Gene-specific Copy Number Variation Probe-PEX12
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| Catalog: |
CNVFP-PEX12-15640 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PEX12). 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: |
PEX12 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PEX12 genes. This product achieves the purpose of detection by hybridizing with the PEX12 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 |
Peroxisomal Biogenesis Factor 12 |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008] |
| Gene Symbol |
PEX12 |
| Location |
17q12 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 33901813-33905656 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-PEX12-15640-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PEX12-15640-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PEX12-15640-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PEX12-15640-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PEX12-15640-AQ |
467nm |
418nm |
|
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