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APOBEC3C is a member of the cytidine deaminase gene family. Zusätzlich bieten wir Ihnen APOBEC3C Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal APOBEC3C Primary Antibody für ELISA, WB - ABIN314234
Baumert, Rösler, Malim, von Weizsäcker: Hepatitis B virus DNA is subject to extensive editing by the human deaminase APOBEC3C. in Hepatology (Baltimore, Md.) 2007
Data suggest that heat shock proteins, in particular Hsp90 (zeige HSP90 Antikörper), stimulate APOBEC3 (zeige APOBEC3F Antikörper)-mediated DNA deamination activity toward hepatitis B viral DNA, suggesting a potential physiological role in mutagenesis/carcinogenesis and viral innate immunity; Hsp90 (zeige HSP90 Antikörper) stimulates deamination activity of APOBEC3G (zeige APOBEC3G Antikörper), APOBEC3B (zeige APOBEC3B Antikörper), and APOBEC3C during co-expression in human liver HepG2 cells.
our results suggest that APOBEC3C is in fact involved in protecting hosts from lentiviruses.
Antiviral functions of APOBEC3C against HIV-1 and APOBEC3C binding capacity
These results suggest that functional potential of APOBEC3B (zeige APOBEC3B Antikörper) and APOBEC3C involved in cancer mutagenesis is associated with estrogen receptor (zeige ESR1 Antikörper) status.
High APOBEC3C is associated with the pathogenesis of primary effusion lymphoma.
Expression of APOBEC3A (zeige APOBEC3A Antikörper) or 3C in 293FT cells reduced the infectivity of HPV16 pseudovirions. The reduced infectivity of virions assembled in the presence of APOBEC3A (zeige APOBEC3A Antikörper), but not 3C, was attributed to decreased copy number of the encapsidated reporter plasmid.
APOBEC3 (zeige APOBEC3F Antikörper) deaminases upregulated by IFN-beta (zeige IFNB1 Antikörper) induce E2 hypermutation of HPV16 in cervical keratinocytes.
The mechanism of APOBEC3C (A3C)-mediated LINE-1 inhibition was found to be deaminase independent, required an intact dimerization site and the RNA-binding pocket mutation R122A abolished L1 restriction by A3C.
This study confirmed the association of the APOBEC3 (zeige APOBEC3F Antikörper) deletion with breast cancer risk among women of European ancestry.
a high-resolution crystal structure of APOBEC3C with the HIV-1 viral infectivity factor (Vif (zeige BTG1 Antikörper))-interaction interface.
This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control.
apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3C
, DNA dC->dU-editing enzyme APOBEC-3C
, phorbolin I
, probable DNA dC->dU-editing enzyme APOBEC-3C