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GFAP encodes one of the major intermediate filament proteins of mature astrocytes. Zusätzlich bieten wir Ihnen GFAP Kits (68) und GFAP Proteine (39) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal GFAP Primary Antibody für IHC (p), WB - ABIN3044350
Zhou, Wang, Li, Wang, Wu, Zhang: Paeoniflorin attenuates the neuroinflammatory response in a rat model of chronic constriction injury. in Molecular medicine reports 2017
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Cat (Feline) Polyclonal GFAP Primary Antibody für IEM, ICC - ABIN789007
Segal, Takahashi, McKay: Changes in neurotrophin responsiveness during the development of cerebellar granule neurons. in Neuron 1993
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Human Polyclonal GFAP Primary Antibody für IHC (p), WB - ABIN3043832
Lu, Yuan, Ou, Cai, Wang, Sun, Zhang: Autophagy and apoptosis during adult adipose-derived stromal cells differentiation into neuron-like cells in vitro. in Neural regeneration research 2015
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Human Monoclonal GFAP Primary Antibody für IHC (fro), IHC (p) - ABIN3043647
Zhao, Guo, Li, Zang, Qu, Zhou, Li, Sun: Amelioration of dementia induced by A? 22-35 through rectal delivery of undecapeptide-hEGF to mouse brain. in International journal of pharmaceutics 2011
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Cat (Feline) Polyclonal GFAP Primary Antibody für ICC, IF - ABIN152487
Henion, Qu, Smith: Expression of dystroglycan, fukutin and POMGnT1 during mouse cerebellar development. in Brain research. Molecular brain research 2003
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Mammalian Monoclonal GFAP Primary Antibody für ISt, IHC - ABIN1304664
Savic, Stojiljkovic, Lavrnja, Parabucki, Bjelobaba, Nedeljkovic, Herdegen, Pekovic: Ribavirin shows immunomodulatory effects on activated microglia. in Immunopharmacology and immunotoxicology 2014
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Human Polyclonal GFAP Primary Antibody für FACS, IF (cc) - ABIN726200
Zhao, Zhao, Wang, Xu, Miao, Feng, Chen, Kovács, Fan, Zhang: Mice deficient in Epg5 exhibit selective neuronal vulnerability to degeneration. in The Journal of cell biology 2013
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Chicken Polyclonal GFAP Primary Antibody für ICC, IP - ABIN1742363
Christensen, Schneider-Axmann, Lucassen, Bayer, Wirths: Accumulation of intraneuronal Abeta correlates with ApoE4 genotype. in Acta neuropathologica 2010
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Bird (Avian) Monoclonal GFAP Primary Antibody für ICC, IF - ABIN446355
Brai, Marathe, Zentilin, Giacca, Nimpf, Kretz, Scotti, Alberi: Notch1 activity in the olfactory bulb is odour-dependent and contributes to olfactory behaviour. in The European journal of neuroscience 2014
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Human Monoclonal GFAP Primary Antibody für ICC, IHC (p) - ABIN457420
Bignami, Eng, Dahl, Uyeda: Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence. in Brain research 1972
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There was significantly more GFAP immunoreactivity in the prefrontal cortex and hippocampus of aged animals compared to adult or middle-aged animals.
These results indicate that autoantibodies against GFAP could serve as a predictive marker for the development of overt autoimmune diabetes.
Higher median plasma GFAP values were documented in intracerebral hemorrhage compared with acute ischemic stroke, stroke mimics, and controls.
GFAP is specifically expressed in the auricular chondrocytes, and assumes a pivotal role in resistance against mechanical stress.
Bevacizumab treatment was also associated with structural protein abnormalities, with decreased GFAP and vimentin (zeige VIM Antikörper) content and upregulated GFAP and vimentin (zeige VIM Antikörper) mRNA expression.
Tat (zeige TAT Antikörper) expression or GFAP expression led to formation of GFAP aggregates and induction of unfolded protein response (UPR) and endoplasmic reticulum (ER) stress in astrocytes.
This study demonstrated that GFAP exhibited distinct temporal profiles over the course of 7 days in patient with traumatic brain injury.
e data indicates that serum GFAP levels may be associated with severity of autism spectrum disorders among Chinese children.
High GFAP expression is associated with retinoblastoma.
Overall, glial fibrillary acidic protein reflected no evidence for significant peripartum brain injury in neonates with congenital heart defects, but there was a trend for elevation by postnatal day 4 in neonates with left heart obstruction.
serum levels of GFAP were significantly lower in autism spectrum disorders than controls
Isolation of an evolutionary conserved novel GFAP isoform, GFAPkappa, produced by alternative splicing and polyadenylation of the 3'-region of the human GFAP pre-mRNA is described.
compared open-skull and thinned-skull imaging methods for two-photon laser microscopy of live astrocytes in neocortex of GFAP-GFP transgenic mice
work reveals that an Alexander disease-causing mutation alters GFAP turnover kinetics in vivo and provides an essential foundation for future studies aimed at preventing or reducing the accumulation of GFAP.
Study provides evidence that transcription of one of the astrocyte-specific genes, Gfap, is cooperatively regulated by co-expressed genes and their regulatory factors.
This study demonstrated the GFAP-ApoE4 mice exhibited motor impairments when compared to GFAP-ApoE3 and wild-type mice.
PINK1 (zeige PINK1 Antikörper) deficiency causes defects in GFAP-positive astrogliogenesis during brain development.
Gnasxl (zeige GNAS Antikörper) deficiency does not directly affect glial development in the hypothalamus, since it is expressed in neurons, and Gfap-positive astrocytes and tanycytes appear normal during early postnatal stages.
Induction of glial cytokine expression was sequential, aligned with active sickness behavior, and preceded increased Iba-1 (zeige AIF1 Antikörper) or GFAP immunoreactivity after lipopolysaccharide challenge
The distribution of GFAP immunoreactivity implies that enteric glia are widespread in the fish gastrointestinal tract.
Generation of transgenic zebrafish that express green fluorescent protein (GFP) in glial cells driven by the zebrafish glial fibrillary acidic protein (GFAP) regulatory elements.
Cells expressing the two reporters display radial glial morphology, colocalize with the NSC marker Sox2 (zeige SOX2 Antikörper), undergo proliferation, and are capable of self-renewal within the matrix of distinct thickness in the telencephalon.
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
glial fibrillary acidic protein
, glial fibrillary acidic protein alpha
, intermediate filament
, intermediate filament protein
, zrf-1 antigen