Gene-specific Copy Number Variation Probe-GP9
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| Catalog: |
CNVFP-GP9-06027 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GP9). 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: |
GP9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GP9 genes. This product achieves the purpose of detection by hybridizing with the GP9 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 |
Glycoprotein IX Platelet |
| Gene Summary [Provided by RefSeq] |
This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency. [provided by RefSeq, Oct 2008] |
| Gene Symbol |
GP9 |
| Location |
3q21.3 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 128779644-128781253 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-GP9-06027-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GP9-06027-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GP9-06027-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GP9-06027-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GP9-06027-AQ |
467nm |
418nm |
|
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