CNOT7 (NM_013354) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC209293L4V
- LentiORF®
Lenti ORF particles, CNOT7 (mGFP-tagged) - Human CCR4-NOT transcription complex, subunit 7 (CNOT7), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 9,120.00
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Specifications
Product Data | |
Product Name | CNOT7 (NM_013354) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CAF-1; CAF1; Caf1a; hCAF-1 |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_013354 |
ORF Size | 855 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC209293).
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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_013354.5 |
RefSeq Size | 2646 bp |
RefSeq ORF | 858 bp |
Locus ID | 29883 |
Domains | CAF1 |
Protein Families | Transcription Factors |
Protein Pathways | RNA degradation |
MW | 32.7 kDa |
Gene Summary | The protein encoded by this gene binds to an anti-proliferative protein, B-cell translocation protein 1, which negatively regulates cell proliferation. Binding of the two proteins, which is driven by phosphorylation of the anti-proliferative protein, causes signaling events in cell division that lead to changes in cell proliferation associated with cell-cell contact. The encoded protein downregulates the innate immune response and therefore provides a therapeutic target for enhancing its antimicrobial activity against foreign agents. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1 and X. [provided by RefSeq, Apr 2016] |
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