PSMB3 (NM_002795) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC201296L3V
- LentiORF®
Lenti ORF particles, PSMB3 (Myc-DDK tagged) - Human proteasome (prosome, macropain) subunit, beta type, 3 (PSMB3), 200ul, >10^7 TU/mL
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CNY 7,410.00
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Specifications
Product Data | |
Product Name | PSMB3 (NM_002795) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | HC10-II |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_002795 |
ORF Size | 615 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC201296).
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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_002795.2 |
RefSeq Size | 809 bp |
RefSeq ORF | 618 bp |
Locus ID | 5691 |
Domains | proteasome |
Protein Families | Druggable Genome, Protease |
Protein Pathways | Proteasome |
MW | 22.9 kDa |
Gene Summary | The proteasome is a multicatalytic proteinase complex with a highly ordered ring-shaped 20S core structure. The core structure is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 alpha subunits and 2 rings are composed of 7 beta subunits. Proteasomes are distributed throughout eukaryotic cells at a high concentration and cleave peptides in an ATP/ubiquitin-dependent process in a non-lysosomal pathway. An essential function of a modified proteasome, the immunoproteasome, is the processing of class I MHC peptides. This gene encodes a member of the proteasome B-type family, also known as the T1B family, that is a 20S core beta subunit. The 26 S proteasome may be involved in trinucleotide repeat expansion, a phenomenon which is associated with many hereditary neurological diseases. Pseudogenes have been identified on chromosomes 2 and 12. Alternative splicing results in multiple transcript variants [provided by RefSeq, Sep 2013] |
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