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anti-Human DFFB Antikörper:
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Human Monoclonal DFFB Primary Antibody für WB - ABIN266063
Yoshida, Urasaki, Waltham, Bergman, Pourquier, Rothwell, Inuzuka, Weinstein, Ueda, Appella, Hickson, Pommier: Human apurinic/apyrimidinic endonuclease (Ape1) and its N-terminal truncated form (AN34) are involved in DNA fragmentation during apoptosis. in The Journal of biological chemistry 2003
Show all 3 Pubmed References
Human Polyclonal DFFB Primary Antibody für WB - ABIN4892030
Yoon, Park, Han, Kang, Kim, Lee, Park, Shin, Kim, Yun, Chwae: Caspase-dependent cell death-associated release of nucleosome and damage-associated molecular patterns. in Cell death & disease 2014
we show that executioner caspase (zeige CASP3 Antikörper) activation of the apoptotic nuclease (zeige DCLRE1C Antikörper) CAD/DFF40 is essential for TRAIL-induced mutations in surviving cells. As exposure to chemotherapy drugs also activates apoptotic caspases and presumably CAD (zeige CAD Antikörper), we hypothesized that these pathways may also contribute to the mutagenesis induced by conventional chemotherapy drugs, perhaps augmenting the mutations that arise from direct DNA damage
Dff40 expression is upregulated in atherosclerotic plaque.
the low expression levels of DFF40/CAD and the absence of DNA laddering as common molecular traits in glioblastoma
Data suggest DFF40 expression in breast cancer cell line is involved in drug sensitivity/resistance to doxorubicin; apoptotic cell death due to doxorubicin (a topoisomerase II (zeige TOP2 Antikörper) inhibitor) is enhanced by DFF40 overexpression in breast cancer cell line.
Data show that the caspase-activated DNase (CAD) is activated when caspases cleave its endogenous inhibitor ICAD (zeige DFFA Antikörper), resulting in the characteristic DNA laddering of apoptosis.
Combinatorial use of some sulfonamides such as acetazolamide along with increased expression of DFF40 can potently kill tumor cells via apoptosis.
DFF40/CAD-independent mechanism driving conformational nuclear changes during caspase (zeige CASP3 Antikörper)-dependent cell death
the highest order of chromatin compaction observed in the later steps of caspase (zeige CASP3 Antikörper)-dependent apoptosis relies on DFF40/CAD-mediated DNA damage by generating 3'-OH ends in single-strand rather than double-strand DNA nicks/breaks
These results suggest a cooperative activity between CAD (zeige CAD Antikörper) and DNAS1L3 (zeige DNASE1L3 Antikörper) to accomplish internucleosomal DNA fragmentation .
Human papillomavirus type 16 E6 protein inhibits DNA fragmentation via interaction with DNA fragmentation factor (zeige DFFA Antikörper) 40
Dff40 expression is upregulated in atherosclerotic plaque. Dff40 deficiency inhibited high-fat diet-induced atherosclerosis, as evidenced by decreased atherosclerotic plaques, inhibited inflammatory response, and macrophage apoptosis, as well as enhanced stability of plaques.
results show that caspase 3 (zeige CASP3 Antikörper)/CAD (zeige CAD Antikörper) promotes cell differentiation by directly modifying the DNA/nuclear microenvironment, which enhances the expression of critical regulatory genes
Co-transfection of mouse DFF45 (zeige DFFA Antikörper)(-/-) fibroblasts with plasmids encoding human DFF40 and DFF45 (zeige DFFA Antikörper) reversed the apoptosis resistance normally observed in these cells
The thymus of DNase II(-/-)CAD (zeige CAD Antikörper)(-/-) embryos contained many foci carrying undigested DNA and the cellularity was severely reduced due to a block in T cell development.
Interactions identified here between mouse liver histone H1 (zeige H1F0 Antikörper) carboxyl-terminal domain and DFF40/CAD target and activate linker DNA cleavage during the terminal stages of apoptosis.
The results suggest that CAD protein (zeige CAD Antikörper) may be preferentially degraded by the ubiquitin-proteasome system in the absence of its inhibitor (ICAD (zeige DFFA Antikörper)) to maintain protein quality control.
A los of caspase-activated DNASE enhances tumorigenesis induced by a chemical carcinogen in a model of skin carcinogenesis in mice.
Apoptosis is a cell death process that removes toxic and/or useless cells during mammalian development. The apoptotic process is accompanied by shrinkage and fragmentation of the cells and nuclei and degradation of the chromosomal DNA into nucleosomal units. DNA fragmentation factor (DFF) is a heterodimeric protein of 40-kD (DFFB) and 45-kD (DFFA) subunits. DFFA is the substrate for caspase-3 and triggers DNA fragmentation during apoptosis. DFF becomes activated when DFFA is cleaved by caspase-3. The cleaved fragments of DFFA dissociate from DFFB, the active component of DFF. DFFB has been found to trigger both DNA fragmentation and chromatin condensation during apoptosis. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of these variants has not been determined.
DNA fragmentation factor subunit beta
, DNA fragmentation factor, 40 kD, beta polypeptide
, DNA fragmentation factor, 40kDa, beta polypeptide (caspase-activated DNase)
, DNA fragmentation factor 40 kDa subunit
, caspase-activated DNase
, caspase-activated deoxyribonuclease
, caspase-activated nuclease
, DNA fragmentation factor 40 kD beta polypeptide (caspase-activated DNase)
, DNA fragmentation factor, 40 kD, beta polypeptide (caspase-activated DNase)
, DNA fragmentation factor, beta polypeptide (caspase-activated DNase)
, DNA fragmentation factor, beta subunit
, DNA fragmentation factor, 40 kD, beta subunit
, DNase inhibited by DNA fragmentation factor