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AUH-CPM Fusion FISH Probe

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

AUH Gene Summary

This gene encodes bifunctional mitochondrial protein that has both RNA-binding and hydratase activities. The encoded protein is a methylglutaconyl-CoA hydratase that catalyzes the hydration of 3-methylglutaconyl-CoA to 3-hydroxy-3-methyl-glutaryl-CoA, a critical step in the leucine degradation pathway. This protein also binds AU-rich elements (AREs) found in the 3' UTRs of rapidly decaying mRNAs including c-fos, c-myc and granulocyte/ macrophage colony stimulating factor. ARE elements are involved in directing RNA to rapid degradation and deadenylation. This protein is localizes to the mitochondrial matrix and the inner mitochondrial membrane and may be involved in mitochondrial protein synthesis. Mutations in this gene are the cause of 3-methylglutaconic aciduria, type I. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]

Gene Name: AU RNA Binding Methylglutaconyl-CoA Hydratase

Chromosome: CHR9: 93976096 -94124206

Locus: 9q22.31

CPM Gene Summary

The protein encoded by this gene is a membrane-bound arginine/lysine carboxypeptidase. Its expression is associated with monocyte to macrophage differentiation. This encoded protein contains hydrophobic regions at the amino and carboxy termini and has 6 potential asparagine-linked glycosylation sites. The active site residues of carboxypeptidases A and B are conserved in this protein. Three alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Carboxypeptidase M

Chromosome: CHR12: 69244955 -69357020

Locus: 12q15

Gene Diseases

The AUH CPM Fusion has been associated with the following diseases:

Disease Name
Sarcoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.