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TC2N-FBLN5 Fusion FISH Probe

The TC2N-FBLN5 Fusion FISH Probe is used to confirm a fusion of the TC2N and FBLN5 genes. The fusion of the TC2N and FBLN5 genes has been associated with Breast Invasive Carcinoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

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

SKU Test Kits Buffer Dye Color Order Now
TC2N-FBLN5-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
TC2N-FBLN5-20-RERE 20 (40 μL) 200 μL
TC2N-FBLN5-20-REOR 20 (40 μL) 200 μL
TC2N-FBLN5-20-REGO 20 (40 μL) 200 μL
TC2N-FBLN5-20-REGR 20 (40 μL) 200 μL
TC2N-FBLN5-20-REAQ 20 (40 μL) 200 μL
TC2N-FBLN5-20-ORRE 20 (40 μL) 200 μL
TC2N-FBLN5-20-OROR 20 (40 μL) 200 μL
TC2N-FBLN5-20-ORGO 20 (40 μL) 200 μL
TC2N-FBLN5-20-ORAQ 20 (40 μL) 200 μL
TC2N-FBLN5-20-GORE 20 (40 μL) 200 μL
TC2N-FBLN5-20-GOOR 20 (40 μL) 200 μL
TC2N-FBLN5-20-GOGO 20 (40 μL) 200 μL
TC2N-FBLN5-20-GOGR 20 (40 μL) 200 μL
TC2N-FBLN5-20-GOAQ 20 (40 μL) 200 μL
TC2N-FBLN5-20-GRRE 20 (40 μL) 200 μL
TC2N-FBLN5-20-GROR 20 (40 μL) 200 μL
TC2N-FBLN5-20-GRGO 20 (40 μL) 200 μL
TC2N-FBLN5-20-GRGR 20 (40 μL) 200 μL
TC2N-FBLN5-20-GRAQ 20 (40 μL) 200 μL
TC2N-FBLN5-20-AQRE 20 (40 μL) 200 μL
TC2N-FBLN5-20-AQOR 20 (40 μL) 200 μL
TC2N-FBLN5-20-AQGO 20 (40 μL) 200 μL
TC2N-FBLN5-20-AQGR 20 (40 μL) 200 μL
TC2N-FBLN5-20-AQAQ 20 (40 μL) 200 μL

FBLN5 Gene Summary

The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3). [provided by RefSeq, Jul 2008]

Gene Name: Fibulin 5

Chromosome: CHR14: 92335754 -92414046

Locus: 14q32.12

TC2N Gene Summary

The Tandem C2 Domains, Nuclear (TC2N) gene is located on chr14 :92246266-92333880 at 14q32.12.

Gene Name: Tandem C2 Domains, Nuclear

Chromosome: CHR14: 92246266 -92333880

Locus: 14q32.12

Gene Diseases

The TC2N FBLN5 Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.