WASL-FEZF1 Fusion FISH Probe
The WASL-FEZF1 Fusion FISH Probe is used to confirm a fusion of the WASL and FEZF1 genes. The fusion of the WASL and FEZF1 genes has been associated with Prostate Adenocarcinoma. 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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WASL-FEZF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-RERE | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-REOR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-REGO | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-REGR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-REAQ | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-ORRE | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-OROR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-ORGO | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-ORAQ | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GORE | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GOOR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GOGO | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GOGR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GOAQ | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GRRE | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GROR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GRGO | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GRGR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-GRAQ | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-AQRE | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-AQOR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-AQGO | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-AQGR | 20 (40 μL) | 200 μL | ||
WASL-FEZF1-20-AQAQ | 20 (40 μL) | 200 μL |
WASL Gene Summary
This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family. Wiskott-Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin-related protein-2/3 (ARP2/3) complex. The encoded protein may be involved in the formation of long actin microspikes, and in neurite extension. [provided by RefSeq, Jul 2013]
Gene Name: Wiskott-Aldrich Syndrome Like
Chromosome: CHR7: 123321996 -123389116
Locus: 7q31.32
FEZF1 Gene Summary
This gene encodes a transcriptional repressor that belongs to the zinc finger double domain protein family. The encoded protein is thought to play a role in the embryonic migration of gonadotropin-releasing hormone neurons into the brain. Mutations in this gene are associated with hypogonadotropic hypogonadism-22 with anosmia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]
Gene Name: FEZ Family Zinc Finger 1
Chromosome: CHR7: 121941447 -121944565
Locus: 7q31.32
Gene Diseases
The WASL FEZF1 Fusion has been associated with the following diseases:
Disease Name |
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Prostate Adenocarcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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