Gene-specific Copy Number Variation Probe-GRIN2B
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| Catalog: |
CNVFP-GRIN2B-06209 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GRIN2B). 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: |
GRIN2B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GRIN2B genes. This product achieves the purpose of detection by hybridizing with the GRIN2B 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 2B |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the N-methyl-D-aspartate (NMDA) receptor family within the ionotropic glutamate receptor superfamily. The encoded protein is a subunit of the NMDA receptor ion channel which acts as an agonist binding site for glutamate. The NMDA receptors mediate a slow calcium-permeable component of excitatory synaptic transmission in the central nervous system. The NMDA receptors are heterotetramers of seven genetically encoded, differentially expressed subunits including NR1 (GRIN1), NR2 (GRIN2A, GRIN2B, GRIN2C, or GRIN2D) and NR3 (GRIN3A or GRIN3B). The early expression of this gene in development suggests a role in brain development, circuit formation, synaptic plasticity, and cellular migration and differentiation. Naturally occurring mutations within this gene are associated with neurodevelopmental disorders including autism spectrum disorder, attention deficit hyperactivity disorder, epilepsy, and schizophrenia. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
GRIN2B |
| Location |
12p13.1 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 13714409-14133022 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-GRIN2B-06209-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GRIN2B-06209-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GRIN2B-06209-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GRIN2B-06209-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GRIN2B-06209-AQ |
467nm |
418nm |
|
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