Gene-specific Copy Number Variation Probe-SLC26A5
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| Catalog: |
CNVFP-SLC26A5-18517 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC26A5). 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: |
SLC26A5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC26A5 genes. This product achieves the purpose of detection by hybridizing with the SLC26A5 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 26 Member 5 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009] |
| Gene Symbol |
SLC26A5 |
| Location |
7q22.1 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 102993176-103086624 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-SLC26A5-18517-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC26A5-18517-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC26A5-18517-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC26A5-18517-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC26A5-18517-AQ |
467nm |
418nm |
|
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