Gene-specific Copy Number Variation Probe-SLC52A2
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| Catalog: |
CNVFP-SLC52A2-18677 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC52A2). 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: |
SLC52A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC52A2 genes. This product achieves the purpose of detection by hybridizing with the SLC52A2 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 52 Member 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia. [provided by RefSeq, Jul 2012] |
| Gene Symbol |
SLC52A2 |
| Location |
8q24.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 144358546-144361285 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-SLC52A2-18677-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SLC52A2-18677-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SLC52A2-18677-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SLC52A2-18677-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SLC52A2-18677-AQ |
467nm |
418nm |
|
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