NAT8L-DBNDD1 Fusion FISH Probe
The NAT8L-DBNDD1 Fusion FISH Probe is used to confirm a fusion of the NAT8L and DBNDD1 genes. The fusion of the NAT8L and DBNDD1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| NAT8L-DBNDD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-RERE | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-REOR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-REGO | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-REGR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-REAQ | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-ORRE | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-OROR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-ORGO | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GORE | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GOOR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GOGO | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GOGR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GRRE | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GROR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GRGO | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GRGR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-AQRE | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-AQOR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-AQGO | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-AQGR | 20 (40 μL) | 200 μL |
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| NAT8L-DBNDD1-20-AQAQ | 20 (40 μL) | 200 μL |
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DBNDD1 Gene Summary
The Dysbindin Domain Containing 1 (DBNDD1) gene is located on chr16 :90071278-90085937 at 16q24.3.
Gene Name: Dysbindin Domain Containing 1
Chromosome: CHR16: 90071278 -90085937
Locus: 16q24.3
NAT8L Gene Summary
This gene encodes a single-pass membrane protein, which contains a conserved sequence of the GCN5 or NAT superfamily of N-acetyltransferases and is a member of the N-acyltransferase (NAT) superfamily. This protein is a neuron-specific protein and is the N-acetylaspartate (NAA) biosynthetic enzyme, catalyzing the NAA synthesis from L-aspartate and acetyl-CoA. NAA is a major storage and transport form of acetyl coenzyme A specific to the nervous system. The gene mutation results in primary NAA deficiency (hypoacetylaspartia). [provided by RefSeq, Dec 2010]
Gene Name: N-acetyltransferase 8 Like
Chromosome: CHR4: 2061238 -2070816
Locus: 4p16.3
Gene Diseases
The NAT8L DBNDD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Glioblastoma Multiforme |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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