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APOBEC3C is a member of the cytidine deaminase gene family.
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Human Polyclonal APOBEC3C Primary Antibody for 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 (show HSP90 Antibodies), stimulate APOBEC3 (show APOBEC3F Antibodies)-mediated DNA deamination activity toward hepatitis B viral DNA, suggesting a potential physiological role in mutagenesis/carcinogenesis and viral innate immunity; Hsp90 (show HSP90 Antibodies) stimulates deamination activity of APOBEC3G (show APOBEC3G Antibodies), APOBEC3B (show APOBEC3B Antibodies), 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 (show APOBEC3B Antibodies) and APOBEC3C involved in cancer mutagenesis is associated with estrogen receptor (show ESR1 Antibodies) status.
High APOBEC3C is associated with the pathogenesis of primary effusion lymphoma.
Expression of APOBEC3A (show APOBEC3A Antibodies) or 3C in 293FT cells reduced the infectivity of HPV16 pseudovirions. The reduced infectivity of virions assembled in the presence of APOBEC3A (show APOBEC3A Antibodies), but not 3C, was attributed to decreased copy number of the encapsidated reporter plasmid.
APOBEC3 (show APOBEC3F Antibodies) deaminases upregulated by IFN-beta (show IFNB1 Antibodies) 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 (show APOBEC3F Antibodies) 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 (show BTG1 Antibodies))-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