Gene-specific Copy Number Variation Probe-SIPA1L3
Add to Cart
| Catalog: |
CNVFP-SIPA1L3-18377 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SIPA1L3). 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: |
SIPA1L3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SIPA1L3 genes. This product achieves the purpose of detection by hybridizing with the SIPA1L3 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 |
Signal Induced Proliferation Associated 1 Like 3 |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the signal induced proliferation associated 1 family of genes, which encode GTPase-activating proteins specific for the GTP-binding protein Rap1. Rap1 has been implicated in regulation of cell adhesion, cell polarity, and organization of the cytoskeleton. Like other members of the family, the protein encoded by this gene contains RapGAP and PDZ domains. In addition, this protein contains a C-terminal leucine zipper domain. This gene is proposed to function in epithelial cell morphogenesis and establishment or maintenance of polarity. Consistently, expression of the protein in cell culture showed localization to cell-cell borders in apical regions, and downregulation of the gene in 3D Caco2 cell culture resulted in abnormal cell polarity and morphogenesis. Allelic variants of this gene have been associated with congenital cataracts in humans. [provided by RefSeq, Feb 2016] |
| Gene Symbol |
SIPA1L3 |
| Location |
19q13.13-q13.2 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 38397867-38699008 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-SIPA1L3-18377-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SIPA1L3-18377-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SIPA1L3-18377-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SIPA1L3-18377-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SIPA1L3-18377-AQ |
467nm |
418nm |
|
Other Products
