Gene-specific Copy Number Variation Probe-GPC3
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Catalog: |
CNVFP-GPC3-06321 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GPC3). 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: |
GPC3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GPC3 genes. This product achieves the purpose of detection by hybridizing with the GPC3 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 |
Glypican 3 |
Gene Summary [Provided by RefSeq] |
Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009] |
Gene Symbol |
GPC3 |
Location |
Xq26.2 |
Chromosome |
ChromosomeX |
Coordinates |
This gene maps to 132669775-133119673 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-GPC3-06321-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-GPC3-06321-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-GPC3-06321-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-GPC3-06321-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-GPC3-06321-AQ |
467nm |
418nm |
|
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