Gene-specific Copy Number Variation Probe-NRG2
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| Catalog: |
CNVFP-NRG2-14412 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NRG2). 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: |
NRG2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NRG2 genes. This product achieves the purpose of detection by hybridizing with the NRG2 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 |
Neuregulin 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a novel member of the neuregulin family of growth and differentiation factors. Through interaction with the ERBB family of receptors, this protein induces the growth and differentiation of epithelial, neuronal, glial, and other types of cells. The gene consists of 12 exons and the genomic structure is similar to that of neuregulin 1, another member of the neuregulin family of ligands. The products of these genes mediate distinct biological processes by acting at different sites in tissues and eliciting different biological responses in cells. This gene is located close to the region for demyelinating Charcot-Marie-Tooth disease locus, but is not responsible for this disease. Alternative transcript variants encoding distinct isoforms have been described. [provided by RefSeq, May 2010] |
| Gene Symbol |
NRG2 |
| Location |
5q31.2 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 139226363-139422884 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-NRG2-14412-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NRG2-14412-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NRG2-14412-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NRG2-14412-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NRG2-14412-AQ |
467nm |
418nm |
|
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