Gene-specific Copy Number Variation Probe-PEX19
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| Catalog: |
CNVFP-PEX19-15634 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PEX19). 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: |
PEX19 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PEX19 genes. This product achieves the purpose of detection by hybridizing with the PEX19 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 19 |
| Gene Summary [Provided by RefSeq] |
This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). 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. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some 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), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010] |
| Gene Symbol |
PEX19 |
| Location |
1q23.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 160246598-160254941 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-PEX19-15634-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PEX19-15634-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PEX19-15634-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PEX19-15634-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PEX19-15634-AQ |
467nm |
418nm |
|
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