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ACAD9-KIAA1257 Fusion FISH Probe

The ACAD9-KIAA1257 Fusion FISH Probe is used to confirm a fusion of the ACAD9 and KIAA1257 genes. The fusion of the ACAD9 and KIAA1257 genes has been associated with Brain Lower Grade Glioma. 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
ACAD9-KIAA1257-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-RERE 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-REOR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-REGO 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-REGR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-REAQ 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-ORRE 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-OROR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-ORGO 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-ORAQ 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GORE 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GOOR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GOGO 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GOGR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GOAQ 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GRRE 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GROR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GRGO 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GRGR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-GRAQ 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-AQRE 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-AQOR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-AQGO 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-AQGR 20 (40 μL) 200 μL
ACAD9-KIAA1257-20-AQAQ 20 (40 μL) 200 μL

ACAD9 Gene Summary

This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]

Gene Name: Acyl-CoA Dehydrogenase Family Member 9

Chromosome: CHR3: 128598332 -128631957

Locus: 3q21.3

KIAA1257 Gene Summary

The (KIAA1257) gene is located on chr3 :128689781-128712986 at 3q21.3.

Gene Name:

Chromosome: CHR3: 128689781 -128712986

Locus: 3q21.3

Gene Diseases

The ACAD9 KIAA1257 Fusion has been associated with the following diseases:

Disease Name
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.