Gene-specific Copy Number Variation Probe-PJA1
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| Catalog: |
CNVFP-PJA1-15755 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PJA1). 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: |
PJA1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PJA1 genes. This product achieves the purpose of detection by hybridizing with the PJA1 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 |
Praja Ring Finger Ubiquitin Ligase 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
| Gene Symbol |
PJA1 |
| Location |
Xq13.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 68380580-68385365 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-PJA1-15755-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PJA1-15755-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PJA1-15755-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PJA1-15755-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PJA1-15755-AQ |
467nm |
418nm |
|
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