RWDD2B-MX2 Fusion FISH Probe
The RWDD2B-MX2 Fusion FISH Probe is used to confirm a fusion of the RWDD2B and MX2 genes. The fusion of the RWDD2B and MX2 genes has been associated with Bladder Urothelial 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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RWDD2B-MX2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-RERE | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-REOR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-REGO | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-REGR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-REAQ | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-ORRE | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-OROR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-ORGO | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-ORAQ | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GORE | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GOOR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GOGO | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GOGR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GOAQ | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GRRE | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GROR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GRGO | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GRGR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-GRAQ | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-AQRE | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-AQOR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-AQGO | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-AQGR | 20 (40 μL) | 200 μL | ||
RWDD2B-MX2-20-AQAQ | 20 (40 μL) | 200 μL |
MX2 Gene Summary
The protein encoded by this gene has a nuclear and a cytoplasmic form and is a member of both the dynamin family and the family of large GTPases. The nuclear form is localized in a granular pattern in the heterochromatin region beneath the nuclear envelope. A nuclear localization signal (NLS) is present at the amino terminal end of the nuclear form but is lacking in the cytoplasmic form due to use of an alternate translation start codon. This protein is upregulated by interferon-alpha but does not contain the antiviral activity of a similar myxovirus resistance protein 1. [provided by RefSeq, Jul 2008]
Gene Name: MX Dynamin Like GTPase 2
Chromosome: CHR21: 42733949 -42780869
Locus: 21q22.3
RWDD2B Gene Summary
The RWD Domain Containing 2B (RWDD2B) gene is located on chr21 :30378079-30391685 at 21q21.3.
Gene Name: RWD Domain Containing 2B
Chromosome: CHR21: 30378079 -30391685
Locus: 21q21.3
Gene Diseases
The RWDD2B MX2 Fusion has been associated with the following diseases:
Disease Name |
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Bladder Urothelial Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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