Gene-specific Copy Number Variation Probe-SLC25A25
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Catalog: |
CNVFP-SLC25A25-18548 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC25A25). 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: |
SLC25A25 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC25A25 genes. This product achieves the purpose of detection by hybridizing with the SLC25A25 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 |
Solute Carrier Family 25 Member 25 |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to the family of calcium-binding mitochondrial carriers, with a characteristic mitochondrial carrier domain at the C-terminus. These proteins are found in the inner membranes of mitochondria, and function as transport proteins. They shuttle metabolites, nucleotides and cofactors through the mitochondrial membrane and thereby connect and/or regulate cytoplasm and matrix functions. This protein may function as an ATP-Mg/Pi carrier that mediates the transport of Mg-ATP in exchange for phosphate, and likely responsible for the net uptake or efflux of adenine nucleotides into or from the mitochondria. Alternatively spliced transcript variants encoding different isoforms with a common C-terminus but variable N-termini have been described for this gene. [provided by RefSeq, Jul 2012] |
Gene Symbol |
SLC25A25 |
Location |
9q34.11 |
Chromosome |
Chromosome9 |
Coordinates |
This gene maps to 130830478-130871524 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-SLC25A25-18548-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC25A25-18548-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC25A25-18548-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC25A25-18548-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC25A25-18548-AQ |
467nm |
418nm |
|
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