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DENND1A-ENG Fusion FISH Probe

The DENND1A-ENG Fusion FISH Probe is used to confirm a fusion of the DENND1A and ENG genes. The fusion of the DENND1A and ENG genes has been associated with Head And Neck Squamous Cell 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
DENND1A-ENG-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
DENND1A-ENG-20-RERE 20 (40 μL) 200 μL
DENND1A-ENG-20-REOR 20 (40 μL) 200 μL
DENND1A-ENG-20-REGO 20 (40 μL) 200 μL
DENND1A-ENG-20-REGR 20 (40 μL) 200 μL
DENND1A-ENG-20-REAQ 20 (40 μL) 200 μL
DENND1A-ENG-20-ORRE 20 (40 μL) 200 μL
DENND1A-ENG-20-OROR 20 (40 μL) 200 μL
DENND1A-ENG-20-ORGO 20 (40 μL) 200 μL
DENND1A-ENG-20-ORAQ 20 (40 μL) 200 μL
DENND1A-ENG-20-GORE 20 (40 μL) 200 μL
DENND1A-ENG-20-GOOR 20 (40 μL) 200 μL
DENND1A-ENG-20-GOGO 20 (40 μL) 200 μL
DENND1A-ENG-20-GOGR 20 (40 μL) 200 μL
DENND1A-ENG-20-GOAQ 20 (40 μL) 200 μL
DENND1A-ENG-20-GRRE 20 (40 μL) 200 μL
DENND1A-ENG-20-GROR 20 (40 μL) 200 μL
DENND1A-ENG-20-GRGO 20 (40 μL) 200 μL
DENND1A-ENG-20-GRGR 20 (40 μL) 200 μL
DENND1A-ENG-20-GRAQ 20 (40 μL) 200 μL
DENND1A-ENG-20-AQRE 20 (40 μL) 200 μL
DENND1A-ENG-20-AQOR 20 (40 μL) 200 μL
DENND1A-ENG-20-AQGO 20 (40 μL) 200 μL
DENND1A-ENG-20-AQGR 20 (40 μL) 200 μL
DENND1A-ENG-20-AQAQ 20 (40 μL) 200 μL

ENG Gene Summary

This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]

Gene Name: Endoglin

Chromosome: CHR9: 130577290 -130617047

Locus: 9q34.11

DENND1A Gene Summary

Clathrin (see MIM 118955)-mediated endocytosis is a major mechanism for internalization of proteins and lipids. Members of the connecdenn family, such as DENND1A, function as guanine nucleotide exchange factors (GEFs) for the early endosomal small GTPase RAB35 (MIM 604199) and bind to clathrin and clathrin adaptor protein-2 (AP2; see MIM 601024). Thus, connecdenns link RAB35 activation with the clathrin machinery (Marat and McPherson, 2010 [PubMed 20154091]).[supplied by OMIM, Nov 2010]

Gene Name: DENN Domain Containing 1A

Chromosome: CHR9: 126141932 -126692417

Locus: 9q33.3

Gene Diseases

The DENND1A ENG Fusion has been associated with the following diseases:

Disease Name
Head And Neck Squamous Cell Carcinoma 

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.