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PSAP-C3 Fusion FISH Probe

The PSAP-C3 Fusion FISH Probe is used to confirm a fusion of the PSAP and C3 genes. The fusion of the PSAP and C3 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.

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

SKU Test Kits Buffer Dye Color Order Now
PSAP-C3-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
PSAP-C3-20-RERE 20 (40 μL) 200 μL
PSAP-C3-20-REOR 20 (40 μL) 200 μL
PSAP-C3-20-REGO 20 (40 μL) 200 μL
PSAP-C3-20-REGR 20 (40 μL) 200 μL
PSAP-C3-20-REAQ 20 (40 μL) 200 μL
PSAP-C3-20-ORRE 20 (40 μL) 200 μL
PSAP-C3-20-OROR 20 (40 μL) 200 μL
PSAP-C3-20-ORGO 20 (40 μL) 200 μL
PSAP-C3-20-ORAQ 20 (40 μL) 200 μL
PSAP-C3-20-GORE 20 (40 μL) 200 μL
PSAP-C3-20-GOOR 20 (40 μL) 200 μL
PSAP-C3-20-GOGO 20 (40 μL) 200 μL
PSAP-C3-20-GOGR 20 (40 μL) 200 μL
PSAP-C3-20-GOAQ 20 (40 μL) 200 μL
PSAP-C3-20-GRRE 20 (40 μL) 200 μL
PSAP-C3-20-GROR 20 (40 μL) 200 μL
PSAP-C3-20-GRGO 20 (40 μL) 200 μL
PSAP-C3-20-GRGR 20 (40 μL) 200 μL
PSAP-C3-20-GRAQ 20 (40 μL) 200 μL
PSAP-C3-20-AQRE 20 (40 μL) 200 μL
PSAP-C3-20-AQOR 20 (40 μL) 200 μL
PSAP-C3-20-AQGO 20 (40 μL) 200 μL
PSAP-C3-20-AQGR 20 (40 μL) 200 μL
PSAP-C3-20-AQAQ 20 (40 μL) 200 μL

C3 Gene Summary

Complement component C3 plays a central role in the activation of complement system. Its activation is required for both classical and alternative complement activation pathways. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form the mature protein, which is then further processed to generate numerous peptide products. The C3a peptide, also known as the C3a anaphylatoxin, modulates inflammation and possesses antimicrobial activity. Mutations in this gene are associated with atypical hemolytic uremic syndrome and age-related macular degeneration in human patients. [provided by RefSeq, Nov 2015]

Gene Name: Complement C3

Chromosome: CHR19: 6677845 -6720662

Locus: 19p13.3

PSAP Gene Summary

This gene encodes a highly conserved preproprotein that is proteolytically processed to generate four main cleavage products including saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]

Gene Name: Prosaposin

Chromosome: CHR10: 73576054 -73611082

Locus: 10q22.1

Gene Diseases

The PSAP C3 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.