Gene-specific Copy Number Variation Probe-GEMIN2
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| Catalog: |
CNVFP-GEMIN2-05990 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GEMIN2). 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: |
GEMIN2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GEMIN2 genes. This product achieves the purpose of detection by hybridizing with the GEMIN2 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 |
Gem Nuclear Organelle Associated Protein 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of the proteins found in the SMN complex, which consists of several gemin proteins and the protein known as the survival of motor neuron protein. The SMN complex is localized to a subnuclear compartment called gems (gemini of coiled bodies) and is required for assembly of spliceosomal snRNPs and for pre-mRNA splicing. This protein interacts directly with the survival of motor neuron protein and it is required for formation of the SMN complex. A knockout mouse targeting the mouse homolog of this gene exhibited disrupted snRNP assembly and motor neuron degeneration. [provided by RefSeq, Aug 2011] |
| Gene Symbol |
GEMIN2 |
| Location |
14q21.1 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 39583487-39606177 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-GEMIN2-05990-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GEMIN2-05990-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GEMIN2-05990-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GEMIN2-05990-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GEMIN2-05990-AQ |
467nm |
418nm |
|
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