Gene-specific Copy Number Variation Probe-SPRTN
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| Catalog: |
CNVFP-SPRTN-19974 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPRTN). 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: |
SPRTN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPRTN genes. This product achieves the purpose of detection by hybridizing with the SPRTN 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 |
SprT-like N-terminal Domain |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015] |
| Gene Symbol |
SPRTN |
| Location |
1q42.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 231337935-231355028 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-SPRTN-19974-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SPRTN-19974-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SPRTN-19974-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SPRTN-19974-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SPRTN-19974-AQ |
467nm |
418nm |
|
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