Gene-specific Copy Number Variation Probe-SLC5A7
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Catalog: |
CNVFP-SLC5A7-18727 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC5A7). 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: |
SLC5A7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC5A7 genes. This product achieves the purpose of detection by hybridizing with the SLC5A7 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 5 Member 7 |
Gene Summary [Provided by RefSeq] |
This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015] |
Gene Symbol |
SLC5A7 |
Location |
2q12.3 |
Chromosome |
Chromosome2 |
Coordinates |
This gene maps to 108602994-108630443 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-SLC5A7-18727-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC5A7-18727-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC5A7-18727-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC5A7-18727-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC5A7-18727-AQ |
467nm |
418nm |
|
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