Gene-specific Copy Number Variation Probe-FKSG29
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| Catalog: |
CNVFP-FKSG29-05432 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FKSG29). 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: |
FKSG29 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FKSG29 genes. This product achieves the purpose of detection by hybridizing with the FKSG29 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 Summary [Provided by RefSeq] |
The (FKSG29) gene is located on chr13:100003673 -100004281 at 13q32.3. |
| Gene Symbol |
FKSG29 |
| Location |
13q32.3 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 100003673-100004281 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-FKSG29-05432-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FKSG29-05432-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FKSG29-05432-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FKSG29-05432-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FKSG29-05432-AQ |
467nm |
418nm |
|
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