Gene-specific Copy Number Variation Probe-BAIAP2
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| Catalog: |
CNVFP-BAIAP2-01481 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BAIAP2). 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: |
BAIAP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BAIAP2 genes. This product achieves the purpose of detection by hybridizing with the BAIAP2 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 |
BAI1 Associated Protein 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene has been identified as a brain-specific angiogenesis inhibitor (BAI1)-binding protein. This adaptor protein links membrane bound G-proteins to cytoplasmic effector proteins. This protein functions as an insulin receptor tyrosine kinase substrate and suggests a role for insulin in the central nervous system. It also associates with a downstream effector of Rho small G proteins, which is associated with the formation of stress fibers and cytokinesis. This protein is involved in lamellipodia and filopodia formation in motile cells and may affect neuronal growth-cone guidance. This protein has also been identified as interacting with the dentatorubral-pallidoluysian atrophy gene, which is associated with an autosomal dominant neurodegenerative disease. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Jan 2009] |
| Gene Symbol |
BAIAP2 |
| Location |
17q25.3 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 79008946-79091232 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-BAIAP2-01481-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BAIAP2-01481-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BAIAP2-01481-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BAIAP2-01481-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BAIAP2-01481-AQ |
467nm |
418nm |
|
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