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NSUN5-BAZ1B Fusion FISH Probe

The NSUN5-BAZ1B Fusion FISH Probe is used to confirm a fusion of the NSUN5 and BAZ1B genes. The fusion of the NSUN5 and BAZ1B genes has been associated with Uterine Corpus Endometrial 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
NSUN5-BAZ1B-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-RERE 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-REOR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-REGO 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-REGR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-REAQ 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-ORRE 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-OROR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-ORGO 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-ORAQ 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GORE 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GOOR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GOGO 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GOGR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GOAQ 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GRRE 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GROR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GRGO 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GRGR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-GRAQ 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-AQRE 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-AQOR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-AQGO 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-AQGR 20 (40 μL) 200 μL
NSUN5-BAZ1B-20-AQAQ 20 (40 μL) 200 μL

BAZ1B Gene Summary

This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008]

Gene Name: Bromodomain Adjacent To Zinc Finger Domain 1B

Chromosome: CHR7: 72854727 -72936615

Locus: 7q11.23

NSUN5 Gene Summary

This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]

Gene Name: NOP2/Sun RNA Methyltransferase Family Member 5

Chromosome: CHR7: 72716513 -72722864

Locus: 7q11.23

Gene Diseases

The NSUN5 BAZ1B Fusion has been associated with the following diseases:

Disease Name
Uterine Corpus Endometrial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.