p16 ARC (ARPC5) (NM_005717) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC212631L3V
- LentiORF®
Lenti ORF particles, ARPC5 (Myc-DDK tagged) - Human actin related protein 2/3 complex, subunit 5, 16kDa (ARPC5), 200ul, >10^7 TU/mL
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CNY 7,410.00
Cited in 1 publication. |
CNY 2,950.00
CNY 1,999.00
CNY 2,700.00
Specifications
Product Data | |
Product Name | p16 ARC (ARPC5) (NM_005717) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | ARC16; dJ127C7.3; p16-Arc |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_005717 |
ORF Size | 453 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC212631).
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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_005717.2 |
RefSeq Size | 2000 bp |
RefSeq ORF | 456 bp |
Locus ID | 10092 |
Domains | p16_Arc |
Protein Pathways | Fc gamma R-mediated phagocytosis, Pathogenic Escherichia coli infection, Regulation of actin cytoskeleton |
MW | 16.1 kDa |
Gene Summary | This gene encodes one of seven subunits of the human Arp2/3 protein complex. The Arp2/3 protein complex has been implicated in the control of actin polymerization in cells and has been conserved through evolution. The exact role of the protein encoded by this gene, the p16 subunit, has yet to be determined. Alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
Citations (1)
The use of this cDNA Clones has been cited in the following citations: |
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Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling
,null,
Nature Communications
,PubMed ID 37349293
[ARPC5]
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