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KD-Validated Anti-Cyclin A1/A2 Rabbit Monoclonal Antibody #61382

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Flow cytometric analysis of Cyclin A1/A2 expression in HAP-1 cells using Cyclin A1/A2 antibody (Cat#61382, 1:2,000). Green, isotype control; red, Cyclin A1/A2.
Immunocytochemical staining of HAP-1 cells with Cyclin A1/A2 antibody (Cat#61382, 1:1,000). Nuclei were stained blue with DAPI; Cyclin A1/A2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar: 20 μm.
Western blotting analysis using anti-Cyclin A1/A2 antibody (Cat#61382). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Cyclin A1/A2 antibody (Cat#61382, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-Cyclin A1 antibody (Cat#61382). Cyclin A1 expression in wild type (WT) and Cyclin A1 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-Cyclin A1 antibody (Cat#61382, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • 基因名:
    CCNA1/2
  • 货号:
    61382
  • 应用:
    WB, FCM, IC
  • 物种反应性:
    H, M, R
规格:
20 μL,50 μL,100 μL
价格:
¥ 650.00,¥ 1,350.00,¥ 2,500.00
Information
Product Name KD-Validated Anti-Cyclin A1/A2 Rabbit Monoclonal Antibody
Aliases CCNA2; Cyclin A2; CCN1; CCNA; Cyclin-A2; Cyclin-A; Cyclin A; CCNA1; Cyclin A1; CT146; Cyclin-A1; Testicular Tissue Protein Li 34
Background

Gene Name: CCNA1/2

NCBI Gene Entry: 890/8900

UniProt Entry: P20248/ P78396

Application Information

Molecular Weight: Predicted, 52 kDa, observed, 52 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB3525

Species Reactivity: Human, mouse, rat

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

Immunogen A synthesized peptide derived from human Cyclin A1/A2
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): 1:2,000
Immunocytochemistry (IC): 1:100-1:1,000
Note This product is for research use only.
Picture
  • Flow cytometric analysis of Cyclin A1/A2 expression in HAP-1 cells using Cyclin A1/A2 antibody (Cat#61382, 1:2,000). Green, isotype control; red, Cyclin A1/A2.
  • Immunocytochemical staining of HAP-1 cells with Cyclin A1/A2 antibody (Cat#61382, 1:1,000). Nuclei were stained blue with DAPI; Cyclin A1/A2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar: 20 μm.
  • Western blotting analysis using anti-Cyclin A1/A2 antibody (Cat#61382). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Cyclin A1/A2 antibody (Cat#61382, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using anti-Cyclin A1 antibody (Cat#61382). Cyclin A1 expression in wild type (WT) and Cyclin A1 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-Cyclin A1 antibody (Cat#61382, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Citation(0)
Flow cytometric analysis of Cyclin A1/A2 expression in HAP-1 cells using Cyclin A1/A2 antibody (Cat#61382, 1:2,000). Green, isotype control; red, Cyclin A1/A2.
Immunocytochemical staining of HAP-1 cells with Cyclin A1/A2 antibody (Cat#61382, 1:1,000). Nuclei were stained blue with DAPI; Cyclin A1/A2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar: 20 μm.
Western blotting analysis using anti-Cyclin A1/A2 antibody (Cat#61382). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Cyclin A1/A2 antibody (Cat#61382, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-Cyclin A1 antibody (Cat#61382). Cyclin A1 expression in wild type (WT) and Cyclin A1 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-Cyclin A1 antibody (Cat#61382, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
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