Gene-specific Copy Number Variation Probe-RAD50
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| Catalog: |
CNVFP-RAD50-17102 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RAD50). 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: |
RAD50 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RAD50 genes. This product achieves the purpose of detection by hybridizing with the RAD50 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 |
RAD50 Double Strand Break Repair Protein |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Rad50, a protein involved in DNA double-strand break repair. This protein forms a complex with MRE11 and NBS1. The protein complex binds to DNA and displays numerous enzymatic activities that are required for nonhomologous joining of DNA ends. This protein, cooperating with its partners, is important for DNA double-strand break repair, cell cycle checkpoint activation, telomere maintenance, and meiotic recombination. Knockout studies of the mouse homolog suggest this gene is essential for cell growth and viability. Mutations in this gene are the cause of Nijmegen breakage syndrome-like disorder.[provided by RefSeq, Apr 2010] |
| Gene Symbol |
RAD50 |
| Location |
5q31.1 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 131892615-131980313 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-RAD50-17102-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RAD50-17102-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RAD50-17102-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RAD50-17102-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RAD50-17102-AQ |
467nm |
418nm |
|
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