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KD-Validated EEF1A2 Recombinant Rabbit mAb

#65671

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using EEF1A2 antibody (Cat#65671). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with EEF1A2 antibody (Cat#65671, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using EEF1A2 antibody (Cat#65671). EEF1A2 expression in wild-type (WT) and EEF1A2 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with EEF1A2 antibody (Cat#65671, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HACAT cells with EEF1A2 antibody (Cat#65671, 1:1,000). Nuclei were stained blue with DAPI; EEF1A2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Flow cytometric analysis of EEF1A2 expression in HaCaT cells using EEF1A2 antibody (Cat#65671,1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, EEF1A2.
Validation of EEF1A2 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with EEF1A2 antibody (Cat#65671, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
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  • Gene Symbol:
    EEF1A2
  • Catalog:
    65671
  • Application:
    WB, FCM, ICC
  • Species Reactivity:
    H
Information
Product Name KD-Validated EEF1A2 Recombinant Rabbit mAb
Aliases EEF1A2; Eukaryotic Translation Elongation Factor 1 Alpha 2; EEF1AL; HS1; STN; Eukaryotic Elongation Factor 1 A-2; Elongation Factor 1-Alpha 2; EF-1-Alpha-2; Statin-S1; STNL; Statin-Like; EEF1A-2; Statin; EIEE33; DEE33; MRD38; EF1A
Background

Gene Name: EEF1A2

NCBI Gene Entry: 1917

UniProt Entry: Q05639

Application Information

Molecular Weight: Predicted, 50 kDa; observed, 48-50 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 25GB4655

Species Reactivity: Human

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC)

Immunogen A synthesized peptide derived from human EEF1A2
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:1,000-1:5,000
Flow Cytometry (FCM): 1:200-1:2,000
Immunocytochemistry (ICC): 1:100-1:1,000
Note This product is for research use only.
Data
  • Western blotting analysis using EEF1A2 antibody (Cat#65671). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with EEF1A2 antibody (Cat#65671, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Western blotting analysis using EEF1A2 antibody (Cat#65671). EEF1A2 expression in wild-type (WT) and EEF1A2 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with EEF1A2 antibody (Cat#65671, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Immunocytochemical staining of HACAT cells with EEF1A2 antibody (Cat#65671, 1:1,000). Nuclei were stained blue with DAPI; EEF1A2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
  • Flow cytometric analysis of EEF1A2 expression in HaCaT cells using EEF1A2 antibody (Cat#65671,1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, EEF1A2.
  • Validation of EEF1A2 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with EEF1A2 antibody (Cat#65671, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
Western blotting analysis using EEF1A2 antibody (Cat#65671). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with EEF1A2 antibody (Cat#65671, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using EEF1A2 antibody (Cat#65671). EEF1A2 expression in wild-type (WT) and EEF1A2 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with EEF1A2 antibody (Cat#65671, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HACAT cells with EEF1A2 antibody (Cat#65671, 1:1,000). Nuclei were stained blue with DAPI; EEF1A2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Flow cytometric analysis of EEF1A2 expression in HaCaT cells using EEF1A2 antibody (Cat#65671,1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, EEF1A2.
Validation of EEF1A2 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with EEF1A2 antibody (Cat#65671, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
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