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C3ORF72-PROS1 Fusion FISH Probe

The C3ORF72-PROS1 Fusion FISH Probe is used to confirm a fusion of the C3ORF72 and PROS1 genes. The fusion of the C3ORF72 and PROS1 genes has been associated with Skin Cutaneous Melanoma. 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
C3ORF72-PROS1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
C3ORF72-PROS1-20-RERE 20 (40 μL) 200 μL
C3ORF72-PROS1-20-REOR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-REGO 20 (40 μL) 200 μL
C3ORF72-PROS1-20-REGR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-REAQ 20 (40 μL) 200 μL
C3ORF72-PROS1-20-ORRE 20 (40 μL) 200 μL
C3ORF72-PROS1-20-OROR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-ORGO 20 (40 μL) 200 μL
C3ORF72-PROS1-20-ORAQ 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GORE 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GOOR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GOGO 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GOGR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GOAQ 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GRRE 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GROR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GRGO 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GRGR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-GRAQ 20 (40 μL) 200 μL
C3ORF72-PROS1-20-AQRE 20 (40 μL) 200 μL
C3ORF72-PROS1-20-AQOR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-AQGO 20 (40 μL) 200 μL
C3ORF72-PROS1-20-AQGR 20 (40 μL) 200 μL
C3ORF72-PROS1-20-AQAQ 20 (40 μL) 200 μL

PROS1 Gene Summary

This gene encodes a vitamin K-dependent plasma protein that functions as a cofactor for the anticoagulant protease, activated protein C (APC) to inhibit blood coagulation. It is found in plasma in both a free, functionally active form and also in an inactive form complexed with C4b-binding protein. Mutations in this gene result in autosomal dominant hereditary thrombophilia. An inactive pseudogene of this locus is located at an adjacent region on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Oct 2015]

Gene Name: Protein S

Chromosome: CHR3: 93591880 -93692934

Locus: 3q11.1

Gene Diseases

The C3ORF72 PROS1 Fusion has been associated with the following diseases:

Disease Name
Skin Cutaneous Melanoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.