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CCDC39-PECR Fusion FISH Probe

The CCDC39-PECR Fusion FISH Probe is used to confirm a fusion of the CCDC39 and PECR genes. The fusion of the CCDC39 and PECR genes has been associated with Sarcoma. 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
CCDC39-PECR-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
CCDC39-PECR-20-RERE 20 (40 μL) 200 μL
CCDC39-PECR-20-REOR 20 (40 μL) 200 μL
CCDC39-PECR-20-REGO 20 (40 μL) 200 μL
CCDC39-PECR-20-REGR 20 (40 μL) 200 μL
CCDC39-PECR-20-REAQ 20 (40 μL) 200 μL
CCDC39-PECR-20-ORRE 20 (40 μL) 200 μL
CCDC39-PECR-20-OROR 20 (40 μL) 200 μL
CCDC39-PECR-20-ORGO 20 (40 μL) 200 μL
CCDC39-PECR-20-ORAQ 20 (40 μL) 200 μL
CCDC39-PECR-20-GORE 20 (40 μL) 200 μL
CCDC39-PECR-20-GOOR 20 (40 μL) 200 μL
CCDC39-PECR-20-GOGO 20 (40 μL) 200 μL
CCDC39-PECR-20-GOGR 20 (40 μL) 200 μL
CCDC39-PECR-20-GOAQ 20 (40 μL) 200 μL
CCDC39-PECR-20-GRRE 20 (40 μL) 200 μL
CCDC39-PECR-20-GROR 20 (40 μL) 200 μL
CCDC39-PECR-20-GRGO 20 (40 μL) 200 μL
CCDC39-PECR-20-GRGR 20 (40 μL) 200 μL
CCDC39-PECR-20-GRAQ 20 (40 μL) 200 μL
CCDC39-PECR-20-AQRE 20 (40 μL) 200 μL
CCDC39-PECR-20-AQOR 20 (40 μL) 200 μL
CCDC39-PECR-20-AQGO 20 (40 μL) 200 μL
CCDC39-PECR-20-AQGR 20 (40 μL) 200 μL
CCDC39-PECR-20-AQAQ 20 (40 μL) 200 μL

PECR Gene Summary

The Peroxisomal Trans-2-enoyl-CoA Reductase (PECR) gene is located on chr2 :216903110-216946539 at 2q35.

Gene Name: Peroxisomal Trans-2-enoyl-CoA Reductase

Chromosome: CHR2: 216903110 -216946539

Locus: 2q35

CCDC39 Gene Summary

The protein encoded by this gene is involved in the motility of cilia and flagella. The encoded protein is essential for the assembly of dynein regulatory and inner dynein arm complexes, which regulate ciliary beat. Defects in this gene are a cause of primary ciliary dyskinesia type 14 (CILD14). [provided by RefSeq, Jul 2011]

Gene Name: Coiled-coil Domain Containing 39

Chromosome: CHR3: 180331795 -180397283

Locus: 3q26.33

Gene Diseases

The CCDC39 PECR Fusion has been associated with the following diseases:

Disease Name
Sarcoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.