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    Mouse Anti-GFAP  antibody (bsm-33065M)  
    ~~~促銷(xiāo)代碼KT202411~~~
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    產(chǎn)品編號 bsm-33065M
    英文名稱(chēng) Mouse Anti-GFAP  antibody
    中文名稱(chēng) 膠質(zhì)纖維酸性蛋白單克隆抗體
    別    名 Astrocyte; FLJ45472; GFAP; Glial Fibrillary Acidic Protein; Intermediate filament protein; GFAP_HUMAN.  
    Specific References  (1)     |     bsm-33065M has been referenced in 1 publications.
    [IF=3.046] Yukari Nagakura. et al. Expression of nischarin, an imidazoline 1 receptor candidate protein, in the ventrolateral medulla of newborn rats. Neurosci Lett. 2021 Jul;:136113  IHC ;  Rat.  
    研究領(lǐng)域 腫瘤  細胞生物  神經(jīng)生物學(xué)  
    抗體來(lái)源 Mouse
    克隆類(lèi)型 Monoclonal
    克 隆 號 7D8
    交叉反應 Human,Mouse,Rat
    產(chǎn)品應用 WB=1:500-1000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 49kDa
    細胞定位 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 Recombinant mouse GFAP full length 
    亞    型 IgG
    純化方法 affinity purified by Protein G
    緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產(chǎn)品介紹 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



    星形膠質(zhì)細胞標志物 (Astrocyte Marker)
    GFAP是一個(gè)56kDa的中間絲蛋白(intermediate filament,IF),在中樞神經(jīng)系統發(fā)育期是一個(gè)特異性的標志物,以區別星形細胞和其它膠質(zhì)細胞。GFAP表達在皮層和海馬,急、慢性皮質(zhì)酮治療時(shí)表達減少。
    GFAP可以和人、大鼠、小鼠的GFAP反應,在正常和腫瘤性的星形膠質(zhì)細胞陽(yáng)性表達,而神經(jīng)節細胞、神經(jīng)元、成纖維細胞、少突膠質(zhì)細胞和這些細胞來(lái)源的腫瘤細胞陰性表達,主要用于星形膠質(zhì)瘤等中樞神經(jīng)系統腫瘤的診斷和鑒別診斷,GFAP的缺乏可導致AD病。
    產(chǎn)品圖片
    Sample: Cerebellum (Mouse) Lysate at 40 ug Primary: Anti- GFAP (bsm-33065M) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kD Observed band size: 50 kD
    Sample: Cerebrum (Mouse) Lysate at 40 ug Spinal cord (Mouse) Lysate at 40 ug Primary: Anti- TBX1 (bsm-33065M) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 50 kD Observed band size: 50 kD
    Sample: mouse brain Lysate at 25 ug Primary: Mouse Anti-GFAP(bsm-33065M) at 1/500 dilution Secondary: IRDye800CW Goat Anti-Mouse IgG at 1/20000 dilution Predicted band size: 49kD Observed band size: 49kD
    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) Monoclonal Antibody, Unconjugated (bsm-33065M) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Mouse) (sp-0024) instructionsand DAB staining.
    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) Monoclonal Antibody, Unconjugated (bsm-33065M) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Mouse)(sp-0024) 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) Monoclonal Antibody, Unconjugated (bsm-33065M) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Mouse)(sp-0024) instructionsand DAB staining.
    Tissue/cell: BV-2 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) Monoclonal Antibody, Unconjugated (bsm-33065M) 1:50, 90 minutes at 37°C; followed by a conjugated Goat Anti-Mouse IgG antibody (bs-0296G-FITC) at 37°C for 90 minutes, DAPI (5ug/ml, blue, C-0033) was used to stain the cell nuclei.
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