Gene-specific Copy Number Variation Probe-PSAP
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| Catalog: |
CNVFP-PSAP-16514 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PSAP). 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: |
PSAP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PSAP genes. This product achieves the purpose of detection by hybridizing with the PSAP 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 |
Prosaposin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a highly conserved preproprotein that is proteolytically processed to generate four main cleavage products including saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016] |
| Gene Symbol |
PSAP |
| Location |
10q22.1 |
| Chromosome |
Chromosome10 |
| Coordinates |
This gene maps to 73576054-73611082 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-PSAP-16514-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PSAP-16514-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PSAP-16514-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PSAP-16514-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PSAP-16514-AQ |
467nm |
418nm |
|
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