tcba166 GFAP Polyclonal Antibody

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Product Description

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.

Information

ApplicationWB, IHC, IF
Research AreaStem cells, Neural Stem Cells, Neuroscience,
Species ReactivityHuman, Mouse, Rat
Host SpeciesRabbit
IsotypeIgG

Specifications

FormLiquid
Storage BufferBuffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Recommended DilutionWB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:50 - 1:200

Misc Information

Storage InstructionStore at -20℃. Avoid freeze / thaw cycles.
Alternative NamesALXDRD
SwissProtP14136
Gene ID2670 (human);
Calculated Molecular Weight49kDa/50kDa
PurificationAffinity purification
Cellular LocationCytoplasm,
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