Gene-specific Copy Number Variation Probe-PSG9
Add to Cart
Catalog: |
CNVFP-PSG9-16457 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PSG9). 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: |
PSG9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PSG9 genes. This product achieves the purpose of detection by hybridizing with the PSG9 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 |
Pregnancy Specific Beta-1-glycoprotein 9 |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the pregnancy-specific glycoprotein (PSG) family. This protein family and the closely related carcinoembryonic antigen cell adhesion molecule (CEACAM) gene family are both members of the immunoglobulin superfamily, and are organized as a large gene cluster. This protein is thought to inhibit platelet-fibrinogen interactions. Several studies suggest that reduced serum concentrations of PSGs are associated with fetal growth restrictions, while up-regulation of this gene has been observed in colorectal cancers. Several pseudogenes of this gene are found on chromosome 19. Alternative splicing results in multiple transcript variants that encode multiple protein isoforms. [provided by RefSeq, Sep 2014] |
Gene Symbol |
PSG9 |
Location |
19q13.31 |
Chromosome |
Chromosome19 |
Coordinates |
This gene maps to 43757434-43773682 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-PSG9-16457-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PSG9-16457-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PSG9-16457-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PSG9-16457-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PSG9-16457-AQ |
467nm |
418nm |
|
Other Products