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MAB5628 Anti-Glial Fibrillary Acidic Protein Antibody

Detect Glial Fibrillary Acidic Protein using this Anti-Glial Fibrillary Acidic Protein Antibody validated for use in WB & IC.

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
Research Category: Neuroscience Research Sub-Category: Neuronal & Glial Markers Gene Symbol: GFAP, FLJ45472 UniProt Number: P14136
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MAB5628
100 µg  
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      Overview

      Replacement Information

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      Key Spec Table

      Species ReactivityKey ApplicationsHostFormatAntibody Type
      H, RWB, ICCMPurifiedMonoclonal Antibody
      Description
      Catalogue NumberMAB5628
      Replaces04-1031; 04-1062
      Brand Family Chemicon®
      Trade Name
      • Chemicon
      DescriptionAnti-Glial Fibrillary Acidic Protein Antibody
      Alternate Names
      • GFAP
      References
      Product Information
      FormatPurified
      Control
      • Positive: Neural tissue or astrocyte culture
        Negative: Non-neural tissue or neuronal culture
      PresentationPurified immunoglobulin. Liquid in 0.02M phosphate buffer, 0.25 M NaCl, pH 7.6 with 0.1% sodium azide.
      Quality LevelMQ100
      Applications
      ApplicationDetect Glial Fibrillary Acidic Protein using this Anti-Glial Fibrillary Acidic Protein Antibody validated for use in WB & IC.
      Key Applications
      • Western Blotting
      • Immunocytochemistry
      Application NotesWestern blot: 1:10,000 on rat brain

      Optimal working dilutions must be determined by end user.
      Biological Information
      ConcentrationPlease refer to the Certificate of Analysis for the lot-specific concentration.
      HostMouse
      IsotypeIgG2a
      Species Reactivity
      • Human
      • Rat
      Antibody TypeMonoclonal Antibody
      Entrez Gene Number
      Entrez Gene SummaryThis 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. An additional transcript variant has been described, but its full length sequence has not been determined.
      Gene Symbol
      • GFAP
      • FLJ45472
      UniProt Number
      UniProt SummaryFUNCTION: SwissProt: P14136 # 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.
      SIZE: 432 amino acids; 49880 Da
      SUBUNIT: Isoform 3 interacts with N-terminus of PSEN1.
      SUBCELLULAR LOCATION: Cytoplasm. Note=Associated with intermediate filaments.
      DISEASE: SwissProt: P14136 # Defects in GFAP are a cause of Alexander disease [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: SwissProt: P14136 ## Belongs to the intermediate filament family.
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      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.
      Storage and Shipping Information
      Storage ConditionsMaintain at 2-8°C in undiluted aliquots for up to 6 months after date of receipt.
      Packaging Information
      Material Size100 µg
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Catalogue Number GTIN
      MAB5628 04053252727436

      Documentation

      Anti-Glial Fibrillary Acidic Protein Antibody SDS

      Title

      Safety Data Sheet (SDS) 

      Anti-Glial Fibrillary Acidic Protein Antibody Certificates of Analysis

      TitleLot Number
      MOUSE ANTI-GFAP - 3247093 3247093
      MOUSE ANTI-GFAP - 3384532 3384532
      MOUSE ANTI-GFAP - 3718411 3718411
      MOUSE ANTI-GFAP - 4095071 4095071
      MOUSE ANTI-GFAP - 4224997 4224997
      MOUSE ANTI-GFAP MONOCLONAL ANTIBODY 2937334
      MOUSE ANTI-GFAP MONOCLONAL ANTIBODY 2953778
      MOUSE ANTI-GFAP MONOCLONAL ANTIBODY 2882024
      MOUSE ANTI-GFAP MONOCLONAL ANTIBODY - 2123142 2123142
      MOUSE ANTI-GFAP MONOCLONAL ANTIBODY - 2420476 2420476
      Show more

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      Product Families

      Glial Cell Markers

      Glial cells, sometimes called neuroglia are non-neuronal cells that maintain homeostasis, form myelin, and provide support and protection for neurons in the brain and peripheral nervous system.
      Learn More >>

      GFAP Antibodies & Kits

      Millipore’s GFAP antibodies demonstrate specificity against Glial Fibrillary Acidic Protein (GFAP). See below for related products for GFAP, based on the expertise of Upstate & Chemicon.
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      Categories

      Life Science Research > Antibodies and Assays > Primary Antibodies