Gene-specific Copy Number Variation Probe-RAD51
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| Catalog: |
CNVFP-RAD51-17101 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RAD51). 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: |
RAD51 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RAD51 genes. This product achieves the purpose of detection by hybridizing with the RAD51 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 |
RAD51 Recombinase |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51, and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with the ssDNA-binding protein RPA and RAD52, and it is thought to play roles in homologous pairing and strand transfer of DNA. This protein is also found to interact with BRCA1 and BRCA2, which may be important for the cellular response to DNA damage. BRCA2 is shown to regulate both the intracellular localization and DNA-binding ability of this protein. Loss of these controls following BRCA2 inactivation may be a key event leading to genomic instability and tumorigenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009] |
| Gene Symbol |
RAD51 |
| Location |
15q15.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 40987326-41024356 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-RAD51-17101-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RAD51-17101-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RAD51-17101-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RAD51-17101-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RAD51-17101-AQ |
467nm |
418nm |
|
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