Gene-specific Copy Number Variation Probe-PCNT
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| Catalog: |
CNVFP-PCNT-15444 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PCNT). 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: |
PCNT Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PCNT genes. This product achieves the purpose of detection by hybridizing with the PCNT 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 |
Pericentrin |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015] |
| Gene Symbol |
PCNT |
| Location |
21q22.3 |
| Chromosome |
Chromosome21 |
| Coordinates |
This gene maps to 47744035-47865682 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-PCNT-15444-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PCNT-15444-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PCNT-15444-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PCNT-15444-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PCNT-15444-AQ |
467nm |
418nm |
|
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