Gene-specific Copy Number Variation Probe-PEX7
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| Catalog: |
CNVFP-PEX7-15626 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PEX7). 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: |
PEX7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PEX7 genes. This product achieves the purpose of detection by hybridizing with the PEX7 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 7 |
| Gene Summary [Provided by RefSeq] |
This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one 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 have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008] |
| Gene Symbol |
PEX7 |
| Location |
6q23.3 |
| Chromosome |
Chromosome6 |
| Coordinates |
This gene maps to 137143701-137235072 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-PEX7-15626-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PEX7-15626-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PEX7-15626-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PEX7-15626-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PEX7-15626-AQ |
467nm |
418nm |
|
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