Gene-specific Copy Number Variation Probe-NALCN
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| Catalog: |
CNVFP-NALCN-13957 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NALCN). 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: |
NALCN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NALCN genes. This product achieves the purpose of detection by hybridizing with the NALCN 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 |
Sodium Leak Channel, Non-selective |
| Gene Summary [Provided by RefSeq] |
This gene encodes a voltage-independent, nonselective cation channel which belongs to a family of voltage-gated sodium and calcium channels that regulates the resting membrane potential and excitability of neurons. This family is expressed throughout the nervous system and conducts a persistent sodium leak current that contributes to tonic neuronal excitability. The encoded protein forms a channelosome complex that includes G-protein-coupled receptors, UNC-79, UNC-80, NCA localization factor-1, and src family tyrosine kinases. Naturally occurring mutations in this gene are associated with infantile neuroaxonal dystrophy, infantile hypotonia with psychomotor retardation and characteristic facies (IHPRF) syndrome, and congenital contractures of the limbs and face with hypotonia and developmental delay (CLIFAHDD) syndrome. A knockout of the orthologous gene in mice results in paralysis with a severely disrupted respiratory rhythm, and lethality within 24 hours after birth. [provided by RefSeq, Apr 2017] |
| Gene Symbol |
NALCN |
| Location |
13q32.3-q33.1 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 101706129-102068813 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-NALCN-13957-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NALCN-13957-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NALCN-13957-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NALCN-13957-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NALCN-13957-AQ |
467nm |
418nm |
|
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