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FGF13-NLRP3 Fusion FISH Probe

The FGF13-NLRP3 Fusion FISH Probe is used to confirm a fusion of the FGF13 and NLRP3 genes. The fusion of the FGF13 and NLRP3 genes has been associated with Breast Invasive 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.

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

SKU Test Kits Buffer Dye Color Order Now
FGF13-NLRP3-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FGF13-NLRP3-20-RERE 20 (40 μL) 200 μL
FGF13-NLRP3-20-REOR 20 (40 μL) 200 μL
FGF13-NLRP3-20-REGO 20 (40 μL) 200 μL
FGF13-NLRP3-20-REGR 20 (40 μL) 200 μL
FGF13-NLRP3-20-REAQ 20 (40 μL) 200 μL
FGF13-NLRP3-20-ORRE 20 (40 μL) 200 μL
FGF13-NLRP3-20-OROR 20 (40 μL) 200 μL
FGF13-NLRP3-20-ORGO 20 (40 μL) 200 μL
FGF13-NLRP3-20-ORAQ 20 (40 μL) 200 μL
FGF13-NLRP3-20-GORE 20 (40 μL) 200 μL
FGF13-NLRP3-20-GOOR 20 (40 μL) 200 μL
FGF13-NLRP3-20-GOGO 20 (40 μL) 200 μL
FGF13-NLRP3-20-GOGR 20 (40 μL) 200 μL
FGF13-NLRP3-20-GOAQ 20 (40 μL) 200 μL
FGF13-NLRP3-20-GRRE 20 (40 μL) 200 μL
FGF13-NLRP3-20-GROR 20 (40 μL) 200 μL
FGF13-NLRP3-20-GRGO 20 (40 μL) 200 μL
FGF13-NLRP3-20-GRGR 20 (40 μL) 200 μL
FGF13-NLRP3-20-GRAQ 20 (40 μL) 200 μL
FGF13-NLRP3-20-AQRE 20 (40 μL) 200 μL
FGF13-NLRP3-20-AQOR 20 (40 μL) 200 μL
FGF13-NLRP3-20-AQGO 20 (40 μL) 200 μL
FGF13-NLRP3-20-AQGR 20 (40 μL) 200 μL
FGF13-NLRP3-20-AQAQ 20 (40 μL) 200 μL

FGF13 Gene Summary

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]

Gene Name: Fibroblast Growth Factor 13

Chromosome: CHRX: 137713733 -138287185

Locus: Xq26.3-q27.1

NLRP3 Gene Summary

This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid. [provided by RefSeq, Oct 2008]

Gene Name: NLR Family Pyrin Domain Containing 3

Chromosome: CHR1: 247579457 -247612406

Locus: 1q44

Gene Diseases

The FGF13 NLRP3 Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.