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The protein encoded by FAIM protects against death receptor-triggered apoptosis and regulates B-cell signaling and differentiation. Zusätzlich bieten wir Ihnen FAIM Proteine (8) und FAIM Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal FAIM Primary Antibody für ELISA, WB - ABIN1002284
Rothstein: Inducible resistance to Fas-mediated apoptosis in B cells. in Cell research 2001
Show all 2 Pubmed References
Human Polyclonal FAIM Primary Antibody für IHC (p), IHC - ABIN262283
Schneider, Fischer, Donohoe, Colarusso, Rothstein: A novel gene coding for a Fas apoptosis inhibitory molecule (FAIM) isolated from inducibly Fas-resistant B lymphocytes. in The Journal of experimental medicine 1999
the anti-apoptotic effect of SRT1720 was mitigated by FAIM knockdown with a small interfering RNA-targeted FAIM. These results indicated that pretreatment with SRT1720 improves survival of aged hMSCs, and enhances their therapeutic efficacy for rat myocardial infarction (MI).
subcellular fractionation experiments revealed that, in contrast to FAIM-S and FAIM-L, FAIM-S_2a and FAIM-L_2a are able to localize to the nucleus, where they may have additional functions. In summary, here we report on two novel FAIM isoforms that may have relevant roles in the physiology and pathology of the nervous system
Data indicate that FAIM is a novel regulator of insulin (zeige INS Antikörper) signalling and plays an essential role in energy homoeostasis.
FAIM modulates IGF-1 (zeige IGF1 Antikörper)-induced Akt (zeige AKT1 Antikörper) activation and IRF4 (zeige IRF4 Antikörper) expression and has a role in multiple myeloma cell survival
FAIM (1-90) was crystallized and diffracted to a resolution of 2.5 A; the crystal belonged to space group P3(1), with unit-cell parameters a=b=58.02, c=71.11 A, alpha=beta=90, gamma=120 degrees.
Human keratinocytes were transfected with either Flip, Faim, or Lifeguard (LFG (zeige FAIM2 Antikörper)). Our results suggest that heterotopic expression of antiapoptotic proteins can induce the resistance of keratinocytes to a major mechanism of rejection.
Expression of the long form of Fas apoptotic inhibitory molecule (FAIML) results in the protection of neurons from the cytotoxic actions of death ligands.
FAIM acts to specifically enhance CD40 (zeige CD40 Antikörper) signaling for NF-kappaB (zeige NFKB1 Antikörper) activation, IRF-4 (zeige IRF4 Antikörper) expression, and BCL-6 (zeige BCL6 Antikörper) down-regulation in vitro, but has no effect on its own
defined a TCR-induced FAIM/Akt (zeige AKT1 Antikörper)/Nur77 (zeige NR4A1 Antikörper) signaling axis that is critical for modulating the apoptosis of developing thymocytes
The NMR solution structure of the C-terminal domain of murine FAIM is solved in isolation and revealed to be a novel protein fold, a noninterleaved seven-stranded beta-sandwich.
FAIM plays a novel role in modulating Fas (zeige FAS Antikörper)-mediated apoptosis and acts through influencing the expression of c-FLIP (zeige CFLAR Antikörper) and regulating the physical binding of caspase-8 (zeige CASP8 Antikörper) to Fas (zeige FAS Antikörper).
FAIM is expressed in germinal center B cells, enhances interferon (zeige IFNA Antikörper) regulatory factor (IRF)4 (zeige IRF4 Antikörper) expression, and is in turn positively regulated through IRF4 (zeige IRF4 Antikörper) in a positive reinforcing (i.e., feed-forward) system.
The protein encoded by this gene protects against death receptor-triggered apoptosis and regulates B-cell signaling and differentiation. Several transcript variants encoding different isoforms have been found for this gene.
fas apoptotic inhibitory molecule 1
, Fas apoptotic inhibitory molecule
, Fas apoptosis inhibitory molecule 1