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APOBEC3C is a member of the cytidine deaminase gene family. Additionally we are shipping APOBEC3C Antibodies (57) and many more products for this protein.
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These results suggest that functional potential of APOBEC3B (show APOBEC3B Proteins) and APOBEC3C involved in cancer mutagenesis is associated with estrogen receptor (show ESR1 Proteins) status.
High APOBEC3C is associated with the pathogenesis of primary effusion lymphoma.
Expression of APOBEC3A (show APOBEC3A Proteins) or 3C in 293FT cells reduced the infectivity of HPV16 pseudovirions. The reduced infectivity of virions assembled in the presence of APOBEC3A (show APOBEC3A Proteins), but not 3C, was attributed to decreased copy number of the encapsidated reporter plasmid.
APOBEC3 (show APOBEC3F Proteins) deaminases upregulated by IFN-beta (show IFNB1 Proteins) 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 Proteins) 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 Proteins))-interaction interface.
Findings suggest that APOBEC3 (show APOBEC3F Proteins)-mediated editing of HIV-1 could be modulated by host and virus genetic characteristics in the context of pediatric infection.
The result suggest that Core-A3C may be a candidate as a novel antiviral agent against human HBV infection.
Somatic hypermutation of human mitochondrial and nuclear DNA by APOBEC3 (show APOBEC3F Proteins) cytidine deaminases, a pathway for DNA catabolism.
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