
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| KRT13-THSD4-20-AQAQ | 20 (40 μL) | 200 μL |
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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 |
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| Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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