Gene-specific Copy Number Variation Probe-SLC12A3
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Catalog: |
CNVFP-SLC12A3-18650 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC12A3). 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: |
SLC12A3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC12A3 genes. This product achieves the purpose of detection by hybridizing with the SLC12A3 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 12 Member 3 |
Gene Summary [Provided by RefSeq] |
This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Gene Symbol |
SLC12A3 |
Location |
16q13 |
Chromosome |
Chromosome16 |
Coordinates |
This gene maps to 56899118-56949762 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-SLC12A3-18650-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC12A3-18650-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC12A3-18650-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC12A3-18650-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC12A3-18650-AQ |
467nm |
418nm |
|
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