Gene-specific Copy Number Variation Probe-ASXL3
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| Catalog: |
CNVFP-ASXL3-01323 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ASXL3). 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: |
ASXL3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ASXL3 genes. This product achieves the purpose of detection by hybridizing with the ASXL3 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 |
Additional Sex Combs Like 3, Transcriptional Regulator |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein containing a plant homeodomain (PHD) zinc finger domain that plays a role in the regulation of gene transcription. The encoded protein has been shown to negatively regulate lipogenesis by binding to and inhibiting the transcriptional activity of two nuclear hormone receptors, oxysterols receptor LXR-alpha (LXRalpha) and thyroid hormone receptor beta (TRbeta). The encoded protein may also inhibit histone deubiquitination. Mutations in this gene have been identified in human patients with Bainbridge-Ropers syndrome, which is characterized by feeding difficulties, developmental delay and other features. [provided by RefSeq, May 2017] |
| Gene Symbol |
ASXL3 |
| Location |
18q12.1 |
| Chromosome |
Chromosome18 |
| Coordinates |
This gene maps to 31158540-31327399 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-ASXL3-01323-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ASXL3-01323-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ASXL3-01323-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ASXL3-01323-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ASXL3-01323-AQ |
467nm |
418nm |
|
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