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ABLIM1-PDE6B Fusion FISH Probe

The ABLIM1-PDE6B Fusion FISH Probe is used to confirm a fusion of the ABLIM1 and PDE6B genes. The fusion of the ABLIM1 and PDE6B genes has been associated with Uterine Corpus Endometrial 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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
ABLIM1-PDE6B-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-RERE 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-REOR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-REGO 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-REGR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-REAQ 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-ORRE 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-OROR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-ORGO 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-ORAQ 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GORE 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GOOR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GOGO 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GOGR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GOAQ 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GRRE 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GROR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GRGO 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GRGR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-GRAQ 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-AQRE 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-AQOR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-AQGO 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-AQGR 20 (40 μL) 200 μL
ABLIM1-PDE6B-20-AQAQ 20 (40 μL) 200 μL

ABLIM1 Gene Summary

This gene encodes a LIM zinc-binding domain-containing protein that binds to actin filaments and mediates interactions between actin and cytoplasmic targets. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2017]

Gene Name: Actin Binding LIM Protein 1

Chromosome: CHR10: 116190868 -116444414

Locus: 10q25.3

PDE6B Gene Summary

Photon absorption triggers a signaling cascade in rod photoreceptors that activates cGMP phosphodiesterase (PDE), resulting in the rapid hydrolysis of cGMP, closure of cGMP-gated cation channels, and hyperpolarization of the cell. PDE is a peripheral membrane heterotrimeric enzyme made up of alpha, beta, and gamma subunits. This gene encodes the beta subunit. Mutations in this gene result in retinitis pigmentosa and autosomal dominant congenital stationary night blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]

Gene Name: Phosphodiesterase 6B

Chromosome: CHR4: 619362 -664681

Locus: 4p16.3

Gene Diseases

The ABLIM1 PDE6B Fusion has been associated with the following diseases:

Disease Name
Uterine Corpus Endometrial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.