Gene-specific Copy Number Variation Probe-BAD
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| Catalog: |
CNVFP-BAD-01491 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BAD). 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: |
BAD Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BAD genes. This product achieves the purpose of detection by hybridizing with the BAD 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 |
BCL2 Associated Agonist Of Cell Death |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the BCL-2 family. BCL-2 family members are known to be regulators of programmed cell death. This protein positively regulates cell apoptosis by forming heterodimers with BCL-xL and BCL-2, and reversing their death repressor activity. Proapoptotic activity of this protein is regulated through its phosphorylation. Protein kinases AKT and MAP kinase, as well as protein phosphatase calcineurin were found to be involved in the regulation of this protein. Alternative splicing of this gene results in two transcript variants which encode the same isoform. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
BAD |
| Location |
11q13.1 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 64037299-64052176 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-BAD-01491-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BAD-01491-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BAD-01491-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BAD-01491-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BAD-01491-AQ |
467nm |
418nm |
|
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