Gene-specific Copy Number Variation Probe-ARHGAP11A
Add to Cart
| Catalog: |
CNVFP-ARHGAP11A-00802 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ARHGAP11A). 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: |
ARHGAP11A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ARHGAP11A genes. This product achieves the purpose of detection by hybridizing with the ARHGAP11A 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 |
Rho GTPase Activating Protein 11A |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the Rho GTPase activating protein family. In response to DNA damage, the encoded protein interacts with the p53 tumor suppressor protein and stimulates its tetramerization, which results in cell-cycle arrest and apoptosis. A chromosomal deletion that includes this gene is one cause of Prader-Willi syndrome, and an intronic variant of this gene may be associated with sleep duration in children. This gene is highly expressed in colon cancers and in a human basal-like breast cancer cell line. [provided by RefSeq, Sep 2016] |
| Gene Symbol |
ARHGAP11A |
| Location |
15q13.3 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 32907690-32931868 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-ARHGAP11A-00802-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ARHGAP11A-00802-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ARHGAP11A-00802-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ARHGAP11A-00802-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ARHGAP11A-00802-AQ |
467nm |
418nm |
|
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