CHCHD3-NUP205 Fusion FISH Probe
The CHCHD3-NUP205 Fusion FISH Probe is used to confirm a fusion of the CHCHD3 and NUP205 genes. The fusion of the CHCHD3 and NUP205 genes has been associated with Brain Lower Grade Glioma. 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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CHCHD3-NUP205-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-RERE | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-REOR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-REGO | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-REGR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-REAQ | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-ORRE | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-OROR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-ORGO | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-ORAQ | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GORE | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GOOR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GOGO | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GOGR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GOAQ | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GRRE | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GROR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GRGO | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GRGR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-GRAQ | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-AQRE | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-AQOR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-AQGO | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-AQGR | 20 (40 μL) | 200 μL | ||
CHCHD3-NUP205-20-AQAQ | 20 (40 μL) | 200 μL |
NUP205 Gene Summary
This gene encodes a nucleoporin, which is a subunit of the nuclear pore complex that functions in active transport of proteins, RNAs and ribonucleoprotein particles between the nucleus and cytoplasm. Mutations in this gene are associated with steroid-resistant nephrotic syndrome. [provided by RefSeq, Jul 2016]
Gene Name: Nucleoporin 205
Chromosome: CHR7: 135242661 -135333499
Locus: 7q33
CHCHD3 Gene Summary
The protein encoded by this gene is an inner mitochondrial membrane scaffold protein. Absence of the encoded protein affects the structural integrity of mitochondrial cristae and leads to reductions in ATP production, cell growth, and oxygen consumption. This protein is part of the mitochondrial contact site and cristae organizing system (MICOS). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]
Gene Name: Coiled-coil-helix-coiled-coil-helix Domain Containing 3
Chromosome: CHR7: 132469622 -132766828
Locus: 7q32.3-q33
Gene Diseases
The CHCHD3 NUP205 Fusion has been associated with the following diseases:
Disease Name |
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Brain Lower Grade Glioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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