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        Rabbit Anti-GFAP antibody (bs-0199R)
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        说明书: 50ul  100ul  200ul
        50ul/980.00元
        100ul/1680.00元
        200ul/2480.00元
        大包装/询价

        产品编号 bs-0199R
        英文名称 GFAP
        中文名称 胶质纤维酸性蛋白抗体
        别    名 Astrocyte; FLJ45472; GFAP; Glial Fibrillary Acidic Protein; Intermediate filament protein; GFAP_HUMAN.  
        Specific References  (29)     |     bs-0199R has been referenced in 29 publications.
        [IF=2.766] Xiang Y et al. Inhibition of sPLA. sub. 2-IIA Prevents LPS-Induced Neuroinflammation by Suppressing ERK1/2-cPLA. sub. 2 [alpha] Pathway in Mice Cerebral Cortex.PLoS One. 2013 Oct 9;8(10):e77909.   Other ;  
        [IF=2.234] Lu et al. Autophagy activator promotes neuronal differentiation of adult adipose-derived stromal cells. (2013) Neural.Regen.Res. 8:882-9  ICC ;  Human.  
        [IF=1.77] Liang et al. Scorpion ethanol extract and valproic acid effects on hippocampal glial fibrillary acidic protein expression in a rat model of chronic-kindling epilepsy induced by lithium chloride-pilocarpine. (2012) Neural.Regen.Re. 7:426-33  IHC ;  rat.  
        [IF=3.974] Esaki,et al.ASC amino acid transporter 2, defined by enzyme-mediated activation of radical sources, enhances malignancy of GD2-positive small-cell lung cancer.(2018) Cancer Science. 109:141-153.  IF(ICC) ;  Human.  
        [IF=3.562] Zhang,et al.Interferon-γ Promotes Neuronal Repair by Transplanted Neural Stem Cells in Ischemic Rats.(2018) Stem Cells and Development. 27:355-366.  IF(ICC) ;  Rat.  
        [IF=2.81] Farah et al. Tau accumulations in the brains of woodpeckers. (2018) PLoS.One. 13:e0191526  IHC-P ;  Woodpecker.  
        [IF=2.341] Zhong,et al.Protective effect of adenovirus-mediated erythropoietin expression on the spiral ganglion neurons in the rat inner ear.(2018) International Journal of Molecular Medicine. 41:2669-2677.  IHC-P + IF(IHC-P) ;  Rat.  
        [IF=1.97] Liao et al. The effect of celastrol on learning and memory in diabetic rats after sevoflurane inhalation. (2018) Arch.Med.Sci. 14:370-380  IHC ;  Rat.  
        [IF=1.812] Liao, Wei-Tao, et al. "The effect of celastrol on learning and memory in diabetic rats after sevoflurane inhalation." (2016).  IHC-P ;  Rat.  
        [IF=3.44] Zhang X et al.Neuroprotective effects of matrix metalloproteinases in cerebral ischemic rats by promoting activation and migration of astrocytes and microglia.(2018) Brain Res Bull. Nov 13.  WB ;  Rat.  
        [IF=2.064] Yao Q et al.Lycium Barbarum Polysaccharides Improve Retinopathy in Diabetic Sprague-Dawley Rats.(2018)Evid Based Complement Alternat Med.Nov 15;2018:7943212.   WB ;  Rat.  
        [IF=2.159] Iwasa T et al. IL-10 and CXCL2 in trigeminal ganglia in neuropathic pain.Neurosci Lett.?2019 Jun 11;703:132-138.?  IHC-P ;  Rat.  
        [IF=4.65] Zhao, Yan G., et al. "The p53-induced gene Ei24 is an essential component of the basal autophagy pathway." Journal of Biological Chemistry 287.50 (2012): 42053-42063.  Mouse.  
        [IF=10.82] Zhao, Hongyu, et al. "Mice deficient in Epg5 exhibit selective neuronal vulnerability to degeneration." The Journal of Cell Biology (2013).  IHC-P ;  Mouse.  
        [IF=2.93] Liu, Yang, et al. "A Simple Method for Isolating and Culturing the Rat Brain Microvascular Endothelial Cells." Microvascular Research (2013).  Rat.  
        [IF=2.89] Xiang, Yanxiao, et al. "Anti-inflammatory Effect of Acetylpuerarin on Eicosanoid Signaling Pathway in Primary Rat Astrocytes."Journal of Molecular Neuroscience(2013): 1-9  Mouse.  
