Gene-specific Copy Number Variation Probe-SLC7A9
Add to Cart
| Catalog: |
CNVFP-SLC7A9-18713 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC7A9). 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: |
SLC7A9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC7A9 genes. This product achieves the purpose of detection by hybridizing with the SLC7A9 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 7 Member 9 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq, Jul 2011] |
| Gene Symbol |
SLC7A9 |
| Location |
19q13.11 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 33321418-33360683 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-SLC7A9-18713-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC7A9-18713-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC7A9-18713-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC7A9-18713-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC7A9-18713-AQ |
467nm |
418nm |
|
Other Products
