Gene-specific Copy Number Variation Probe-CA8
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| Catalog: |
CNVFP-CA8-01745 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CA8). 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: |
CA8 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CA8 genes. This product achieves the purpose of detection by hybridizing with the CA8 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 |
Carbonic Anhydrase 8 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene was initially named CA-related protein because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i.e., the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. The absence of CA8 gene transcription in the cerebellum of the lurcher mutant in mice with a neurologic defect suggests an important role for this acatalytic form. Mutations in this gene are associated with cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CMARQ3). Polymorphisms in this gene are associated with osteoporosis, and overexpression of this gene in osteosarcoma cells suggests an oncogenic role. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
| Gene Symbol |
CA8 |
| Location |
8q12.1 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 61101422-61193954 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-CA8-01745-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CA8-01745-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CA8-01745-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CA8-01745-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CA8-01745-AQ |
467nm |
418nm |
|
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