Gene-specific Copy Number Variation Probe-TP63
Add to Cart
| Catalog: |
CNVFP-TP63-21491 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TP63). 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: |
TP63 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TP63 genes. This product achieves the purpose of detection by hybridizing with the TP63 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 |
Tumor Protein P63 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the p53 family of transcription factors. The functional domains of p53 family proteins include an N-terminal transactivation domain, a central DNA-binding domain and an oligomerization domain. Alternative splicing of this gene and the use of alternative promoters results in multiple transcript variants encoding different isoforms that vary in their functional properties. These isoforms function during skin development and maintenance, adult stem/progenitor cell regulation, heart development and premature aging. Some isoforms have been found to protect the germline by eliminating oocytes or testicular germ cells that have suffered DNA damage. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrimal-tooth); limb-mammary syndrome; Rap-Hodgkin syndrome (RHS); and orofacial cleft 8. [provided by RefSeq, Aug 2016] |
| Gene Symbol |
TP63 |
| Location |
3q28 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 189349215-189615068 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-TP63-21491-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TP63-21491-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TP63-21491-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TP63-21491-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TP63-21491-AQ |
467nm |
418nm |
|
Other Products
