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GFAP Antibody

On Promotion

Catalog Number: orb1473999

Select Product Size
SizePriceQuantity
30 μl$ 120.00
50 μl$ 160.00
100 μl$ 240.00
200 μl$ 340.00
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DispatchUsually dispatched within 5-10 working days
Product Properties
Catalog Numberorb1473999
CategoryAntibodies
DescriptionThe GFAP Antibody is suitable for IF, IHC, WB. It is a Monoclonal, Unconjugated antibody which raised against Recombinant fusion protein of human GFAP. The exact sequence is proprietary. Purification: This antibody is purified through a protein G column.
ClonalityMonoclonal
Species/HostMouse
ConjugationUnconjugated
ReactivityHuman
Form/AppearanceMouse IgG2b kappa. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide.
PurificationThis antibody is purified through a protein G column.
ImmunogenRecombinant fusion protein of human GFAP. The exact sequence is proprietary.
UniProt IDP14136
Tested applicationsIF, IHC, WB
Dilution rangeWB (1/500 - 1/2000), IH (1/100 - 1/400), IF/IC (1/10 - 1/50)
Antibody TypePrimary Antibody
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Alternative namesGlial fibrillary acidic protein; GFAP
NoteFor research use only
Entrez2670
Images
GFAP Antibody

Western blot analysis of GFAP expression in human brain (A), human cerebellum (B) whole cell lysates. (Predicted band size: 49 kD; Observed band size: 45-50 kD)

GFAP Antibody

Immunohistochemical analysis of GFAP staining in human brain formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

GFAP Antibody

Immunofluorescent analysis of GFAP staining in brain tissue cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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