PCNA (NM_002592) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC201741L4V
- LentiORF®
Lenti ORF particles, PCNA (mGFP-tagged) - Human proliferating cell nuclear antigen (PCNA), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,360.00
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CNY 1,999.00
CNY 2,700.00
Specifications
Product Data | |
Product Name | PCNA (NM_002592) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | ATLD2 |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_002592 |
ORF Size | 783 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC201741).
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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_002592.2, NP_002583.1 |
RefSeq Size | 1355 bp |
RefSeq ORF | 786 bp |
Locus ID | 5111 |
Domains | PCNA |
Protein Families | Druggable Genome, Stem cell - Pluripotency |
Protein Pathways | Base excision repair, Cell cycle, DNA replication, Mismatch repair, Nucleotide excision repair |
MW | 28.8 kDa |
Gene Summary | The protein encoded by this gene is found in the nucleus and is a cofactor of DNA polymerase delta. The encoded protein acts as a homotrimer and helps increase the processivity of leading strand synthesis during DNA replication. In response to DNA damage, this protein is ubiquitinated and is involved in the RAD6-dependent DNA repair pathway. Two transcript variants encoding the same protein have been found for this gene. Pseudogenes of this gene have been described on chromosome 4 and on the X chromosome. [provided by RefSeq, Jul 2008] |
Documents
Product Manuals |
FAQs |
SDS |