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KD-Validated Anti-G-rich RNA sequence binding factor 1 Rabbit Monoclonal Antibody #63672

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Flow cytometric analysis of G-rich RNA sequence binding factor 1 expression in HepG2 cells using G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:2,000). Green, isotype control; red, G-rich RNA sequence binding factor 1.
Immunocytochemical staining of HepG2 cells with G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:1,000). Nuclei were stained blue with DAPI; G-rich RNA sequence binding factor 1 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-G-rich RNA sequence binding factor 1 antibody (Cat#63672). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 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-GRSF1 antibody (Cat#63672). GRSF1 expression in wild type (WT) and GRSF1 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-GRSF1 antibody (Cat#63672, 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).
Validation of G-rich RNA sequence binding factor 1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:2,000) and analyzed using BD flow cytometer.
Immunocytochemical staining of HeLa cells using anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:1,000), Top panel: wild-type (WT); Bottom panal: G-rich RNA sequence binding factor 1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; G-rich RNA sequence binding factor 1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm.
  • 基因名:
    GRSF1
  • 货号:
    63672
  • 应用:
    WB, FCM, IC
  • 物种反应性:
    H
规格:
20 μL,50 μL,100 μL
价格:
¥ 650.00,¥ 1,350.00,¥ 2,500.00
Information
Product Name KD-Validated Anti-G-rich RNA sequence binding factor 1 Rabbit Monoclonal Antibody
Aliases GRSF1; G-Rich RNA Sequence Binding Factor 1; G-Rich Sequence Factor 1; GRSF-1
Background

Gene Name: GRSF1

NCBI Gene Entry: 2926

UniProt Entry: Q12849

Application Information

Molecular Weight: Predicted, 53 kDa, observed, 53 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB1890

Species Reactivity: Human

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

Immunogen A synthesized peptide derived from human GRSF1
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 G-rich RNA sequence binding factor 1 expression in HepG2 cells using G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:2,000). Green, isotype control; red, G-rich RNA sequence binding factor 1.
  • Immunocytochemical staining of HepG2 cells with G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:1,000). Nuclei were stained blue with DAPI; G-rich RNA sequence binding factor 1 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-G-rich RNA sequence binding factor 1 antibody (Cat#63672). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 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-GRSF1 antibody (Cat#63672). GRSF1 expression in wild type (WT) and GRSF1 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-GRSF1 antibody (Cat#63672, 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).
  • Validation of G-rich RNA sequence binding factor 1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:2,000) and analyzed using BD flow cytometer.
  • Immunocytochemical staining of HeLa cells using anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:1,000), Top panel: wild-type (WT); Bottom panal: G-rich RNA sequence binding factor 1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; G-rich RNA sequence binding factor 1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm.
Citation(0)
Flow cytometric analysis of G-rich RNA sequence binding factor 1 expression in HepG2 cells using G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:2,000). Green, isotype control; red, G-rich RNA sequence binding factor 1.
Immunocytochemical staining of HepG2 cells with G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:1,000). Nuclei were stained blue with DAPI; G-rich RNA sequence binding factor 1 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-G-rich RNA sequence binding factor 1 antibody (Cat#63672). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 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-GRSF1 antibody (Cat#63672). GRSF1 expression in wild type (WT) and GRSF1 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-GRSF1 antibody (Cat#63672, 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).
Validation of G-rich RNA sequence binding factor 1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:2,000) and analyzed using BD flow cytometer.
Immunocytochemical staining of HeLa cells using anti-G-rich RNA sequence binding factor 1 antibody (Cat#63672, 1:1,000), Top panel: wild-type (WT); Bottom panal: G-rich RNA sequence binding factor 1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; G-rich RNA sequence binding factor 1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm.
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