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EFCAB4B-C12ORF4 Fusion FISH Probe

The EFCAB4B-C12ORF4 Fusion FISH Probe is used to confirm a fusion of the EFCAB4B and C12ORF4 genes. The fusion of the EFCAB4B and C12ORF4 genes has been associated with Glioblastoma Multiforme. 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
EFCAB4B-C12ORF4-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-RERE 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-REOR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-REGO 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-REGR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-REAQ 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-ORRE 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-OROR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-ORGO 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-ORAQ 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GORE 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GOOR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GOGO 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GOGR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GOAQ 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GRRE 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GROR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GRGO 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GRGR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-GRAQ 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-AQRE 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-AQOR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-AQGO 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-AQGR 20 (40 μL) 200 μL
EFCAB4B-C12ORF4-20-AQAQ 20 (40 μL) 200 μL

C12orf4 Gene Summary

This gene is highly conserved from nematodes to humans. In rat, the orthologous gene encodes a cytoplasmic protein that is involved in mast cell degranulation. The human gene has been implicated in autosomal recessive intellectual disability. [provided by RefSeq, Sep 2016]

Gene Name: Chromosome 12 Open Reading Frame 4

Chromosome: CHR12: 4596900 -4647637

Locus: 12p13.32

Gene Diseases

The EFCAB4B C12ORF4 Fusion has been associated with the following diseases:

Disease Name
Glioblastoma Multiforme

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.