Gene-specific Copy Number Variation Probe-SLC48A1
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Catalog: |
CNVFP-SLC48A1-18756 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC48A1). 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: |
SLC48A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC48A1 genes. This product achieves the purpose of detection by hybridizing with the SLC48A1 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 48 Member 1 |
Gene Summary [Provided by RefSeq] |
The Solute Carrier Family 48 Member 1 (SLC48A1) gene is located on chr12:48166966 -48176536 at 12q13.11. |
Gene Symbol |
SLC48A1 |
Location |
12q13.11 |
Chromosome |
Chromosome12 |
Coordinates |
This gene maps to 48166966-48176536 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-SLC48A1-18756-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC48A1-18756-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC48A1-18756-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC48A1-18756-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC48A1-18756-AQ |
467nm |
418nm |
|
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