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S100-A4 Antibody

Catalog Number: orb382023

Select Product Size
SizePriceQuantity
30 μl$ 120.00
50 μl$ 160.00
100 μl$ 240.00
200 μl$ 340.00
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50 μl Enquire
100 μl Enquire
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DispatchUsually dispatched within 5-10 working days
Catalog Numberorb382023
CategoryAntibodies
DescriptionRabbit polyclonal antibody to S100A4.
ClonalityPolyclonal
Species/HostRabbit
ConjugationUnconjugated
ReactivityHuman, Mouse, Rat
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
PurificationThe antibody was purified by immunogen affinity chromatography.
ImmunogenRecombinant fusion protein of human S100-A4
UniProt IDP05942, P26447, P07091
Tested applicationsIF, IHC, WB
Dilution rangeWB: 1:500-2000, IHC-P: 1:50-200
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 namesCAPL; MTS1; Protein S100-A4; Calvasculin; Metastas
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Research AreaEpigenetics
NoteFor research use only
Entrez6275, 20198, 24615
Expiration Date12 months from date of receipt.
S100-A4 Antibody

Western blot analysis of S100-A4 expression in Hela (A), NIH3T3 (B), HepG2 (C) whole cell lysates. (Predicted band size: 11 kD; Observed band size: 12 kD)

S100-A4 Antibody

Immunohistochemical analysis of S100-A4 staining in human breast cancer 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.

S100-A4 Antibody

Immunofluorescent analysis of S100-A4 staining in Raw264.7 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 AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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