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MAST2-CLDN14 Fusion FISH Probe

The MAST2-CLDN14 Fusion FISH Probe is used to confirm a fusion of the MAST2 and CLDN14 genes. The fusion of the MAST2 and CLDN14 genes has been associated with Ovarian Serous Cystadenocarcinoma. 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
MAST2-CLDN14-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
MAST2-CLDN14-20-RERE 20 (40 μL) 200 μL
MAST2-CLDN14-20-REOR 20 (40 μL) 200 μL
MAST2-CLDN14-20-REGO 20 (40 μL) 200 μL
MAST2-CLDN14-20-REGR 20 (40 μL) 200 μL
MAST2-CLDN14-20-REAQ 20 (40 μL) 200 μL
MAST2-CLDN14-20-ORRE 20 (40 μL) 200 μL
MAST2-CLDN14-20-OROR 20 (40 μL) 200 μL
MAST2-CLDN14-20-ORGO 20 (40 μL) 200 μL
MAST2-CLDN14-20-ORAQ 20 (40 μL) 200 μL
MAST2-CLDN14-20-GORE 20 (40 μL) 200 μL
MAST2-CLDN14-20-GOOR 20 (40 μL) 200 μL
MAST2-CLDN14-20-GOGO 20 (40 μL) 200 μL
MAST2-CLDN14-20-GOGR 20 (40 μL) 200 μL
MAST2-CLDN14-20-GOAQ 20 (40 μL) 200 μL
MAST2-CLDN14-20-GRRE 20 (40 μL) 200 μL
MAST2-CLDN14-20-GROR 20 (40 μL) 200 μL
MAST2-CLDN14-20-GRGO 20 (40 μL) 200 μL
MAST2-CLDN14-20-GRGR 20 (40 μL) 200 μL
MAST2-CLDN14-20-GRAQ 20 (40 μL) 200 μL
MAST2-CLDN14-20-AQRE 20 (40 μL) 200 μL
MAST2-CLDN14-20-AQOR 20 (40 μL) 200 μL
MAST2-CLDN14-20-AQGO 20 (40 μL) 200 μL
MAST2-CLDN14-20-AQGR 20 (40 μL) 200 μL
MAST2-CLDN14-20-AQAQ 20 (40 μL) 200 μL

MAST2 Gene Summary

The Microtubule Associated Serine/threonine Kinase 2 (MAST2) gene is located on chr1 :46269284-46501796 at 1p34.1.

Gene Name: Microtubule Associated Serine/threonine Kinase 2

Chromosome: CHR1: 46269284 -46501796

Locus: 1p34.1

CLDN14 Gene Summary

Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands. The encoded protein also binds specifically to the WW domain of Yes-associated protein. Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness. It is also reported that four synonymous variants in this gene are associated with kidney stones and reduced bone mineral density. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2010]

Gene Name: Claudin 14

Chromosome: CHR21: 37832919 -37948867

Locus: 21q22.13

Gene Diseases

The MAST2 CLDN14 Fusion has been associated with the following diseases:

Disease Name
Ovarian Serous Cystadenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.