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NSD1-NUP98 Fusion FISH Probe

The NSD1-NUP98 Fusion FISH Probe is used to confirm a fusion of the NSD1 and NUP98 genes. The fusion of the NSD1 and NUP98 genes has been associated with Acute Myeloid Leukemia. 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
NSD1-NUP98-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
NSD1-NUP98-20-RERE 20 (40 μL) 200 μL
NSD1-NUP98-20-REOR 20 (40 μL) 200 μL
NSD1-NUP98-20-REGO 20 (40 μL) 200 μL
NSD1-NUP98-20-REGR 20 (40 μL) 200 μL
NSD1-NUP98-20-REAQ 20 (40 μL) 200 μL
NSD1-NUP98-20-ORRE 20 (40 μL) 200 μL
NSD1-NUP98-20-OROR 20 (40 μL) 200 μL
NSD1-NUP98-20-ORGO 20 (40 μL) 200 μL
NSD1-NUP98-20-ORAQ 20 (40 μL) 200 μL
NSD1-NUP98-20-GORE 20 (40 μL) 200 μL
NSD1-NUP98-20-GOOR 20 (40 μL) 200 μL
NSD1-NUP98-20-GOGO 20 (40 μL) 200 μL
NSD1-NUP98-20-GOGR 20 (40 μL) 200 μL
NSD1-NUP98-20-GOAQ 20 (40 μL) 200 μL
NSD1-NUP98-20-GRRE 20 (40 μL) 200 μL
NSD1-NUP98-20-GROR 20 (40 μL) 200 μL
NSD1-NUP98-20-GRGO 20 (40 μL) 200 μL
NSD1-NUP98-20-GRGR 20 (40 μL) 200 μL
NSD1-NUP98-20-GRAQ 20 (40 μL) 200 μL
NSD1-NUP98-20-AQRE 20 (40 μL) 200 μL
NSD1-NUP98-20-AQOR 20 (40 μL) 200 μL
NSD1-NUP98-20-AQGO 20 (40 μL) 200 μL
NSD1-NUP98-20-AQGR 20 (40 μL) 200 μL
NSD1-NUP98-20-AQAQ 20 (40 μL) 200 μL

NUP98 Gene Summary

Nuclear pore complexes (NPCs) regulate the transport of macromolecules between the nucleus and cytoplasm, and are composed of many polypeptide subunits, many of which belong to the nucleoporin family. This gene belongs to the nucleoporin gene family and encodes a 186 kDa precursor protein that undergoes autoproteolytic cleavage to generate a 98 kDa nucleoporin and 96 kDa nucleoporin. The 98 kDa nucleoporin contains a Gly-Leu-Phe-Gly (GLGF) repeat domain and participates in many cellular processes, including nuclear import, nuclear export, mitotic progression, and regulation of gene expression. The 96 kDa nucleoporin is a scaffold component of the NPC. Proteolytic cleavage is important for targeting of the proteins to the NPC. Translocations between this gene and many other partner genes have been observed in different leukemias. Rearrangements typically result in chimeras with the N-terminal GLGF domain of this gene to the C-terminus of the partner gene. Alternative splicing results in multiple transcript variants encoding different isoforms, at least two of which are proteolytically processed. Some variants lack the region that encodes the 96 kDa nucleoporin. [provided by RefSeq, Feb 2016]

Gene Name: Nucleoporin 98

Chromosome: CHR11: 3696239 -3819022

Locus: 11p15.4

NSD1 Gene Summary

This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Nuclear Receptor Binding SET Domain Protein 1

Chromosome: CHR5: 176560079 -176727214

Locus: 5q35.3

Gene Diseases

The NSD1 NUP98 Fusion has been associated with the following diseases:

Disease Name
Acute Myeloid Leukemia

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing

Detection of chromosomal translocations has proven crucial for diagnosis and management of acute myeloid leukemia (AML), a cancer known to harbor several distinct gene rearrangements that correlate with disease subtype. In this study, an AML patient was genetically profiled using both conventional karyotyping and next generation sequencing techniques. FISH was also used to detect NUP98 translocations using Empire Genomics’ NUP98 break-apart probe.