Merck Millipore代理AG230 Glial Fibrillary Acidic Protein, porcine;store at -20℃

2025-07-24

货号:AG230

品牌:Merck Millipore

规格:100Ug

目录价:¥3377.00

市场价格:¥2870.45

会员价格:¥2701.60

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Glial Fibrillary Acidic Protein, porcine View All» Trade Name: Chemicon (Millipore) View All» Qty/Pk: 100 µg View All» Product Overview: Purified porcine Glial Fibrillary Acidic Protein (GFAP) purified from spinal cord. View All» Key Applications:

  • Western Blotting

  • ELISA

  • Radioimmunoassay

    View All» Application Notes: Western blotting Protein standard ELISA Radioimmunoassay Optimal working dilution must be determined by the end user. 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» 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. An additional transcript variant has been described, but its full length sequence has not been determined. View All» UniProt Summary: FUNCTION: 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. View All» Species: Porcine View All» Brand Family: Chemicon View All» Presentation: Liquid. Buffer = PBS. View All» UniProt Number: P14136 View All» Storage Conditions: Maintain at -20°C to -70°C in undiluted aliquots for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles. During shipment, small volumes of product will occasionally become entrapped in the seal of the product vial. For products with volumes of 200 μL or less, we recommend gently tapping the vial on a hard surface or briefly centrifuging the vial in a tabletop centrifuge to dislodge any liquid in the container's cap. View All» Promotional Text: Special Offer on Antibodies! Click Here! View All» Gene Symbol:
    • GFAP

    • FLJ45472

      View All» Product Name: Glial Fibrillary Acidic Protein, porcine View All» Entrez Gene Number: NM_002055.2 View All» Alternate Names: GFAP View All» Concentration: ~330 μg/mL View All» Purity: Contains >98% pure GFAP, a 50 kDa single band by SDS-PAGE. View All»

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