Gene-specific Copy Number Variation Probe-SURF1
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Catalog: |
CNVFP-SURF1-20337 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SURF1). 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: |
SURF1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SURF1 genes. This product achieves the purpose of detection by hybridizing with the SURF1 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 |
SURF1, Cytochrome C Oxidase Assembly Factor |
Gene Summary [Provided by RefSeq] |
This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. [provided by RefSeq, Jul 2008] |
Gene Symbol |
SURF1 |
Location |
9q34.2 |
Chromosome |
Chromosome9 |
Coordinates |
This gene maps to 136218665-136223361 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-SURF1-20337-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SURF1-20337-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SURF1-20337-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SURF1-20337-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SURF1-20337-AQ |
467nm |
418nm |
|
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