Gene-specific Copy Number Variation Probe-SLC39A14
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| Catalog: |
CNVFP-SLC39A14-18800 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC39A14). 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: |
SLC39A14 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC39A14 genes. This product achieves the purpose of detection by hybridizing with the SLC39A14 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 39 Member 14 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the the SLC39A family of divalent metal transporters that mediates the cellular uptake of manganese, zinc, iron, and cadmium. The encoded protein contains eight transmembrane domains, a histidine-rich motif, and a metalloprotease motif, and is expressed on the plasma membrane and the endocytic vesicle membrane. It is an important transporter of nontransferrin-bound iron and a critical regulator of manganese homeostasis. Naturally occurring mutations in this gene are associated with neurodegeneration with brain iron accumulation and early-onset parkinsonism-dystonia with hypermanganesemia. [provided by RefSeq, May 2017] |
| Gene Symbol |
SLC39A14 |
| Location |
8p21.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 22224761-22291640 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-SLC39A14-18800-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC39A14-18800-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC39A14-18800-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC39A14-18800-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC39A14-18800-AQ |
467nm |
418nm |
|
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