货号：04-1062

品牌：Merck Millipore

规格：

目录价：￥4505.00

市场价格：￥3829.25

会员价格：￥3604.00

金山科研平台，产品价格货期咨询微信：jinshanbio Description: Anti-GFAP (N-term) Antibody, clone EPR1034Y, Rabbit | 04-1062 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Specificity: This antibody recognizes GFAP at and around the N-terminus. View All» Molecular Weight: ~50 kDa View All» Epitope: N-terminus View All» Immunogen: Synthetic peptide corresponding to residues in the N-terminus of human GFAP. View All» Clone: EPR1034Y View All» Isotype: IgG View All» Background Information: Glial fibrillary acidic protein is a class-III intermediate filament. GFAP is the main constituent of intermediate filaments in astrocytes and serves as a cell specific marker that distinguishes differentiated astrocytes from other glial cells during the development of the central nervous system. View All» Species Reactivity:

• Human

• Mouse

• Rat
  View All» Species Reactivity Note: Human, mouse, and rat. View All» Application Notes: Immunohistochemistry Analysis: A 1:250-500 dilution from a previous lot detected GFAP in human brain and human glioma tissue.Immunocytochemistry Analysis: A 1:100-250 dilution from a previous lot was used in IC.Immunoprecipitation Analysis: A 1:40 dilution from a previous lot was used in IP. View All» Control: Human and Rat brain lysates View All» Quality Assurance: Evaluated by Western Blot on Human and Rat brain cell lysates.Western Blot Analysis: 1:50,000-100,000 dilution of this antibody was used to detect GFAP in human and rat brain cell lysates. View All» Purification Method: Unpurified View All» Presentation: Rabbit Monoclonal in buffer containing 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl containing 40% Glycerol, 0.01% sodium azide and 0.05% BSA. View All» Storage Conditions: Stable for 1 year at -20ºC from date of receipt.Handling Recommendations: Upon first thaw, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance. Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage. View All» UniProt Number: P14136 View All» Entrez Gene Number: NP_001124491.1 View All» Gene Symbol: FLJ45472 View All» Alternate Names: glial fibrillary acidic protein View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications:
  • Western Blotting

  • Immunohistochemistry (Paraffin)

  • Immunocytochemistry

  • Immunoprecipitation
    View All» Entrez Gene Summary: 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. View All» UniProt Summary: 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 STRUCTURE: Interacts with SYNM By similarity. Isoform 3 interacts with PSEN1 (via N-terminus).SUBCELLULAR LOCATION: Cytoplasm. Note: Associated with intermediate filaments.TISSUE SPECIFICITY: Expressed in cells lacking fibronectin. INVOLVEMENT IN 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. SEQUENCE SIMILARITIES: Belongs to the intermediate filament family. View All» Product Name: Anti-GFAP (N-term), clone EPR1034Y, Rabbit Monoclonal View All» Antibody Type: Monoclonal Antibody View All» Qty/Pk: 100 µL View All» Format: Unpurified View All» Host: Rabbit View All»
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