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TMEM87B-MERTK Fusion FISH Probe

The TMEM87B-MERTK Fusion FISH Probe is used to confirm a fusion of the TMEM87B and MERTK genes. The fusion of the TMEM87B and MERTK genes has been associated with Lung Adenocarcinoma, Lung Squamous Cell Carcinoma, Breast Invasive Carcinoma, Adrenocortical Carcinoma, and Bladder Urothelial 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
TMEM87B-MERTK-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
TMEM87B-MERTK-20-RERE 20 (40 μL) 200 μL
TMEM87B-MERTK-20-REOR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-REGO 20 (40 μL) 200 μL
TMEM87B-MERTK-20-REGR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-REAQ 20 (40 μL) 200 μL
TMEM87B-MERTK-20-ORRE 20 (40 μL) 200 μL
TMEM87B-MERTK-20-OROR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-ORGO 20 (40 μL) 200 μL
TMEM87B-MERTK-20-ORAQ 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GORE 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GOOR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GOGO 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GOGR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GOAQ 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GRRE 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GROR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GRGO 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GRGR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-GRAQ 20 (40 μL) 200 μL
TMEM87B-MERTK-20-AQRE 20 (40 μL) 200 μL
TMEM87B-MERTK-20-AQOR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-AQGO 20 (40 μL) 200 μL
TMEM87B-MERTK-20-AQGR 20 (40 μL) 200 μL
TMEM87B-MERTK-20-AQAQ 20 (40 μL) 200 μL

MERTK Gene Summary

This gene is a member of the MER/AXL/TYRO3 receptor kinase family and encodes a transmembrane protein with two fibronectin type-III domains, two Ig-like C2-type (immunoglobulin-like) domains, and one tyrosine kinase domain. Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP). [provided by RefSeq, Jul 2008]

Gene Name: MER Proto-oncogene, Tyrosine Kinase

Chromosome: CHR2: 112656190 -112786945

Locus: 2q13

TMEM87B Gene Summary

This gene encodes a protein that may interact with human papillomavirus type 18 E6 oncogene. The protein is also likely to be involved in endosome-to-trans-Golgi network retrograde transport. The gene is expressed in adult and fetal tissues, including brain and heart. This gene is a component of the 2q13 deletion syndrome. Mutations in this gene may be associated with congenital heart defects. [provided by RefSeq, Aug 2016]

Gene Name: Transmembrane Protein 87B

Chromosome: CHR2: 112812799 -112876895

Locus: 2q13

Gene Diseases

The TMEM87B MERTK Fusion has been associated with the following diseases:

Disease Name
Lung Adenocarcinoma
Lung Squamous Cell Carcinoma
Breast Invasive Carcinoma
Adrenocortical Carcinoma
Bladder Urothelial Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Genomic Fusions in Pigmented Spindle Cell Nevus of Reed

Pigmented spindle cell nevus (PSCN) of Reed is a type of Spitz nevus that can be difficult to diagnose. It is thought that gene fusions could be the basis of PSCN. The molecular characteristics of PSCN was under study with the use of RNA-sequencing and FISH. FISH analysis was performed with our MERTK and PITX3 fusion probes among other FISH tests. It was found that the majority of PSCN of Reed cases are the result of gene fusions, with the most frequent fusion involving NTRK3.