        [IF=3.73] Xiang, Yanxiao, et al. "Anti-inflammatory Effect of Acetylpuerarin on Eicosanoid Signaling Pathway in Primary Rat Astrocytes."Journal of Molecular Neuroscience(2013): 1-9  IF(ICC) ;  Rat.  
        [IF=1.29] Fan, Lixing, et al. "Directed differentiation of aged human bone marrow multipotent stem cells effectively generates dopamine neurons."?In Vitro Cellular & Developmental Biology-Animal?(2013): 1-9.  Human.  
        [IF=2.65] Zuo, Daiying, et al. "Existence of glia mitigated ketamine-induced neurotoxicity in neuron-glia mixed cultures of neonatal rat cortex and the glia-mediated protective effect of 2-PMPA." Neurotoxicology (2014).  Rat.  
        [IF=10.53] Ma, Benyu, et al. "Dapper1 promotes autophagy by enhancing the Beclin1-Vps34-Atg14L complex formation." Cell Research (2014).  IHC-F ;  Mouse.  
        [IF=5.29] Du, Wenzhong, et al. "Targeting the SMO oncogene by miR-326 inhibits glioma biological behaviors and stemness." Neuro-Oncology (2014): nou217.  IHC-F ;  Human.  
        [IF=7.58] Shan, Chun-Lei, et al. "High Efficiency Intracellular Transport of Cationic Peptide Stearate for Gene Delivery in Tumor Cells and Multipotent Stem Cells." Journal of Biomedical Nanotechnology 10.11 (2014): 3231-3243.  other ;  
        [IF=11.42] Zhao, Yan G., et al. "The autophagy gene Wdr45/Wipi4 regulates learning and memory function and axonal homeostasis." Autophagy (2015).  IHC-P ;  Mouse.  
        [IF=2.86] Mori, Miki, et al. "Stromal Cell-Derived Factor-1α Plays a Crucial Role Based on Neuroprotective Role in Neonatal Brain Injury in Rats." International Journal of Molecular Sciences 16.8 (2015): 18018-18032.  IHC-F ;  Rat.  
        [IF=2.47] Yan, Yu-hui, et al. "Osthole Protects Bone Marrow-Derived Neural Stem Cells from Oxidative Damage through PI3K/Akt-1 Pathway." Neurochemical Research (2016): 1-8.  other ;  Mouse.  
        [IF=2.86] Hu. et al. Levo-Corydalmine Alleviates Neuropathic Cancer Pain Induced by Tumor Compression via the CCL2/CCR2 Pathway  IF(IHC-P) ;  Mouse.  
        [IF=3.811] Sun Z et al. Glioblastoma Stem Cell-Derived Exosomes Enhance Stemness and Tumorigenicity of Glioma Cells by Transferring Notch1 Protein. Cell Mol Neurobiol. 2019 Dec 18.   WB ;  Human&Mouse.  
        [IF=.181] H Mu et al. HCMV-encoded IE2 induces anxiety-depression and cognitive impairment in UL122 genetically-modified mice. Int J Clin Exp Pathol 2019;12(11):4087-4095.  WB&IHC-P ;  Mouse.  
        [IF=3.471] Chen J et al. Modulation of activated astrocytes in the hypothalamus paraventricular nucleus to prevent ventricular arrhythmia complicating acute myocardial infarction. Int J Cardiol. 2020 Jan 16.  WB&IHC-P ;  Rat.  
        研究领域 肿瘤  细胞生物  免疫学  神经生物学  信号转导  干细胞  细胞粘附分子  细胞类型标志物  细胞骨架  
        抗体来源 Rabbit
        克隆类型 Polyclonal
        交叉反应 Human, Mouse, Rat,  (predicted: Dog, Pig, Cow, Rabbit, Sheep, )
        产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:200-1000 IHC-F=1:200-1000 Flow-Cyt=1μg/Test ICC=1:100 IF=1:200-800 (石蜡切片需做抗原修复)
        not yet tested in other applications.
        optimal dilutions/concentrations should be determined by the end user.
        分 子 量 48kDa
        细胞定位 细胞浆 
        性    状 Liquid
        浓    度 1mg/ml
        免 疫 原 KLH conjugated Synthesised phosphopeptide derived from human GFAP around the phosphorylation site of Ser8:51-150/432 
        亚    型 IgG
        纯化方法 affinity purified by Protein A
        储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
        保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
        PubMed PubMed
        产品介绍 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. [provided by RefSeq, Oct 2008]

