Gene-specific Copy Number Variation Probe-SLC25A19
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Catalog: |
CNVFP-SLC25A19-18556 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SLC25A19). 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: |
SLC25A19 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SLC25A19 genes. This product achieves the purpose of detection by hybridizing with the SLC25A19 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 19 |
Gene Summary [Provided by RefSeq] |
This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria, further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier, which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly, Amish type, a metabolic disease that results in severe congenital microcephaly, severe 2-ketoglutaric aciduria, and death within the first year. Multiple alternatively spliced variants, encoding the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008] |
Gene Symbol |
SLC25A19 |
Location |
17q25.1 |
Chromosome |
Chromosome17 |
Coordinates |
This gene maps to 73269060-73285530 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-SLC25A19-18556-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SLC25A19-18556-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SLC25A19-18556-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SLC25A19-18556-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SLC25A19-18556-AQ |
467nm |
418nm |
|
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