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APOBEC3C is a member of the cytidine deaminase gene family. Additionally we are shipping APOBEC3C Antibodies (76) and many more products for this protein.
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Data suggest that heat shock proteins, in particular Hsp90 (show HSP90 Proteins), stimulate APOBEC3 (show APOBEC3F Proteins)-mediated DNA deamination activity toward hepatitis B viral DNA, suggesting a potential physiological role in mutagenesis/carcinogenesis and viral innate immunity; Hsp90 (show HSP90 Proteins) stimulates deamination activity of APOBEC3G (show APOBEC3G Proteins), APOBEC3B (show APOBEC3B Proteins), 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 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 or 3C in 293FT cells reduced the infectivity of HPV16 pseudovirions. The reduced infectivity of virions assembled in the presence of APOBEC3A, 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.
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