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Anti-AKT2 Antibody

Catalog Number: orb213546

DispatchUsually dispatched within 5-10 working days
$ 140.00
Catalog Numberorb213546
CategoryAntibodies
DescriptionRabbit polyclonal antibody to AKT2
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsIF, IH, WB
ReactivityHuman, Mouse, Rat
ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human AKT2. The exact sequence is proprietary.
Antibody TypePrimary Antibody
Dilution rangeWB: 1-500-1-1000, IHC-P: 1-100-1-200, IF/ICC: 1-100-1-500
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
ConjugationUnconjugated
TargetAKT2
Entrez11652, 208, 25233
UniProt IDP31751, Q60823, P47197
SourceRabbit
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.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Alternative namesanti RAC-beta serine/threonine-protein kinase anti
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NoteFor research use only
Expiration Date12 months from date of receipt.
Anti-AKT2 Antibody

Western blot analysis of AKT2 expression in A549 (A), LO2 (B), AML12 (C), C6 (D) whole cell lysates. (Predicted band size: 55 kD; Observed band size: 60 kD)

Anti-AKT2 Antibody

Immunohistochemical analysis of AKT2 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.

Anti-AKT2 Antibody

Immunofluorescent analysis of AKT2 staining in HepG2 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 DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.

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    10 μg, 100 μg
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    ELISA,  IF,  IHC-P,  WB

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