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C2ORF67-ACADL Fusion FISH Probe

The C2ORF67-ACADL Fusion FISH Probe is used to confirm a fusion of the C2ORF67 and ACADL genes. The fusion of the C2ORF67 and ACADL genes has been associated with Kidney Renal Clear 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
C2ORF67-ACADL-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
C2ORF67-ACADL-20-RERE 20 (40 μL) 200 μL
C2ORF67-ACADL-20-REOR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-REGO 20 (40 μL) 200 μL
C2ORF67-ACADL-20-REGR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-REAQ 20 (40 μL) 200 μL
C2ORF67-ACADL-20-ORRE 20 (40 μL) 200 μL
C2ORF67-ACADL-20-OROR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-ORGO 20 (40 μL) 200 μL
C2ORF67-ACADL-20-ORAQ 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GORE 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GOOR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GOGO 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GOGR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GOAQ 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GRRE 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GROR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GRGO 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GRGR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-GRAQ 20 (40 μL) 200 μL
C2ORF67-ACADL-20-AQRE 20 (40 μL) 200 μL
C2ORF67-ACADL-20-AQOR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-AQGO 20 (40 μL) 200 μL
C2ORF67-ACADL-20-AQGR 20 (40 μL) 200 μL
C2ORF67-ACADL-20-AQAQ 20 (40 μL) 200 μL

ACADL Gene Summary

The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008]

Gene Name: Acyl-CoA Dehydrogenase Long Chain

Chromosome: CHR2: 211052715 -211090215

Locus: 2q34

Gene Diseases

The C2ORF67 ACADL Fusion has been associated with the following diseases:

Disease Name
Kidney Renal Clear 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.