Gene-specific Copy Number Variation Probe-GP1BA
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| Catalog: |
CNVFP-GP1BA-06033 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GP1BA). 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: |
GP1BA Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GP1BA genes. This product achieves the purpose of detection by hybridizing with the GP1BA 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 Ib Platelet Alpha Subunit |
| Gene Summary [Provided by RefSeq] |
Glycoprotein Ib (GP Ib) is a platelet surface membrane glycoprotein composed of a heterodimer, an alpha chain and a beta chain, that is linked by disulfide bonds. The Gp Ib functions as a receptor for von Willebrand factor (VWF). The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX and platelet glycoprotein V. The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury, and also initiates signaling events within the platelet that lead to enhanced platelet activation, thrombosis, and hemostasis. This gene encodes the alpha subunit. Mutations in this gene result in Bernard-Soulier syndromes and platelet-type von Willebrand disease. The coding region of this gene is known to contain a polymophic variable number tandem repeat (VNTR) domain that is associated with susceptibility to nonarteritic anterior ischemic optic neuropathy. [provided by RefSeq, Oct 2013] |
| Gene Symbol |
GP1BA |
| Location |
17p13.2 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 4835591-4838325 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-GP1BA-06033-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GP1BA-06033-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GP1BA-06033-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GP1BA-06033-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GP1BA-06033-AQ |
467nm |
418nm |
|
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