Gene-specific Copy Number Variation Probe-SLC22A18
Add to Cart
Catalog: |
CNVFP-SLC22A18-18584 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC22A18). 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: |
SLC22A18 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC22A18 genes. This product achieves the purpose of detection by hybridizing with the SLC22A18 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 |
Solute Carrier Family 22 Member 18 |
Gene Summary [Provided by RefSeq] |
This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015] |
Gene Symbol |
SLC22A18 |
Location |
11p15.4 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 2920950-2946476 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-SLC22A18-18584-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC22A18-18584-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC22A18-18584-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC22A18-18584-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC22A18-18584-AQ |
467nm |
418nm |
|
Other Products