        Function:
        GFAP, a class-III intermediate filament, is a cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells.

        Subunit:
        Interacts with SYNM. Isoform 3 interacts with PSEN1 (via N-terminus).

        Subcellular Location:
        Cytoplasm. Note=Associated with intermediate filaments.

        Tissue Specificity:
        Expressed in cells lacking fibronectin.

        Post-translational modifications:
        Phosphorylated by PKN1.

        DISEASE:
        Defects in GFAP are a cause of Alexander disease (ALEXD) [MIM:203450]. Alexander disease is a rare disorder of the central nervous system. It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes. The most common form affects infants and young children, and is characterized by progressive failure of central myelination, usually leading to death usually within the first decade. Infants with Alexander disease develop a leukoencephalopathy with macrocephaly, seizures, and psychomotor retardation. Patients with juvenile or adult forms typically experience ataxia, bulbar signs and spasticity, and a more slowly progressive course.

        Similarity:
        Belongs to the intermediate filament family.

        SWISS:
        P14136

        Gene ID:
        2670

        Database links:

        Entrez Gene: 281189 Cow

        Entrez Gene: 2670 Human

        Entrez Gene: 14580 Mouse

        Entrez Gene: 24387 Rat

        Omim: 137780 Human

        SwissProt: Q28115 Cow

        SwissProt: P14136 Human

        SwissProt: P03995 Mouse



        Important Note:
        This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

        星形胶质细胞标志物 (Astrocyte Marker)

        GFAP是一个56kDa的中间丝蛋白(intermediate filament,IF),在中枢神经系统发育期是一个特异性的标志物,以区别星形细胞和其它胶质细胞。GFAP表达在皮层和海马,急、慢性皮质酮治疗时表达减少。
        GFAP可以和人、大鼠、小鼠的GFAP反应,在正常和肿瘤性的星形胶质细胞阳性表达,而神经节细胞、神经元、成纤维细胞、少突胶质细胞和这些细胞来源的肿瘤细胞阴性表达,主要用于星形胶质瘤等中枢神经系统肿瘤的诊断和鉴别诊断,GFAP的缺乏可导致AD病。
        产品图片
        Sample:Optic nerve (Rat)cell Lysate at 40 ug
        Primary: Anti-GFAP(bs-0199R)at 1/300 dilution
        Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution
        Predicted band size: 48 kD
        Observed band size: 53 kD
        Sample: U251 Cell Lysate at 40 ug
        Primary: Anti- GFAP (bs-0199R) at 1/300 dilution
        Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/10000 dilution
        Predicted band size: 48 kD
        Observed band size: 50 kD
        Sample:
        Cerebellum (Rat) Lysate at 40 ug
        Cerebellum (Mouse) Lysate at 40 ug
        Eye (Mouse) Lysate at 40 ug
        Primary: Anti-GFAP (bs-0199R) at 1/300 dilution
        Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
        Predicted band size: 48 kD
        Observed band size: 48 kD
        Tissue/cell: rat brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
        Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
        Incubation: Anti-GFAP Polyclonal Antibody, Unconjugated(bs-0199R) 1:400, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
        Paraformaldehyde-fixed, paraffin embedded (mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
        Paraformaldehyde-fixed, paraffin embedded (mouse cerebellum); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
        Paraformaldehyde-fixed, paraffin embedded (rat cerebellum); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
        Paraformaldehyde-fixed, paraffin embedded (mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
        Paraformaldehyde-fixed, paraffin embedded (rat brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
        Paraformaldehyde-fixed, paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
        Tissue/cell: rat brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
        Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
        Incubation: Anti-GFAP Polyclonal Antibody, Unconjugated(bs-0199R) 1:500, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
        Tissue/cell:U-251 cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (GFAP) polyclonal Antibody, Unconjugated (bs-0199R) 1:100, 90 minutes at 37°C; followed by a FITC conjugated Goat Anti-Rabbit IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.
        Paraformaldehyde-fixed, paraffin embedded (Human brain glioma); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:400 overnight at 4°C, followed by a conjugated Goat Anti-Rabbit IgG antibody (bs-0295G-FITC) for 90 minutes, and DAPI for nuclei staining.
        Paraformaldehyde-fixed, paraffin embedded (rat brain); Antigen retrieval by boiling in sodium citrate buffer (pH6) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GFAP) Polyclonal Antibody, Unconjugated (bs-0199R) at 1:200 overnight at 4°C, followed by a conjugated secondary (bs-0295G-Cy3) at [1:500] for 90 minutes and DAPI staining of the nuclei.
        Tissue/cell: rat brain tissue;4% Paraformaldehyde-fixed and paraffin-embedded;
        Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
        Incubation: Anti-GFAP Polyclonal Antibody, Unconjugated(bs-0199R) 1:400, overnight at 4°C; The secondary antibody was Goat Anti-Rabbit IgG, Cy3 conjugated(bs-0295G-Cy3)used at 1:200 dilution for 40 minutes at 37°C. DAPI(5ug/ml,blue,C-0033) was used to stain the cell nuclei
        Blank control: RSC96(blue).
        Primary Antibody:Rabbit Anti- GFAP antibody(bs-0199R), Dilution: 1μg in 100 μL 1X PBS containing 0.5% BSA;
        Isotype Control Antibody: Rabbit IgG(orange) ,used under the same conditions );
        Secondary Antibody: Goat anti-rabbit IgG-PE(white blue), Dilution: 1:200 in 1 X PBS containing 0.5% BSA.
        Protocol
        The cells were fixed with 2% paraformaldehyde (10 min) , then permeabilized with 90% ice-cold methanol for 30 min on ice. Primary antibody (bs-0199R, 1μg /1x10^6 cells) were incubated for 30 min on the ice, followed by 1 X PBS containing 0.5% BSA + 1 0% goat serum (15 min) to block non-specific protein-protein interactions. Then the Goat Anti-rabbit IgG/PE antibody was added into the blocking buffer mentioned above to react with the primary antibody at 1/200 dilution for 30 min on ice. Acquisition of 20,000 events was performed.
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