Gene-specific Copy Number Variation Probe-GNB3
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| Catalog: |
CNVFP-GNB3-06090 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GNB3). 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: |
GNB3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GNB3 genes. This product achieves the purpose of detection by hybridizing with the GNB3 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 |
G Protein Subunit Beta 3 |
| Gene Summary [Provided by RefSeq] |
Heterotrimeric guanine nucleotide-binding proteins (G proteins), which integrate signals between receptors and effector proteins, are composed of an alpha, a beta, and a gamma subunit. These subunits are encoded by families of related genes. This gene encodes a beta subunit which belongs to the WD repeat G protein beta family. Beta subunits are important regulators of alpha subunits, as well as of certain signal transduction receptors and effectors. A single-nucleotide polymorphism (C825T) in this gene is associated with essential hypertension and obesity. This polymorphism is also associated with the occurrence of the splice variant GNB3-s, which appears to have increased activity. GNB3-s is an example of alternative splicing caused by a nucleotide change outside of the splice donor and acceptor sites. Alternative splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Jul 2014] |
| Gene Symbol |
GNB3 |
| Location |
12p13.31 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 6949374-6956557 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-GNB3-06090-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GNB3-06090-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GNB3-06090-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GNB3-06090-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GNB3-06090-AQ |
467nm |
418nm |
|
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