GFAP monoclonal antibody, clone ECO-7
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More Files
- More Functions
Western Blot (Cell lysate)
Western Blot analysis of rat brain tissue lysate with GFAP monoclonal antibody, clone ECO-7 (Cat # MAB20086).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human glioma with GFAP monoclonal antibody, clone ECO-7 (Cat # MAB20086).
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Specification
Product Description
Rabbit monoclonal antibody raised against synthetic peptide of human GFAP.
Immunogen
A synthetic peptide corresponding to human GFAP.
Host
Rabbit
Theoretical MW (kDa)
49.88
Reactivity
Human
Form
Liquid
Purification
Affinity purification
Isotype
IgG
Recommend Usage
Immunocytochemistry (1:50-1:200)
Immunofluorescence (1:50-1:200)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:50-1:200)
Western Blot (1:500-1:2000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, 150 mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide).
Storage Instruction
Store at -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.
Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western Blot analysis of rat brain tissue lysate with GFAP monoclonal antibody, clone ECO-7 (Cat # MAB20086).Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human glioma with GFAP monoclonal antibody, clone ECO-7 (Cat # MAB20086).Immunocytochemistry
Immunofluorescence
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Gene Info — GFAP
Entrez GeneID
2670Protein Accession#
P14136Gene Name
GFAP
Gene Alias
FLJ45472
Gene Description
glial fibrillary acidic protein
Gene Ontology
HyperlinkGene 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. [provided by RefSeq
Other Designations
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Interactome
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Disease
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