Gene-specific Copy Number Variation Probe-APBB1
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| Catalog: |
CNVFP-APBB1-00750 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (APBB1). 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: |
APBB1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to APBB1 genes. This product achieves the purpose of detection by hybridizing with the APBB1 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 |
Amyloid Beta Precursor Protein Binding Family B Member 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer's disease amyloid precursor protein (APP), transcription factor CP2/LSF/LBP1 and the low-density lipoprotein receptor-related protein. APP functions as a cytosolic anchoring site that can prevent the gene product's nuclear translocation. This encoded protein could play an important role in the pathogenesis of Alzheimer's disease. It is thought to regulate transcription. Also it is observed to block cell cycle progression by downregulating thymidylate synthase expression. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Mar 2012] |
| Gene Symbol |
APBB1 |
| Location |
11p15.4 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 6416354-6440644 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-APBB1-00750-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-APBB1-00750-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-APBB1-00750-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-APBB1-00750-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-APBB1-00750-AQ |
467nm |
418nm |
|
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