AKT1 Mouse Monoclonal Antibody [D9-9-C9]
cat.: EM40507
Product Type: Mouse monoclonal IgG2b, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P, FC
Clonality: Monoclonal
Clone number: D9-9-C9
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 56 kDa
Isotype: IgG2b
Immunogen: Synthetic peptide within human AKT1 aa 1-80.
Positive control: MCF7 cell lysate, A549 cell lysate, Jurkat cell lysate, C2C12 cell lysate, L-929 cell lysate, C6 cell lysate, Hela, HepG2, MCF-7, human breast carcinoma tissue.
Subcellular location: Nucleus, cytoplasm, cell membrane.
Recommended Dilutions:
  WB
  IHC-P
  IF-Cell
  FC

1:2,000
1:100-1:200
1:100-1:200
1:100-1:200
Uniprot #: SwissProt: P31749 Human | P31750 Mouse | P47196 Rat
Alternative names: AKT 1 AKT AKT1 AKT1_HUMAN MGC99656 PKB PKB-ALPHA PRKBA Protein Kinase B Alpha Protein kinase B Proto-oncogene c-Akt RAC Alpha RAC RAC-alpha serine/threonine-protein kinase RAC-PK-alpha
Images
EM40507_1.jpg Fig1: Western blot analysis of AKT1 on different lysates with Mouse anti-AKT1 antibody (EM40507) at 1/2,000 dilution.

Lane 1: MCF7 cell lysate
Lane 2: A549 cell lysate
Lane 3: Jurkat cell lysate
Lane 4: C2C12 cell lysate
Lane 5: L-929 cell lysate
Lane 6: C6 cell lysate

Lysates/proteins at 15 µg/Lane.

Predicted band size: 56 kDa
Observed band size: 56 kDa

Exposure time: 30 seconds;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (EM40507) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/50,000 dilution was used for 1 hour at room temperature.
EM40507_2.jpg Fig2: ICC staining Akt1 in Hela cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM40507_3.jpg Fig3: ICC staining Akt1 in HepG2 cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM40507_4.jpg Fig4: ICC staining Akt1 in MCF-7 cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
EM40507_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-Akt1 antibody. Counter stained with hematoxylin.
EM40507_6.jpg Fig6: Flow cytometric analysis of Hela cells with Akt1 antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti mouse IgG (FITC) was used as the secondary antibody.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.