MAN1A1-IFNGR2 Fusion FISH Probe
The MAN1A1-IFNGR2 Fusion FISH Probe is used to confirm a fusion of the MAN1A1 and IFNGR2 genes. The fusion of the MAN1A1 and IFNGR2 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MAN1A1-IFNGR2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| MAN1A1-IFNGR2-20-AQAQ | 20 (40 μL) | 200 μL |
|
IFNGR2 Gene Summary
This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance. [provided by RefSeq, Jul 2008]
Gene Name: Interferon Gamma Receptor 2
Chromosome: CHR21: 34775201 -34809828
Locus: 21q22.11
MAN1A1 Gene Summary
This gene encodes a class I mammalian Golgi 1,2-mannosidase which is a type II transmembrane protein. This protein catalyzes the hydrolysis of three terminal mannose residues from peptide-bound Man(9)-GlcNAc(2) oligosaccharides and belongs to family 47 of glycosyl hydrolases. [provided by RefSeq, Jul 2012]
Gene Name: Mannosidase Alpha Class 1A Member 1
Chromosome: CHR6: 119499266 -119670926
Locus: 6q22.31
Gene Diseases
The MAN1A1 IFNGR2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|