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KIFC3-CNGB1 Fusion FISH Probe

The KIFC3-CNGB1 Fusion FISH Probe is used to confirm a fusion of the KIFC3 and CNGB1 genes. The fusion of the KIFC3 and CNGB1 genes has been associated with Lung 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
KIFC3-CNGB1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
KIFC3-CNGB1-20-RERE 20 (40 μL) 200 μL
KIFC3-CNGB1-20-REOR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-REGO 20 (40 μL) 200 μL
KIFC3-CNGB1-20-REGR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-REAQ 20 (40 μL) 200 μL
KIFC3-CNGB1-20-ORRE 20 (40 μL) 200 μL
KIFC3-CNGB1-20-OROR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-ORGO 20 (40 μL) 200 μL
KIFC3-CNGB1-20-ORAQ 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GORE 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GOOR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GOGO 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GOGR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GOAQ 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GRRE 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GROR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GRGO 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GRGR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-GRAQ 20 (40 μL) 200 μL
KIFC3-CNGB1-20-AQRE 20 (40 μL) 200 μL
KIFC3-CNGB1-20-AQOR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-AQGO 20 (40 μL) 200 μL
KIFC3-CNGB1-20-AQGR 20 (40 μL) 200 μL
KIFC3-CNGB1-20-AQAQ 20 (40 μL) 200 μL

CNGB1 Gene Summary

In humans, the rod photoreceptor cGMP-gated cation channel helps regulate ion flow into the rod photoreceptor outer segment in response to light-induced alteration of the levels of intracellular cGMP. This channel consists of two subunits, alpha and beta, with the protein encoded by this gene representing the beta subunit. Defects in this gene are a cause of cause of retinitis pigmentosa type 45. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]

Gene Name: Cyclic Nucleotide Gated Channel Beta 1

Chromosome: CHR16: 57916243 -58005020

Locus: 16q21

KIFC3 Gene Summary

This gene encodes a member of the kinesin-14 family of microtubule motors. Members of this family play a role in the formation, maintenance and remodeling of the bipolar mitotic spindle. The protein encoded by this gene has cytoplasmic functions in the interphase cells. It may also be involved in the final stages of cytokinesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016]

Gene Name: Kinesin Family Member C3

Chromosome: CHR16: 57792128 -57836439

Locus: 16q21

Gene Diseases

The KIFC3 CNGB1 Fusion has been associated with the following diseases:

Disease Name
Lung Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.