Gene-specific Copy Number Variation Probe-CTNNB1
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| Catalog: |
CNVFP-CTNNB1-03493 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CTNNB1). 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: |
CTNNB1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CTNNB1 genes. This product achieves the purpose of detection by hybridizing with the CTNNB1 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 |
Catenin Beta 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (AJs). AJs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. The encoded protein also anchors the actin cytoskeleton and may be responsible for transmitting the contact inhibition signal that causes cells to stop dividing once the epithelial sheet is complete. Finally, this protein binds to the product of the APC gene, which is mutated in adenomatous polyposis of the colon. Mutations in this gene are a cause of colorectal cancer (CRC), pilomatrixoma (PTR), medulloblastoma (MDB), and ovarian cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016] |
| Gene Symbol |
CTNNB1 |
| Location |
3p22.1 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 41240941-41281939 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-CTNNB1-03493-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CTNNB1-03493-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CTNNB1-03493-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CTNNB1-03493-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CTNNB1-03493-AQ |
467nm |
418nm |
|
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