Gene-specific Copy Number Variation Probe-SLC46A1
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| Catalog: |
CNVFP-SLC46A1-18759 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC46A1). 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: |
SLC46A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC46A1 genes. This product achieves the purpose of detection by hybridizing with the SLC46A1 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 46 Member 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013] |
| Gene Symbol |
SLC46A1 |
| Location |
17q11.2 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 26721660-26733230 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-SLC46A1-18759-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC46A1-18759-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC46A1-18759-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC46A1-18759-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC46A1-18759-AQ |
467nm |
418nm |
|
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