• 一抗
  • 二抗
  • 慢病毒
  • 细胞系
  • 裂解物
  • 试剂类

KD-Validated Anti-TFAP2A Rabbit Monoclonal Antibody #62671

一键复制产品信息
Flow cytometric analysis of TFAP2A expression in HepG2 cells using anti-TFAP2A antibody (Cat#62671, 1:2,000). Green, isotype control; red, TFAP2A.
Immunocytochemical staining of HepG2 cells with anti-TFAP2A antibody (Cat#62671, 1:1,000). Nuclei were stained blue with DAPI; TFAP2A 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-TFAP2A antibody (Cat#62671). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TFAP2A antibody (Cat#62671, 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-TFAP2A antibody (Cat#62671). TFAP2A expression in wild type (WT) and TFAP2A shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-TFAP2A antibody (Cat#62671, 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).
Immunohistochemistry was performed on paraffin-embedded human breast carcinoma using anti-glial fibrillary acidic protein antibody (Cat#62671, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • 基因名:
    TFAP2A
  • 货号:
    62671
  • 应用:
    WB, FCM, IC, IHC
  • 物种反应性:
    H, 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-TFAP2A Rabbit Monoclonal Antibody
Aliases TFAP2A; Transcription Factor AP-2 Alpha; AP-2; AP-2alpha; AP2TF; TFAP2; Transcription Factor AP-2 Alpha (Activating Enhancer Binding Protein 2 Alpha); Activating Enhancer-Binding Protein 2-Alpha; Transcription Factor AP-2-Alpha; AP-2 Transcription Factor; Activator Protein 2; Transcription Factor AP-2 Alpha (Activating Enhancer-Binding Protein 2 Alpha); AP2-Alpha; BOFS
Background

Gene Name: TFAP2A

NCBI Gene Entry: 7020

UniProt Entry: P05549

Application Information

Molecular Weight: Predicted, 48 kDa, observed, 48 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB2485

Species Reactivity: Human, rat

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

Immunogen A synthesized peptide derived from human AP2 alpha
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
Immunohistochemistry (IHC): 1:100-1:200
Note This product is for research use only.
Picture
  • Flow cytometric analysis of TFAP2A expression in HepG2 cells using anti-TFAP2A antibody (Cat#62671, 1:2,000). Green, isotype control; red, TFAP2A.
  • Immunocytochemical staining of HepG2 cells with anti-TFAP2A antibody (Cat#62671, 1:1,000). Nuclei were stained blue with DAPI; TFAP2A 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-TFAP2A antibody (Cat#62671). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TFAP2A antibody (Cat#62671, 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-TFAP2A antibody (Cat#62671). TFAP2A expression in wild type (WT) and TFAP2A shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-TFAP2A antibody (Cat#62671, 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).
  • Immunohistochemistry was performed on paraffin-embedded human breast carcinoma using anti-glial fibrillary acidic protein antibody (Cat#62671, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Citation(0)
Flow cytometric analysis of TFAP2A expression in HepG2 cells using anti-TFAP2A antibody (Cat#62671, 1:2,000). Green, isotype control; red, TFAP2A.
Immunocytochemical staining of HepG2 cells with anti-TFAP2A antibody (Cat#62671, 1:1,000). Nuclei were stained blue with DAPI; TFAP2A 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-TFAP2A antibody (Cat#62671). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TFAP2A antibody (Cat#62671, 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-TFAP2A antibody (Cat#62671). TFAP2A expression in wild type (WT) and TFAP2A shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-TFAP2A antibody (Cat#62671, 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).
Immunohistochemistry was performed on paraffin-embedded human breast carcinoma using anti-glial fibrillary acidic protein antibody (Cat#62671, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • 联系电话

    0551-63635518

    0551-65578998

  • 联系邮箱

    support@genuinbiotech.cn

    sales@genuinbiotech.cn

微信公众号

Copyright © 2025 合肥善本生物科技有限公司

All Rights Reserved. 皖ICP备2023000814号