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KD-Validated Anti-GCLM Recombinant Rabbit Monoclonal Antibody #62007

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Flow cytometric analysis of GCLM expression in HepG2 cells using GCLM antibody (Cat#62007, 1:2,000). Green, isotype control; red, GCLM.
Immunocytochemical staining of HepG2 cells with anti-GCLM antibody (Cat#62007, 1:1,000). Nuclei were stained blue with DAPI; GCLM 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-GCLM antibody (Cat#62007). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-GCLM antibody (Cat#62007, 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-GCLM antibody (Cat#62007). GCLM expression in wild type (WT) and GCLM shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with anti-GCLM antibody (Cat#62007, 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 GCLM knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-GCLM antibody (Cat#62007, 1:2,000) and analyzed using BD flow cytometer.
  • 基因名:
    GCLM
  • 货号:
    62007
  • 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-GCLM Recombinant Rabbit Monoclonal Antibody
Aliases GCLM; Glutamate-Cysteine Ligase Modifier Subunit; GLCLR; Gamma-Glutamylcysteine Synthetase Regulatory Subunit; Glutamate--Cysteine Ligase Regulatory Subunit; Gamma-ECS Regulatory Subunit; GCS Light Chain; Glutamate-Cysteine Ligase (Gamma-Glutamylcysteine Synthetase), Regulatory (30.8kD); Glutamate-Cysteine Ligase Modifier Subunit Delta2 Alternative Splicing; Glutamate-Cysteine Ligase Regulatory Protein; Glutamate-Cysteine Ligase, Modifier Subunit; Glutamate--Cysteine Ligase Modifier Subunit; Gamma-Glutamylcysteine Synthetase; GSC Light Chain
Background

Gene Name: GCLM

NCBI Gene Entry: 2730

UniProt Entry: P48507

Application Information

Molecular Weight: Predicted, 31 kDa, observed, 28 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB5535

Species Reactivity: Human, mouse, rat

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

Immunogen A synthesized peptide derived from human GCLM
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.
Data
  • Flow cytometric analysis of GCLM expression in HepG2 cells using GCLM antibody (Cat#62007, 1:2,000). Green, isotype control; red, GCLM.
  • Immunocytochemical staining of HepG2 cells with anti-GCLM antibody (Cat#62007, 1:1,000). Nuclei were stained blue with DAPI; GCLM 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-GCLM antibody (Cat#62007). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-GCLM antibody (Cat#62007, 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-GCLM antibody (Cat#62007). GCLM expression in wild type (WT) and GCLM shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with anti-GCLM antibody (Cat#62007, 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 GCLM knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-GCLM antibody (Cat#62007, 1:2,000) and analyzed using BD flow cytometer.
Flow cytometric analysis of GCLM expression in HepG2 cells using GCLM antibody (Cat#62007, 1:2,000). Green, isotype control; red, GCLM.
Immunocytochemical staining of HepG2 cells with anti-GCLM antibody (Cat#62007, 1:1,000). Nuclei were stained blue with DAPI; GCLM 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-GCLM antibody (Cat#62007). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-GCLM antibody (Cat#62007, 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-GCLM antibody (Cat#62007). GCLM expression in wild type (WT) and GCLM shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with anti-GCLM antibody (Cat#62007, 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 GCLM knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-GCLM antibody (Cat#62007, 1:2,000) and analyzed using BD flow cytometer.
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