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KIAA0556-NECAB2 Fusion FISH Probe

The KIAA0556-NECAB2 Fusion FISH Probe is used to confirm a fusion of the KIAA0556 and NECAB2 genes. The fusion of the KIAA0556 and NECAB2 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
KIAA0556-NECAB2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-RERE 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-REOR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-REGO 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-REGR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-REAQ 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-ORRE 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-OROR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-ORGO 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-ORAQ 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GORE 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GOOR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GOGO 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GOGR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GOAQ 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GRRE 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GROR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GRGO 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GRGR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-GRAQ 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-AQRE 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-AQOR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-AQGO 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-AQGR 20 (40 μL) 200 μL
KIAA0556-NECAB2-20-AQAQ 20 (40 μL) 200 μL

KIAA0556 Gene Summary

This gene encodes a novel, evolutionarily conserved, ciliary protein. In human hTERT-RPE1 cells, the protein is found at the base of cilia, decorating the ciliary axoneme, and enriched at the ciliary tip. The protein binds to microtubules in vitro and regulates their stability when it is overexpressed. A null mutation in this gene has been associated with Joubert syndrome, a recessive disorder that is characterized by a distinctive mid-hindbrain and cerebellar malformation and is also often associated with wider ciliopathy symptoms. Consistently, in a serum-starvation ciliogenesis assay, human fibroblast cells derived from patients with the mutation display a reduced number of ciliated cells with abnormally long cilia. [provided by RefSeq, Feb 2016]

Gene Name:

Chromosome: CHR16: 27561467 -27791692

Locus: 16p12.1

NECAB2 Gene Summary

The protein encoded by this gene is a neuronal calcium-binding protein that binds to and modulates the function of at least two receptors, adenosine A(2A) receptor and metabotropic glutamate receptor type 5. [provided by RefSeq, Jul 2016]

Gene Name: N-terminal EF-hand Calcium Binding Protein 2

Chromosome: CHR16: 84002236 -84036379

Locus: 16q23.3

Gene Diseases

The KIAA0556 NECAB2 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.