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ARP2 Antibody

Catalog Number: orb340961

Select Product Size
SizePriceQuantity
30 μl$ 120.00
50 μl$ 160.00
100 μl$ 240.00
200 μl$ 340.00
30 μl Enquire
50 μl Enquire
100 μl Enquire
200 μl Enquire
DispatchUsually dispatched within 5-10 working days
Catalog Numberorb340961
CategoryAntibodies
DescriptionRabbit polyclonal antibody to ACTR2
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 ARP2
UniProt IDQ5M7U6, P61160, P61161
Tested applicationsIF, IHC, WB
Dilution rangeWB: 1:500-1:2000, IHC-P: 1:50-1:200
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 namesARP2; Actin-related protein 2; Actin-like protein
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Research AreaEpigenetics
NoteFor research use only
Entrez66713, 289820, 10097
Expiration Date12 months from date of receipt.
ARP2 Antibody

Western blot analysis of ARP2 expression in HepG2 (A), Hela (B), mouse lung (C), mouse brain (D) whole cell lysates. (Predicted band size: 44; 45 kD; Observed band size: 45 kD)

ARP2 Antibody

Immunohistochemical analysis of ARP2 staining in human liver 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.

ARP2 Antibody

Immunofluorescent analysis of ARP2 staining in U2OS 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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