Gene-specific Copy Number Variation Probe-RAD23B
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Catalog: |
CNVFP-RAD23B-17104 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RAD23B). 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: |
RAD23B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RAD23B genes. This product achieves the purpose of detection by hybridizing with the RAD23B 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 |
RAD23 Homolog B, Nucleotide Excision Repair Protein |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is one of two human homologs of Saccharomyces cerevisiae Rad23, a protein involved in the nucleotide excision repair (NER). This protein was found to be a component of the protein complex that specifically complements the NER defect of xeroderma pigmentosum group C (XP-c) cell extracts in vitro. This protein was also shown to interact with, and elevate the nucleotide excision activity of 3-methyladenine-DNA glycosylase (MPG), which suggested a role in DNA damage recognition in base excision repair. This protein contains an N-terminal ubiquitin-like domain, which was reported to interact with 26S proteasome, and thus this protein may be involved in the ubiquitin mediated proteolytic pathway in cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Sep 2011] |
Gene Symbol |
RAD23B |
Location |
9q31.2 |
Chromosome |
Chromosome9 |
Coordinates |
This gene maps to 110045543-110094470 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-RAD23B-17104-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-RAD23B-17104-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-RAD23B-17104-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-RAD23B-17104-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-RAD23B-17104-AQ |
467nm |
418nm |
|
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