Gene-specific Copy Number Variation Probe-SLC16A2
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| Catalog: |
CNVFP-SLC16A2-18628 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC16A2). 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: |
SLC16A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC16A2 genes. This product achieves the purpose of detection by hybridizing with the SLC16A2 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 16 Member 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012] |
| Gene Symbol |
SLC16A2 |
| Location |
Xq13.2 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 73641084-73753752 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-SLC16A2-18628-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC16A2-18628-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC16A2-18628-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC16A2-18628-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC16A2-18628-AQ |
467nm |
418nm |
|
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