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KD-Validated RALY Mouse Oligoclonal Antibody

#65291

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Knockdown Validated
Western blotting analysis using RALY antibody (Cat#65291). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with RALY antibody (Cat#65291, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using RALY antibody (Cat#65291). RALY expression in wild-type (WT) and RALY knockdown (KD) HT-1080 cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with RALY antibody (Cat#65291, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunohistochemistry was performed on paraffin-embedded human gastric carcinoma using RALY antibody (Cat#65291, 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.
Immunocytochemical staining of HepG2 cells with RALY antibody (Cat#65291, 1:1,000). Nuclei were stained blue with DAPI; RALY 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 RALY expression in HepG2 cells using RALY antibody (Cat#65291, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, RALY.
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Unit price:
$89.00
Quantity:
1
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  • Gene Symbol:
    RALY
  • Catalog:
    65291
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H
Information
Product Name KD-Validated RALY Mouse Oligoclonal Antibody
Aliases RALY; RALY Heterogeneous Nuclear Ribonucleoprotein; HNRPCL2; P542; RNA-Binding Protein (Autoantigenic, HnRNP-Associated With Lethal Yellow); HnRNP Associated With Lethal Yellow Protein Homolog; Heterogeneous Nuclear Ribonucleoprotein C-Like 2; HnRNP Core Protein C-Like 2; RNA-Binding Protein Raly; Autoantigen P542; RNA Binding Protein, Autoantigenic (HnRNP-Associated With Lethal Yellow Homolog (Mouse)); RNA Binding Protein, Autoantigenic (HnRNP-Associated With Lethal Yellow Homolog); RNA-Binding Protein (Autoantigenic)
Background

Gene Name: RALY

NCBI Gene Entry: 22913

UniProt Entry: Q9UKM9

Application Information

Molecular Weight: Predicted, 32 kDa; observed, 37 kDa

Clonality: Mouse oligoclonal antibody

Species Reactivity: Human

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC), immunohistochemistry-paraffin (IHC-P)

Immunogen Recombinant protein of human RALY
Isotype Mouse 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): 1:500-1:2,500
Flow Cytometry (FCM): 1:200-1:2,000
Immunocytochemistry (ICC): 1:100-1:1,000
Immunohistochemistry-Paraffin (IHC-P): 1:100-1:200
Note This product is for research use only.
Data
  • Western blotting analysis using RALY antibody (Cat#65291). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with RALY antibody (Cat#65291, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Western blotting analysis using RALY antibody (Cat#65291). RALY expression in wild-type (WT) and RALY knockdown (KD) HT-1080 cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with RALY antibody (Cat#65291, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Immunohistochemistry was performed on paraffin-embedded human gastric carcinoma using RALY antibody (Cat#65291, 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.
  • Immunocytochemical staining of HepG2 cells with RALY antibody (Cat#65291, 1:1,000). Nuclei were stained blue with DAPI; RALY 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 RALY expression in HepG2 cells using RALY antibody (Cat#65291, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, RALY.
Western blotting analysis using RALY antibody (Cat#65291). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with RALY antibody (Cat#65291, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using RALY antibody (Cat#65291). RALY expression in wild-type (WT) and RALY knockdown (KD) HT-1080 cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with RALY antibody (Cat#65291, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunohistochemistry was performed on paraffin-embedded human gastric carcinoma using RALY antibody (Cat#65291, 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.
Immunocytochemical staining of HepG2 cells with RALY antibody (Cat#65291, 1:1,000). Nuclei were stained blue with DAPI; RALY 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 RALY expression in HepG2 cells using RALY antibody (Cat#65291, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, RALY.
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