Gene-specific Copy Number Variation Probe-SLC35A4
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Catalog: |
CNVFP-SLC35A4-18795 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC35A4). 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: |
SLC35A4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC35A4 genes. This product achieves the purpose of detection by hybridizing with the SLC35A4 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 35 Member A4 |
Gene Summary [Provided by RefSeq] |
The Solute Carrier Family 35 Member A4 (SLC35A4) gene is located on chr5:139944419 -139948683 at 5q31.3. |
Gene Symbol |
SLC35A4 |
Location |
5q31.3 |
Chromosome |
Chromosome5 |
Coordinates |
This gene maps to 139944419-139948683 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-SLC35A4-18795-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC35A4-18795-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC35A4-18795-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC35A4-18795-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC35A4-18795-AQ |
467nm |
418nm |
|
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