NAT8L Break Apart FISH Probe
Empire Genomics’ NAT8L Break Apart FISH Probe is designed to flank the NAT8L gene and is typically used for detecting NAT8L rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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 |
|---|---|---|---|---|
| NAT8LBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-GROR | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| NAT8LBA-20-REGR | 20 (40 μL) | 200 μL |
|
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 Details
Gene Symbol: NAT8L
Gene Name: N-acetyltransferase 8 Like
Chromosome: CHR4: 2061238-2070816
Locus: 4p16.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: NAT8L FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: NAT8L-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping