Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Wählen Sie die Spezies und Applikation aus
anti-Human BARD1 Antikörper:
anti-Mouse (Murine) BARD1 Antikörper:
anti-Rat (Rattus) BARD1 Antikörper:
Sie gelangen zu unserer vorgefilterten Suche.
Human Polyclonal BARD1 Primary Antibody für IP, PLA - ABIN151785
Hu, Ghosh, Amleh, Yue, Lu, Katz, Li: Modulation of aromatase expression by BRCA1: a possible link to tissue-specific tumor suppression. in Oncogene 2005
Show all 13 Pubmed References
Human Polyclonal BARD1 Primary Antibody für IHC, IHC (p) - ABIN4283035
Jerjees, Alabdullah, Green, Alshareeda, Macmillan, Ellis, Rakha: Prognostic and biological significance of proliferation and HER2 expression in the luminal class of breast cancer. in Breast cancer research and treatment 2014
Show all 2 Pubmed References
Human Polyclonal BARD1 Primary Antibody für IF (p), IHC (p) - ABIN706496
Liu, Ao, Jia, Bai, Xu, Hu, Jiang, Chen, Wu: FOXK2 transcription factor suppresses ER?-positive breast cancer cell growth through down-regulating the stability of ER? via mechanism involving BRCA1/BARD1. in Scientific reports 2015
variants in BARD1 were associated with moderate risks of breast cancer.
NPM1 (zeige NPM1 Antikörper) downregulation by P-STAT5 (zeige STAT5A Antikörper) is mediated by impairing the BRCA1-BARD1 ubiquitin ligase, which controls the stability of NPM1 (zeige NPM1 Antikörper). In turn, decreased NPM1 (zeige NPM1 Antikörper) levels led to suppression of p53 (zeige TP53 Antikörper) expression, resulting in enhanced cell survival.
In MCF-7 cells BARD1 variants do vary considerably their cellular distribution and in their ability to influence apoptotic response to cisplatin.
substitutions that create a structurally intact BRCA1/BARD1 heterodimer that is inactive in vitro with all E2 enzymes. Other substitutions in BRCA1 or BARD1 RING domains result in hyperactivity, revealing that both proteins have evolved attenuated activity. Loss of attenuation results in decreased product specificity, providing a rationale for why nature has tuned BRCA1 activity.
Findings suggest that the study of AtROW1 in plant may provide a model for elucidating the functional mechanism of BARD1 in mammals.
BRCA1-BARD1 ligase activity and subsequent SMARCAD1 (zeige SMARCAD1 Antikörper)-dependent chromatin remodeling are critical regulators of DNA repair in cancer cells.
Results suggest that BRCA1-associated RING domain protein 1 (BARD1) rs7585356 G>A polymorphism may be associated with nephroblastoma risk.
BARD1 rs6435862 T>G and rs3768716 A>G single nucleotide polymorphisms contribute to increased susceptibility to neuroblastoma (zeige ARHGEF16 Antikörper), especially for children at age >/=12 months in a Southern Chinese population.
BRCA pathway germline mutation (in BRCA1, BRCA2 (zeige BRCA2 Antikörper) or BARD1 genes) was present in 10 of the 42 investigated triple-negative breast cancer patients rendering them susceptible to homologous recombination deficiency.
Study presents four different pathogenic BARD1 variants identified in ovarian cancer patients. Three of them result in incorrect splicing of the corresponding exons, which may prompt expression of specific BARD1 isoforms and carcinogenesis.
Suggest BARD1 as a driver of proliferation and of pulmonary fibrosis pathogenesis.
identification of BARD1 as mediator between proapoptotic stress and p53 (zeige TP53 Antikörper)-dependent apoptosis
the developmental functions of Brca1 (zeige BRCA1 Antikörper) and Bard1 are mediated by the Brca1 (zeige BRCA1 Antikörper)/Bard1 heterodimer.
Data show that expression of truncated mouse or human BARD1 peptides capable of interacting with Brca1 results in a homologous-repair deficiency.
the ankyrin and BRCT motifs of BARD1 are each essential for both chromosome stability and homology-directed DNA repair.
The remarkable similarities between the mammary carcinomas of Bard1-, Brca1 (zeige BRCA1 Antikörper)-, and Bard1/Brca1 (zeige BRCA1 Antikörper)-mutant mice indicate that the tumor suppressor activities of both genes are mediated through the BRCA1 (zeige BRCA1 Antikörper)/BARD1 heterodimer.
This gene encodes a protein which interacts with the N-terminal region of BRCA1. In addition to its ability to bind BRCA1 in vivo and in vitro, it shares homology with the 2 most conserved regions of BRCA1: the N-terminal RING motif and the C-terminal BRCT domain. The RING motif is a cysteine-rich sequence found in a variety of proteins that regulate cell growth, including the products of tumor suppressor genes and dominant protooncogenes. This protein also contains 3 tandem ankyrin repeats. The BARD1/BRCA1 interaction is disrupted by tumorigenic amino acid substitutions in BRCA1, implying that the formation of a stable complex between these proteins may be an essential aspect of BRCA1 tumor suppression. This protein may be the target of oncogenic mutations in breast or ovarian cancer.
BRCA1 associated RING domain 1
, BRCA1-associated RING domain protein 1-like
, BRCA1 associated RING domain 1 isoform alfa
, BRCA1 associated RING domain 1 isoform beta
, BRCA1 associated RING domain 1 isoform delta
, BRCA1 associated RING domain 1 isoform epsilon
, BRCA1 associated RING domain 1 isoform eta
, BRCA1 associated RING domain 1 isoform gamma
, BRCA1 associated RING domain 1 isoform phi
, BRCA1-associated RING domain gene 1
, BRCA1-associated RING domain protein 1