WASF2-IFI6 Fusion FISH Probe
The WASF2-IFI6 Fusion FISH Probe is used to confirm a fusion of the WASF2 and IFI6 genes. The fusion of the WASF2 and IFI6 genes has been associated with Esophageal 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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WASF2-IFI6-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-RERE | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-REOR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-REGO | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-REGR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-REAQ | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-ORRE | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-OROR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-ORGO | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-ORAQ | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GORE | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GOOR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GOGO | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GOGR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GOAQ | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GRRE | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GROR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GRGO | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GRGR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-GRAQ | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-AQRE | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-AQOR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-AQGO | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-AQGR | 20 (40 μL) | 200 μL | ||
WASF2-IFI6-20-AQAQ | 20 (40 μL) | 200 μL |
IFI6 Gene Summary
This gene was first identified as one of the many genes induced by interferon. The encoded protein may play a critical role in the regulation of apoptosis. A minisatellite that consists of 26 repeats of a 12 nucleotide repeating element resembling the mammalian splice donor consensus sequence begins near the end of the second exon. Alternatively spliced transcript variants that encode different isoforms by using the two downstream repeat units as splice donor sites have been described. [provided by RefSeq, Jul 2008]
Gene Name: Interferon Alpha Inducible Protein 6
Chromosome: CHR1: 27992571 -27998724
Locus: 1p35.3
WASF2 Gene Summary
This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. The published map location (PMID:10381382) has been changed based on recent genomic sequence comparisons, which indicate that the expressed gene is located on chromosome 1, and a pseudogene may be located on chromosome X. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
Gene Name: WAS Protein Family Member 2
Chromosome: CHR1: 27730733 -27816678
Locus: 1p36.11
Gene Diseases
The WASF2 IFI6 Fusion has been associated with the following diseases:
Disease Name |
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Esophageal Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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