Gene-specific Copy Number Variation Probe-APLP2
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| Catalog: |
CNVFP-APLP2-00897 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (APLP2). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
APLP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to APLP2 genes. This product achieves the purpose of detection by hybridizing with the APLP2 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Amyloid Beta Precursor Like Protein 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes amyloid precursor- like protein 2 (APLP2), which is a member of the APP (amyloid precursor protein) family including APP, APLP1 and APLP2. This protein is ubiquitously expressed. It contains heparin-, copper- and zinc- binding domains at the N-terminus, BPTI/Kunitz inhibitor and E2 domains in the middle region, and transmembrane and intracellular domains at the C-terminus. This protein interacts with major histocompatibility complex (MHC) class I molecules. The synergy of this protein and the APP is required to mediate neuromuscular transmission, spatial learning and synaptic plasticity. This protein has been implicated in the pathogenesis of Alzheimer's disease. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Aug 2011] |
| Gene Symbol |
APLP2 |
| Location |
11q24.3 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 129939715-130014706 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-APLP2-00897-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-APLP2-00897-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-APLP2-00897-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-APLP2-00897-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-APLP2-00897-AQ |
467nm |
418nm |
|
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