Use your antibodies-online credentials, if available.
Il n’y a pas de produits dans votre liste de comparaison.
Votre panier est vide.
GFAP encodes one of the major intermediate filament proteins of mature astrocytes. De plus, nous expédions GFAP Kits (65) et GFAP Protéines (38) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 805 products:
Human Monoclonal GFAP Primary Antibody pour IF, WB - ABIN1449159
Macaulay, Forbes: Assembly of the nuclear pore: biochemically distinct steps revealed with NEM, GTP gamma S, and BAPTA. dans The Journal of cell biology 1996
Show all 11 references for 1449159
Human Monoclonal GFAP Primary Antibody pour IF, WB - ABIN1449150
Kawajiri, Yasui, Goto, Tatsuka, Takahashi, Nagata, Inagaki: Functional significance of the specific sites phosphorylated in desmin at cleavage furrow: Aurora-B may phosphorylate and regulate type III intermediate filaments during cytokinesis coordinatedly with Rho-kinase. dans Molecular biology of the cell 2003
Show all 6 references for 1449150
Cow (Bovine) Monoclonal GFAP Primary Antibody pour IHC (fro), IF - ABIN111187
Akat, Mennel, Kremer, Gassler, Bleck, Kartenbeck: Molecular characterization of desmosomes in meningiomas and arachnoidal tissue. dans Acta neuropathologica 2003
Show all 6 references for 111187
Human Polyclonal GFAP Primary Antibody pour EIA - ABIN358488
Quintanar, Franco, Salinas: Detection of glial fibrillary acidic protein and neurofilaments in the cerebrospinal fluid of patients with neurocysticercosis. dans Parasitology research 2003
Show all 5 references for 358488
Human Monoclonal GFAP Primary Antibody pour IHC (fro), IHC (p) - ABIN1107345
Rodriguez, Gauthier, Bertini, Bugiani, Brenner, Nguyen, Goizet, Gelot, Surtees, Pedespan, Hernandorena, Troncoso, Uziel, Messing, Ponsot, Pham-Dinh, Dautigny, Boespflug-Tanguy: Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation. dans American journal of human genetics 2001
Show all 2 references for 1107345
Cat (Feline) Monoclonal GFAP Primary Antibody pour IHC (fro), IHC (p) - ABIN111957
Li, Chou, Luk, Wang, Xie, McDougall, Huang: Design of intracavitary microwave applicators for the treatment of uterine cervix carcinoma. dans International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group 1991
Human Monoclonal GFAP Primary Antibody pour IHC (fro), IHC (p) - ABIN114688
Van Muijen, Ruiter, Warnaar: Coexpression of intermediate filament polypeptides in human fetal and adult tissues. dans Laboratory investigation; a journal of technical methods and pathology 1987
Human Monoclonal GFAP Primary Antibody pour IHC (p) - ABIN1689203
Stoletov, Strnadel, Zardouzian, Momiyama, Park, Kelber, Pizzo, Hoffman, VandenBerg, Klemke: Role of connexins in metastatic breast cancer and melanoma brain colonization. dans Journal of cell science 2013
Human Monoclonal GFAP Primary Antibody pour IHC (fro), IF - ABIN238409
Porchet, Probst, Bouras, Dráberová, Dráber, Riederer: Analysis of glial acidic fibrillary protein in the human entorhinal cortex during aging and in Alzheimer's disease. dans Proteomics 2003
Human Polyclonal GFAP Primary Antibody pour IHC, ELISA - ABIN185730
Korolainen, Auriola, Nyman, Alafuzoff, Pirttilä: Proteomic analysis of glial fibrillary acidic protein in Alzheimer's disease and aging brain. dans Neurobiology of disease 2005
There was significantly more GFAP immunoreactivity in the prefrontal cortex and hippocampus of aged animals compared to adult or middle-aged animals.
Bevacizumab treatment was also associated with structural protein abnormalities, with decreased GFAP and vimentin (Montrer VIM Anticorps) content and upregulated GFAP and vimentin (Montrer VIM Anticorps) mRNA expression.
Tat (Montrer TAT Anticorps) 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
We found downregulation of GFAP mRNA and protein in the mediodorsal thalamus and caudate nucleus of depressed suicides compared with controls, whereas GFAP expression in other brain regions was similar between groups. Furthermore, a regional comparison including all samples revealed that GFAP expression in both subcortical regions was, on average, between 11- and 15-fold greater than in cerebellum and neocortex.
GFAP is upregulated following an insult or injury to the brain, additionally making it an indicator of CNS pathology.
This study demonistrated that the density of GFAP-immunoreactive astrocytes is decreased in left hippocampi in major depressive disorder
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 (Montrer PINK1 Anticorps) deficiency causes defects in GFAP-positive astrogliogenesis during brain development.
Gnasxl (Montrer GNAS Anticorps) 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 (Montrer AIF1 Anticorps) or GFAP immunoreactivity after lipopolysaccharide challenge
Study provides a mechanistic link between the GFAP mutations/overexpression and the symptoms in those affected with Type II Alexander disease
Study described GFAP-expressing non-myelinating Schwann cells in the lung, validated a transgenic mouse line that drives expression of cre under a GFAP promoter
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 (Montrer SOX2 Anticorps), 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