Gene-specific Copy Number Variation Probe-RNF111
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Catalog: |
CNVFP-RNF111-17309 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RNF111). 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: |
RNF111 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RNF111 genes. This product achieves the purpose of detection by hybridizing with the RNF111 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 |
Ring Finger Protein 111 |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a nuclear RING-domain containing E3 ubiquitin ligase. This protein interacts with the transforming growth factor (TGF) -beta/NODAL signaling pathway by promoting the ubiquitination and proteosomal degradation of negative regulators, like SMAD proteins, and thereby enhances TGF-beta target-gene transcription. As a modulator of the nodal signaling cascade, this gene plays a critical role in the induction of mesoderm during embryonic development. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012] |
Gene Symbol |
RNF111 |
Location |
15q22.1-q22.2 |
Chromosome |
Chromosome15 |
Coordinates |
This gene maps to 59279864-59389253 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-RNF111-17309-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-RNF111-17309-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-RNF111-17309-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-RNF111-17309-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-RNF111-17309-AQ |
467nm |
418nm |
|
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