Gene-specific Copy Number Variation Probe-TGFBR2
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| Catalog: |
CNVFP-TGFBR2-20538 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TGFBR2). 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: |
TGFBR2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TGFBR2 genes. This product achieves the purpose of detection by hybridizing with the TGFBR2 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 |
Transforming Growth Factor Beta Receptor 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a transmembrane protein that has a protein kinase domain, forms a heterodimeric complex with TGF-beta receptor type-1, and binds TGF-beta. This receptor/ligand complex phosphorylates proteins, which then enter the nucleus and regulate the transcription of genes related to cell proliferation, cell cycle arrest, wound healing, immunosuppression, and tumorigenesis. Mutations in this gene have been associated with Marfan Syndrome, Loeys-Deitz Aortic Aneurysm Syndrome, and the development of various types of tumors. Alternatively spliced transcript variants encoding different isoforms have been characterized. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
TGFBR2 |
| Location |
3p24.1 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 30647993-30735633 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-TGFBR2-20538-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TGFBR2-20538-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TGFBR2-20538-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TGFBR2-20538-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TGFBR2-20538-AQ |
467nm |
418nm |
|
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