Gene-specific Copy Number Variation Probe-GRIN2C
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| Catalog: |
CNVFP-GRIN2C-06207 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GRIN2C). 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: |
GRIN2C Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GRIN2C genes. This product achieves the purpose of detection by hybridizing with the GRIN2C 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 NMDA Type Subunit 2C |
| Gene Summary [Provided by RefSeq] |
This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptor, which is a subtype of ionotropic glutamate receptor. NMDA receptors are found in the central nervous system, are permeable to cations and have an important role in physiological processes such as learning, memory, and synaptic development. The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A-D), forming a channel that is permeable to calcium, potassium, and sodium, and whose properties are determined by subunit composition. Alterations in the subunit composition of the receptor are associated with pathophysiological conditions such as Parkinson's disease, Alzheimer's disease, depression, and schizophrenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2013] |
| Gene Symbol |
GRIN2C |
| Location |
17q25.1 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 72838167-72856007 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-GRIN2C-06207-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GRIN2C-06207-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GRIN2C-06207-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GRIN2C-06207-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GRIN2C-06207-AQ |
467nm |
418nm |
|
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