C15ORF41-MEIS2 Fusion FISH Probe
The C15ORF41-MEIS2 Fusion FISH Probe is used to confirm a fusion of the C15ORF41 and MEIS2 genes. The fusion of the C15ORF41 and MEIS2 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
C15ORF41-MEIS2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-RERE | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-REOR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-REGO | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-REGR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-REAQ | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-ORRE | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-OROR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-ORGO | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-ORAQ | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GORE | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GOOR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GOGO | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GOGR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GOAQ | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GRRE | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GROR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GRGO | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GRGR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-GRAQ | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-AQRE | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-AQOR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-AQGO | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-AQGR | 20 (40 μL) | 200 μL | ||
C15ORF41-MEIS2-20-AQAQ | 20 (40 μL) | 200 μL |
MEIS2 Gene Summary
This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. TALE homeobox proteins are highly conserved transcription regulators, and several members have been shown to be essential contributors to developmental programs. Multiple transcript variants encoding distinct isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Meis Homeobox 2
Chromosome: CHR15: 37183221 -37393500
Locus: 15q14
C15orf41 Gene Summary
This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
Gene Name: Chromosome 15 Open Reading Frame 41
Chromosome: CHR15: 36871811 -37102449
Locus: 15q14
Gene Diseases
The C15ORF41 MEIS2 Fusion has been associated with the following diseases:
Disease Name |
---|
Glioblastoma Multiforme |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
---|