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APOBEC1 encodes a member of the cytidine deaminase enzyme family. Additionally we are shipping APOBEC1 Proteins (7) and many more products for this protein.
Showing 10 out of 57 products:
Human Polyclonal APOBEC1 Primary Antibody for EIA, IHC (p) - ABIN356861
Blanc, Kennedy, Davidson: A novel nuclear localization signal in the auxiliary domain of apobec-1 complementation factor regulates nucleocytoplasmic import and shuttling. in The Journal of biological chemistry 2003
Show all 5 references for ABIN356861
Human Polyclonal APOBEC1 Primary Antibody for WB - ABIN2778780
Schafmayer, Völzke, Buch, Egberts, Spille, von Eberstein, Franke, Seeger, Hinz, Elsharawy, Rosskopf, Brosch, Krawczak, Foelsch, Schafmayer, Lammert, Schreiber, Faendrich, Hampe, Tepel: Investigation of the Lith6 candidate genes APOBEC1 and PPARG in human gallstone disease. in Liver international : official journal of the International Association for the Study of the Liver 2007
Human Polyclonal APOBEC1 Primary Antibody for WB - ABIN375056
Lau, Chan: Involvement of a chaperone regulator, Bcl2-associated athanogene-4, in apolipoprotein B mRNA editing. in The Journal of biological chemistry 2003
Apobec-1-dependent C-to-U RNA editing exerts broad functional effects in a tissue-specific manner.
RBM47 and APOBEC1 constitute the basic machinery for C to U RNA editing.
In contrast to in vitro results, APOBEC1 neither inhibited nor significantly drove the molecular evolution of Friend retrovirus in wild type or APOBEC1 knockout mice.
Individual genetic variability at the Apobec1 locus results in differential rates of C-to-U(T) editing in murine macrophages; with mouse strains expressing mostly a truncated alternative transcript isoform of Apobec1 exhibiting lower rates of editing.
The transgenic rescue of intestinal apobec-1 expression restores C-to-U RNA editing of apoB (show APOB Antibodies) mRNA in vivo, including the canonical site at position 6666 and also at approximately 20 other newly identified downstream sites present in WT mice.
Results suggest that apo (show C9orf3 Antibodies) B mRNA editing protein (Apobec1 cytidine deaminase (show CDA Antibodies)) plays a central role in controlling testicular germ cell tumors susceptibility in both a conventional and a transgenerational manner.
The transcriptomics approach to RNA editing presented in this study dramatically expands the list of APOBEC1 mRNA editing targets and reveals a novel cellular mechanism for the modification of transcript 3' UTRs.
LDL receptor (show LDLR Antibodies) and the apolipoprotein B (show APOB Antibodies) mRNA editing enzyme Apobec1 are regulated via calcium signaling in mechanistic response to genetic, mechanical, and environmental insults that trigger an imbalance of intracellular calcium homeostasis
studies establish the existence of preferential degradation of intestinal apolipoprotein B-100 (show APOB Antibodies) and subtle defects in triglyceride secretion in apolipoprotein B editing complex 1-/- mice
apobec-1 complementation factor (show A1CF Antibodies) has a role in regulating nucleocytoplasmic import and shuttling
AICDA (show AICDA Antibodies)/APOBEC family of cytidine deaminases is significant in innate immunity, as it restricts numerous viruses, including HBV, through hypermutationdependent and independent mechanisms. (Review)
Results show that expression of APOBEC1 induces a mutator phenotype in 2 different cellular models.
hnRNPQ6 is required for APOBEC1-enhanced IL8 (show IL8 Antibodies) production.
Studies indicate the APOBEC family consists of 11 members: APOBEC-1 (Apo1), APOBEC-2 (Apo2), activation induced cytidine deaminase (AID), APOBEC- 3A, -3B, -3C, -3DE, -3F, -3H (Apo3A-H) and APOBEC- 4 (Apo4).
The hypermutation activity of APOBEC-1 was decreased to background levels by a single point APOBEC-1 mutation of P29F or E181Q, while 50% of wild-type control editing at the normal site was retained.
The data presented in this report suggested that similar regulatory mechanisms controlling the functional interaction of APOBEC-1 with ACF (show A1CF Antibodies) might be operational during enterocyte differentiation.
Identified two novel variants, rs1349411 (APOBEC1) and rs1424032, for serum apoB (show APOB Antibodies) levels in Mexicans.
C-->U editing of neurofibromatosis 1 (show NF1 Antibodies) mRNA occurs in tumors that express both the type II transcript and apobec-1, the catalytic subunit of the apolipoprotein B (show APOB Antibodies) mRNA-editing enzyme
expression of two proteins essential for apolipoprotein B (show APOB Antibodies) mRNA editing from a single gene through alternative splicing
A moderate reduction of the APOBEC1 dependent editing induces a lean phenotype at least in the rabbit species.
This gene encodes a member of the cytidine deaminase enzyme family. The encoded protein forms a multiple-protein editing holoenzyme with APOBEC1 complementation factor (ACF) and APOBEC1 stimulating protein (ASP). This holoenzyme is involved in the editing of C-to-U nucleotide bases in apolipoprotein B and neurofibromatosis-1 mRNAs.
apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1
, C->U-editing enzyme APOBEC-1
, apolipoprotein B mRNA editing enzyme complex 1
, apolipoprotein B mRNA-editing enzyme 1
, APOBEC1 complementation factor
, apobec-1 complementation factor
, APOBEC1-stimulating protein
, apobec-1 complementation factor-like
, APOBEC1 complementation factor-like
, apolipoprotein B editing complex 1
, apolipoprotein B mRNA editing enzyme complex-1
, apolipoprotein B mRNA editing protein
, Apolipoprotein B editing protein
, Apolipoprotein B mRNA-editing enzyme 1
, apolipoprotein B mRNA editing catalytic subunit-1