Gene-specific Copy Number Variation Probe-GRIN2A
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| Catalog: |
CNVFP-GRIN2A-06211 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GRIN2A). 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: |
GRIN2A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GRIN2A genes. This product achieves the purpose of detection by hybridizing with the GRIN2A 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 2A |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the glutamate-gated ion channel protein family. The encoded protein is an N-methyl-D-aspartate (NMDA) receptor subunit. NMDA receptors are both ligand-gated and voltage-dependent, and are involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. These receptors are permeable to calcium ions, and activation results in a calcium influx into post-synaptic cells, which results in the activation of several signaling cascades. Disruption of this gene is associated with focal epilepsy and speech disorder with or without cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014] |
| Gene Symbol |
GRIN2A |
| Location |
16p13.2 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 9847264-10276611 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-GRIN2A-06211-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GRIN2A-06211-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GRIN2A-06211-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GRIN2A-06211-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GRIN2A-06211-AQ |
467nm |
418nm |
|
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