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p63 (TP63) (NM_003722) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC208013L4V
- LentiORF®
-
Lenti ORF particles, TP63 (mGFP-tagged) - Human tumor protein p63 (TP63), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
| Product Data | |
| Product Name | p63 (TP63) (NM_003722) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | AIS; B(p51A); B(p51B); EEC3; KET; LMS; NBP; OFC8; p40; p51; p53CP; p63; p73H; p73L; RHS; SHFM4; TP53CP; TP53L; TP73L |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_003722 |
| ORF Size | 2040 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC208013).
|
| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_003722.3 |
| RefSeq Size | 4927 bp |
| RefSeq ORF | 2043 bp |
| Locus ID | 8626 |
| Domains | SAM, P53 |
| Protein Families | Druggable Genome, Transcription Factors |
| MW | 76.8 kDa |
| Gene Summary | 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] |
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