Gene-specific Copy Number Variation Probe-SLC12A1
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| Catalog: |
CNVFP-SLC12A1-18655 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC12A1). 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: |
SLC12A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC12A1 genes. This product achieves the purpose of detection by hybridizing with the SLC12A1 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 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a kidney-specific sodium-potassium-chloride cotransporter that is expressed on the luminal membrane of renal epithelial cells of the thick ascending limb of Henle's loop and the macula densa. It plays a key role in concentrating urine and accounts for most of the NaCl resorption. It is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their biological validity in humans has not been experimentally proven.[provided by RefSeq, May 2010] |
| Gene Symbol |
SLC12A1 |
| Location |
15q21.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 48498497-48596275 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-SLC12A1-18655-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC12A1-18655-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC12A1-18655-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC12A1-18655-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC12A1-18655-AQ |
467nm |
418nm |
|
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