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抗Mouse (Murine) BIK 抗体:
抗Human BIK 抗体:
抗Rat (Rattus) BIK 抗体:
Human Monoclonal BIK Primary Antibody for IP, WB - ABIN967566
Boyd, Gallo, Elangovan, Houghton, Malstrom, Avery, Ebb, Subramanian, Chittenden, Lutz: Bik, a novel death-inducing protein shares a distinct sequence motif with Bcl-2 family proteins and interacts with viral and cellular survival-promoting proteins. in Oncogene 1995
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Human Polyclonal BIK Primary Antibody for ICC, ELISA - ABIN1001872
Lockshin, Osborne, Zakeri: Cell death in the third millennium. in Cell death and differentiation 2000
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Human Polyclonal BIK Primary Antibody for IHC (fro), WB - ABIN2477650
Unsicker, Stögbauer: Screening of adrenal medullary neuropeptides for putative neurotrophic effects. in International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 1992
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Human Polyclonal BIK Primary Antibody for ICC, ELISA - ABIN1031274
Chen, Zhou, Zhang, Leng, Pei, Lin, Jones, Orlowski, Dai, Grant: Targeting SQSTM1/p62 induces cargo loading failure and converts autophagy to apoptosis via NBK/Bik. in Molecular and cellular biology 2014
Human Polyclonal BIK Primary Antibody for WB - ABIN223382
Chen, Huang, Wang: Deficiency of Bim in dendritic cells contributes to overactivation of lymphocytes and autoimmunity. in Blood 2007
Human Polyclonal BIK Primary Antibody for IHC (p), WB - ABIN388114
Gillissen, Essmann, Graupner, Stärck, Radetzki, Dörken, Schulze-Osthoff, Daniel: Induction of cell death by the BH3-only Bcl-2 homolog Nbk/Bik is mediated by an entirely Bax-dependent mitochondrial pathway. in The EMBO journal 2003
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These studies suggest a link between Bik-mediated caspase (显示 CASP3 抗体) activation and cleavage of viral proteins.
OPN (显示 SPP1 抗体) induces oxidative stress via the involvement of mitochondria and NOX-4 (显示 NOX4 抗体). It may affect mitochondrial morphology and integrity, at least in part, via the involvement of BIK.
Findings identify novel cross talk between autophagy and apoptosis, wherein targeting SQSTM1/p62 (显示 SQSTM1 抗体) converts cytoprotective autophagy to an inefficient form due to cargo loading failure, leading to NBK/Bik accumulation, which triggers apoptosis.
Src (显示 SRC 抗体) tyrosine kinase (显示 TYRO3 抗体) inhibits apoptosis through the Erk1/2 (显示 MAPK1/3 抗体)- dependent degradation of the death accelerator Bik.
The Bik protein, even in combination with Noxa (显示 PMAIP1 抗体), is not a potent suppressor of c-Myc (显示 MYC 抗体)-driven tumourigenesis or critical for chemotherapeutic drug-induced killing of Myc (显示 MYC 抗体)-driven tumours.
BIKDD, a constitutively active mutant form of proapoptotic gene, BIK, effectively induces apoptosis of breast cancer cells and synergizes with lapatinib.
Blk has been mapped to chromosome 15 and overexpressed in transitional B cells of A/WySnJ mice, which demonstrate a cell-autonomous defect leading to excessive apoptosis.
any function of Bik in programmed cell death and stress-induced apoptosis must overlap that of other BH3-only (显示 BBC3 抗体) proteins
Data show that Bik and Bim (显示 BCL2L11 抗体) share the role of eliminating supernumerary germ cells during the first wave of spermatogenesis, a process vital for normal testicular development.
Targeted expression of BikDD, a potent proapoptotic gene driven by CCKAR (显示 CCKAR 抗体)-VISA (显示 MAVS 抗体), exhibited antitumor effects on pancreatic cancer and prolonged survival in multiple xenograft and syngeneic mouse models of pancreatic tumors with virtually no toxicity
BIK significantly contributes to DNA damage-induced mitochondrial apoptosis in HCT-116 wt cells upstream of the second peak of ROS (显示 ROS1 抗体) production, BAX (显示 BAX 抗体) and BAK (显示 BAK1 抗体) activation, cytochrome c (显示 CYCS 抗体) release and caspase (显示 CASP3 抗体) activation.
our data demonstrated that suppression of BIK in ER-positive MCF-7 cells prevents the cytotoxic effect of TAM (显示 CCNA1 抗体) and favors a more aggressive phenotype, due to the molecular change of different pathways
HCV RNA replication and release were significantly suppressed in BIK-depleted cells and over-expression of the RNA-dependent RNA polymerase, NS5B, was able to induce BIK expression
BikDDA, a novel mutant of Bik, showed a prolonged half-life and enhanced pro-apoptotic ability in triple-negative breast cancer cells compared with BikDD.
Authors show that human herpesvirus 4 EBNA2 represses BIK in B-cell lymphoma-derived cell lines and that this host-virus interaction can inhibit the proapoptotic effect of transforming growth factor beta1.
Data suggest BIK expression in tumor cells is not subject to direct regulation by MAP kinase (显示 MAPK1 抗体) signaling; BIK expression appears to be cell-cycle-dependent and increases in G1 cell-cycle arrest which results from inhibition of MAP kinase (显示 MAPK1 抗体) signaling.
BIK/NBK gene expression may have important clinical implications and provide predictive, prognostic or therapeutic marker in breast cancer patients
Src (显示 SRC 抗体) tyrosine kinase (显示 TXK 抗体) inhibits apoptosis through the Erk1/2 (显示 MAPK1/3 抗体)- dependent degradation of the death accelerator Bik.
The protein encoded by this gene shares a critical BH3 domain with other death-promoting proteins, such as BID, BAK, BAD and BAX, that is required for its pro-apoptotic activity, and for interaction with anti-apoptotic members of the BCL2 family, and viral survival-promoting proteins. Since the activity of this protein is suppressed in the presence of survival-promoting proteins, it is suggested as a likely target for anti-apoptotic proteins.
BCL2-interacting killer (apoptosis-inducing)
, BCL2-interacting killer
, apoptosis inducer NBK
, bcl-2-interacting killer
, bik-like killer protein
, apoptosis-inducing NBK