Gene-specific Copy Number Variation Probe-GOLGA6A
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| Catalog: |
CNVFP-GOLGA6A-06093 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GOLGA6A). 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: |
GOLGA6A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GOLGA6A genes. This product achieves the purpose of detection by hybridizing with the GOLGA6A 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 |
Golgin A6 Family Member A |
| Gene Summary [Provided by RefSeq] |
The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The protein encoded by this gene is a member of the golgin family of proteins, whose members localize to the Golgi. This gene is found in a large, low copy repeat sequence or duplicon that is found in multiple copies, that are greather than 90% similar, on chromosome 15. Duplicons are associated with deletions, inversions and other chromosome rearrangements that underlie genomic disease. The protein encoded by this gene is thought to be a functional golgin protein while the majority of the related copies of this gene are thought to be transcribed pseudogenes. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
GOLGA6A |
| Location |
15q24.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 74362197-74374891 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-GOLGA6A-06093-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GOLGA6A-06093-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GOLGA6A-06093-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GOLGA6A-06093-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GOLGA6A-06093-AQ |
467nm |
418nm |
|
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