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KRT5-DSP Fusion FISH Probe

The KRT5-DSP Fusion FISH Probe is used to confirm a fusion of the KRT5 and DSP genes. The fusion of the KRT5 and DSP 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
KRT5-DSP-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KRT5-DSP-20-RERE 20 (40 μL) 200 μL
KRT5-DSP-20-REOR 20 (40 μL) 200 μL
KRT5-DSP-20-REGO 20 (40 μL) 200 μL
KRT5-DSP-20-REGR 20 (40 μL) 200 μL
KRT5-DSP-20-REAQ 20 (40 μL) 200 μL
KRT5-DSP-20-ORRE 20 (40 μL) 200 μL
KRT5-DSP-20-OROR 20 (40 μL) 200 μL
KRT5-DSP-20-ORGO 20 (40 μL) 200 μL
KRT5-DSP-20-ORAQ 20 (40 μL) 200 μL
KRT5-DSP-20-GORE 20 (40 μL) 200 μL
KRT5-DSP-20-GOOR 20 (40 μL) 200 μL
KRT5-DSP-20-GOGO 20 (40 μL) 200 μL
KRT5-DSP-20-GOGR 20 (40 μL) 200 μL
KRT5-DSP-20-GOAQ 20 (40 μL) 200 μL
KRT5-DSP-20-GRRE 20 (40 μL) 200 μL
KRT5-DSP-20-GROR 20 (40 μL) 200 μL
KRT5-DSP-20-GRGO 20 (40 μL) 200 μL
KRT5-DSP-20-GRGR 20 (40 μL) 200 μL
KRT5-DSP-20-GRAQ 20 (40 μL) 200 μL
KRT5-DSP-20-AQRE 20 (40 μL) 200 μL
KRT5-DSP-20-AQOR 20 (40 μL) 200 μL
KRT5-DSP-20-AQGO 20 (40 μL) 200 μL
KRT5-DSP-20-AQGR 20 (40 μL) 200 μL
KRT5-DSP-20-AQAQ 20 (40 μL) 200 μL

DSP Gene Summary

This gene encodes a protein that anchors intermediate filaments to desmosomal plaques and forms an obligate component of functional desmosomes. Mutations in this gene are the cause of several cardiomyopathies and keratodermas, including skin fragility-woolly hair syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

Gene Name: Desmoplakin

Chromosome: CHR6: 7541869 -7586946

Locus: 6p24.3

KRT5 Gene Summary

The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the basal layer of the epidermis with family member KRT14. Mutations in these genes have been associated with a complex of diseases termed epidermolysis bullosa simplex. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]

Gene Name: Keratin 5

Chromosome: CHR12: 52908358 -52914243

Locus: 12q13.13

Gene Diseases

The KRT5 DSP 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.