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DPPA4 (NM_018189) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC205999L4V
- LentiORF®
-
Lenti ORF particles, DPPA4 (mGFP-tagged) - Human developmental pluripotency associated 4 (DPPA4), 200ul, >10^7 TU/mL
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CNY 9,120.00
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Specifications
| Product Data | |
| Product Name | DPPA4 (NM_018189) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | 2410091M23Rik |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_018189 |
| ORF Size | 912 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC205999).
|
| 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_018189.2, NP_060659.2 |
| RefSeq Size | 2823 bp |
| RefSeq ORF | 915 bp |
| Locus ID | 55211 |
| MW | 33.5 kDa |
| Gene Summary | This gene encodes a nuclear factor that is involved in the maintenance of pluripotency in stem cells and essential for embryogenesis. The encoded protein has a scaffold-attachment factor A/B, acinus and PIAS (SAP) domain that binds DNA and is thought to modify chromatin. Mice with a homozygous knockout of the orthologous gene die during late embryonic development or within hours after birth. Knockout embryos are normal in size at embryonic day 18.5 but exhibit skeletal and lung tissue abnormalities. This gene, when mutated, is highly expressed in embryonal carcinomas, pluripotent germ cell tumors, and other cancers and is thought to play an important role in tumor progression. Multiple pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017] |
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