Gene-specific Copy Number Variation Probe-GFM2
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| Catalog: |
CNVFP-GFM2-05977 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GFM2). 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: |
GFM2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GFM2 genes. This product achieves the purpose of detection by hybridizing with the GFM2 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 |
G Elongation Factor Mitochondrial 2 |
| Gene Summary [Provided by RefSeq] |
Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors, which is a GTPase that plays a role at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA . Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
GFM2 |
| Location |
5q13.3 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 74017030-74063042 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-GFM2-05977-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GFM2-05977-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GFM2-05977-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GFM2-05977-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GFM2-05977-AQ |
467nm |
418nm |
|
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