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NUMA1-PTH Fusion FISH Probe

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

PTH Gene Summary

This gene encodes a member of the parathyroid family of proteins. The encoded preproprotein is proteolytically processed to generate a protein that binds to the parathyroid hormone/parathyroid hormone-related peptide receptor and regulates blood calcium and phosphate levels. Excess production of the encoded protein, known as hyperparathyroidism, can result in hypercalcemia and kidney stones. On the other hand, defective processing of the encoded protein may lead to hypoparathyroidism, which can result in hypocalcemia and numbness. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]

Gene Name: Parathyroid Hormone

Chromosome: CHR11: 13513600 -13517567

Locus: 11p15.3

Gene Diseases

The NUMA1 PTH 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.