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NUMA1-CLPB Fusion FISH Probe

The NUMA1-CLPB Fusion FISH Probe is used to confirm a fusion of the NUMA1 and CLPB genes. The fusion of the NUMA1 and CLPB genes has been associated with Stomach 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
NUMA1-CLPB-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
NUMA1-CLPB-20-RERE 20 (40 μL) 200 μL
NUMA1-CLPB-20-REOR 20 (40 μL) 200 μL
NUMA1-CLPB-20-REGO 20 (40 μL) 200 μL
NUMA1-CLPB-20-REGR 20 (40 μL) 200 μL
NUMA1-CLPB-20-REAQ 20 (40 μL) 200 μL
NUMA1-CLPB-20-ORRE 20 (40 μL) 200 μL
NUMA1-CLPB-20-OROR 20 (40 μL) 200 μL
NUMA1-CLPB-20-ORGO 20 (40 μL) 200 μL
NUMA1-CLPB-20-ORAQ 20 (40 μL) 200 μL
NUMA1-CLPB-20-GORE 20 (40 μL) 200 μL
NUMA1-CLPB-20-GOOR 20 (40 μL) 200 μL
NUMA1-CLPB-20-GOGO 20 (40 μL) 200 μL
NUMA1-CLPB-20-GOGR 20 (40 μL) 200 μL
NUMA1-CLPB-20-GOAQ 20 (40 μL) 200 μL
NUMA1-CLPB-20-GRRE 20 (40 μL) 200 μL
NUMA1-CLPB-20-GROR 20 (40 μL) 200 μL
NUMA1-CLPB-20-GRGO 20 (40 μL) 200 μL
NUMA1-CLPB-20-GRGR 20 (40 μL) 200 μL
NUMA1-CLPB-20-GRAQ 20 (40 μL) 200 μL
NUMA1-CLPB-20-AQRE 20 (40 μL) 200 μL
NUMA1-CLPB-20-AQOR 20 (40 μL) 200 μL
NUMA1-CLPB-20-AQGO 20 (40 μL) 200 μL
NUMA1-CLPB-20-AQGR 20 (40 μL) 200 μL
NUMA1-CLPB-20-AQAQ 20 (40 μL) 200 μL

NUMA1 Gene Summary

This gene encodes a large protein that forms a structural component of the nuclear matrix. The encoded protein interacts with microtubules and plays a role in the formation and organization of the mitotic spindle during cell division. Chromosomal translocation of this gene with the RARA (retinoic acid receptor, alpha) gene on chromosome 17 have been detected in patients with acute promyelocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]

Gene Name: Nuclear Mitotic Apparatus Protein 1

Chromosome: CHR11: 71713910 -71791573

Locus: 11q13.4

CLPB Gene Summary

This gene belongs to the ATP-ases associated with diverse cellular activities (AAA+) superfamily. Members of this superfamily form ring-shaped homo-hexamers and have highly conserved ATPase domains that are involved in various processes including DNA replication, protein degradation and reactivation of misfolded proteins. All members of this family hydrolyze ATP through their AAA+ domains and use the energy generated through ATP hydrolysis to exert mechanical force on their substrates. In addition to an AAA+ domain, the protein encoded by this gene contains a C-terminal D2 domain, which is characteristic of the AAA+ subfamily of Caseinolytic peptidases to which this protein belongs. It cooperates with Hsp70 in the disaggregation of protein aggregates. Allelic variants of this gene are associated with 3-methylglutaconic aciduria, which causes cataracts and neutropenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]

Gene Name: ClpB Homolog, Mitochondrial AAA ATPase Chaperonin

Chromosome: CHR11: 72003469 -72145568

Locus: 11q13.4

Gene Diseases

The NUMA1 CLPB Fusion has been associated with the following diseases:

Disease Name
Stomach Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.