Gene-specific Copy Number Variation Probe-PGAP3
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| Catalog: |
CNVFP-PGAP3-15599 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PGAP3). 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: |
PGAP3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PGAP3 genes. This product achieves the purpose of detection by hybridizing with the PGAP3 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 |
Post-GPI Attachment To Proteins 3 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a glycosylphosphatidylinositol (GPI)-specific phospholipase that primarily localizes to the Golgi apparatus. This ubiquitously expressed gene is predicted to encode a seven-transmembrane protein that removes unsaturated fatty acids from the sn-2 position of GPI. The remodeling of the constituent fatty acids on GPI is thought to be important for the proper association between GPI-anchored proteins and lipid rafts. The tethering of proteins to plasma membranes via posttranslational GPI-anchoring is thought to play a role in protein sorting and trafficking. Mutations in this gene cause an autosomal recessive form of neurologic hyperphosphatasia with cognitive disability (HPMRS4). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
PGAP3 |
| Location |
17q12 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 37827374-37844310 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-PGAP3-15599-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PGAP3-15599-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PGAP3-15599-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PGAP3-15599-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PGAP3-15599-AQ |
467nm |
418nm |
|
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