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LUC7L2-MRPS33 Fusion FISH Probe

The LUC7L2-MRPS33 Fusion FISH Probe is used to confirm a fusion of the LUC7L2 and MRPS33 genes. The fusion of the LUC7L2 and MRPS33 genes has been associated with Prostate Adenocarcinoma. 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
LUC7L2-MRPS33-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-RERE 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-REOR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-REGO 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-REGR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-REAQ 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-ORRE 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-OROR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-ORGO 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-ORAQ 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GORE 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GOOR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GOGO 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GOGR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GOAQ 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GRRE 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GROR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GRGO 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GRGR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-GRAQ 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-AQRE 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-AQOR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-AQGO 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-AQGR 20 (40 μL) 200 μL
LUC7L2-MRPS33-20-AQAQ 20 (40 μL) 200 μL

LUC7L2 Gene Summary

This gene encodes a protein that contains a C2H2-type zinc finger, coiled-coil region and arginine, serine-rich (RS) domain. A similar protein in mouse interacts with sodium channel modifier 1, and the encoded protein may be involved in the recognition of non-consensus splice donor sites in association with the U1 snRNP spliceosomal subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]

Gene Name: LUC7 Like 2, Pre-mRNA Splicing Factor

Chromosome: CHR7: 139044633 -139108200

Locus: 7q34

MRPS33 Gene Summary

Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. The 28S subunit of the mammalian mitoribosome may play a crucial and characteristic role in translation initiation. This gene encodes a 28S subunit protein that is one of the more highly conserved mitochondrial ribosomal proteins among mammals, Drosophila and C. elegans. Splice variants that differ in the 5' UTR have been found for this gene; all variants encode the same protein. Pseudogenes corresponding to this gene are found on chromosomes 1q, 4p, 4q, and 20q [provided by RefSeq, Jul 2008]

Gene Name: Mitochondrial Ribosomal Protein S33

Chromosome: CHR7: 140705960 -140714781

Locus: 7q34

Gene Diseases

The LUC7L2 MRPS33 Fusion has been associated with the following diseases:

Disease Name
Prostate Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.