Gene-specific Copy Number Variation Probe-GRID2
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| Catalog: |
CNVFP-GRID2-06218 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GRID2). 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: |
GRID2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GRID2 genes. This product achieves the purpose of detection by hybridizing with the GRID2 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 |
Glutamate Ionotropic Receptor Delta Type Subunit 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the family of ionotropic glutamate receptors which are the predominant excitatory neurotransmitter receptors in the mammalian brain. The encoded protein is a multi-pass membrane protein that is expressed selectively in cerebellar Purkinje cells. A point mutation in the mouse ortholog, associated with the phenotype named 'lurcher', in the heterozygous state leads to ataxia resulting from selective, cell-autonomous apoptosis of cerebellar Purkinje cells during postnatal development. Mice homozygous for this mutation die shortly after birth from massive loss of mid- and hindbrain neurons during late embryogenesis. This protein also plays a role in synapse organization between parallel fibers and Purkinje cells. Alternate splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause cerebellar ataxia in humans. [provided by RefSeq, Apr 2014] |
| Gene Symbol |
GRID2 |
| Location |
4q22.1-q22.2 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 93225549-94693649 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-GRID2-06218-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GRID2-06218-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GRID2-06218-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GRID2-06218-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GRID2-06218-AQ |
467nm |
418nm |
|
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