KRT14 FISH Probe
The KRT14 gene, located on chromosome 17q21.2, encodes members of the keratin family that form the cytoskeleton of epithelial cells. KRT14 mutations are frequently observed in skin cancer, breast cancer, cervical cancer, thyroid hurthle cell adenoma, and ductal carcinoma in situ. Empire Genomics has developed a KRT14 FISH Probe assay which can be used to detect KRT14 gene aneusomy. The probe comes labeled in orange, and you may also choose to customize the probe to meet your needs.
** 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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| KRT14-20-OR (Standard Design) | 20 (40 μL) | 200 μL |
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| KRT14-20-GO | 20 (40 μL) | 200 μL |
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| KRT14-20-GR | 20 (40 μL) | 200 μL |
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| KRT14-20-AQ | 20 (40 μL) | 200 μL |
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| KRT14-20-RE | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a member of the keratin family, the most diverse group of intermediate filaments. This gene product, a type I keratin, is usually found as a heterotetramer with two keratin 5 molecules, a type II keratin. Together they form the cytoskeleton of epithelial cells. Mutations in the genes for these keratins are associated with epidermolysis bullosa simplex. At least one pseudogene has been identified at 17p12-p11. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: KRT14
Gene Name: Keratin 14
Chromosome: CHR17: 39738530-39743147
Locus: 17q21.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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