NAP1L4-ATP11B Fusion FISH Probe
The NAP1L4-ATP11B Fusion FISH Probe is used to confirm a fusion of the NAP1L4 and ATP11B genes. The fusion of the NAP1L4 and ATP11B genes has been associated with Prostate Adenocarcinoma. 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 |
|---|---|---|---|---|
| NAP1L4-ATP11B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-RERE | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-REOR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-REGO | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-REGR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-OROR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GORE | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GROR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| NAP1L4-ATP11B-20-AQAQ | 20 (40 μL) | 200 μL |
|
NAP1L4 Gene Summary
This gene encodes a member of the nucleosome assembly protein (NAP) family which can interact with both core and linker histones. It can shuttle between the cytoplasm and nucleus, suggesting a role as a histone chaperone. This gene is one of several located near the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. [provided by RefSeq, Jul 2008]
Gene Name: Nucleosome Assembly Protein 1 Like 4
Chromosome: CHR11: 2965659 -3013607
Locus: 11p15.4
ATP11B Gene Summary
P-type ATPases, such as ATP11B, are phosphorylated in their intermediate state and drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily transports heavy metal ions, such as Cu(2+) or Cd(2+). Another subfamily transports non-heavy metal ions, such as H(+), Na(+), K(+), or Ca(+). A third subfamily transports amphipaths, such as phosphatidylserine.[supplied by OMIM, Feb 2005]
Gene Name: ATPase Phospholipid Transporting 11B (putative)
Chromosome: CHR3: 182511290 -182639421
Locus: 3q26.33
Gene Diseases
The NAP1L4 ATP11B Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|