Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free

10 product images

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  Immunohistochemistry (Frozen sections) - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  Immunohistochemical analysis of 4% paraformaldehyde-fixed, 0.2% Triton X-100-permeabilised mouse cerebrum tissue staining glutamine synthetase with Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 at 1/250 dilution, followed by alexaFluor®488 Goat anti-Rabbit secondary (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/1000 dilution. Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20). DAPI was used as a nuclear counterstain.
  

  Positive staining on mouse cerebrum (PMID: 23895693).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562).

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  Western blot - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  This data was developed using Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562, the same antibody clone in a different buffer formulation.
  

  Blocking and diluting buffer: 5% NFDM/TBST

  All lanes: Western blot - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193) at 1/2000 dilution

  Lane 1: Human fetal liver lysates at 20 µg

  Lane 2: HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 15 µg

  Lane 3: Mouse spleen lysates at 20 µg

  Lane 4: Rat spleen lysates at 20 µg

  Secondary

  All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

  Predicted band size: 42 kDa

  Observed band size: 42 kDa

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  Western blot - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  This data was developed using Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562, the same antibody clone in a different buffer formulation.

  All lanes: Western blot - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193) at 1/1000 dilution

  Lane 1: Human fetal liver lysate at 10 µg

  Lane 2: Jurkat cell lysate at 10 µg

  Lane 3: HeLa cell lysate at 10 µg

  Developed using the ECL technique.

  Predicted band size: 42 kDa

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  Western blot - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  This data was developed using Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562, the same antibody clone in a different buffer formulation:
  

  Lanes 1 - 2: Merged signal (red and green). Green - Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 observed at 42 kDa. Red - loading control, Anti-Vinculin antibody [VIN-54] ab130007, observed at 130 kDa.

  Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 was shown to recognize Glutamine Synthetase in wild-type HAP1 cells as signal was lost at the expected MW in GLUL knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and GLUL knockout samples were subjected to SDS-PAGE. Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 and Anti-Vinculin antibody [VIN-54] ab130007 (Mouse anti-Vinculin loading control) were incubated overnight at 4°C at 1 μg/ml and 1/20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye^® 800CW) preabsorbed Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye^® 680RD) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.

  All lanes: Western blot - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193) at 1 µg

  Lane 1: Wild-type HAP1 whole cell lysate at 20 µg

  Lane 2: GLUL knockout HAP1 whole cell lysate at 20 µg

  Predicted band size: 42 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  Immunohistochemical analysis of formalin-fixed, paraffin-embedded, Human glioma tissue labeling Glutamine Synthetase with unpurified Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 at a 1/100 dilution.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562).

  Heat mediated antigen retrieval was performed with citrate buffer pH 6 before commencing with IHC staining protocol.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human glioma tissue sections labeling Glutamine Synthetase with purified Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 at 1:500 dilution (0.18 μg/ml). Heat mediated antigen retrieval was performed using citrate Buffer, pH6.0. Tissue was counterstained with Hematoxylin. ImmunoHistoProbe one step HRP Polymer (ready to use) secondary antibody was used at 1:0 dilution. PBS instead of the primary antibody was used as the negative control.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562).

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  Immunohistochemistry (Frozen sections) - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  Immunohistochemical analysis of 4% paraformaldehyde-fixed, 0.2% Triton X-100-permeabilised rat cerebrum tissue staining glutamine synthetase with Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 at 1/250 dilution, followed by alexaFluor®488 Goat anti-Rabbit secondary (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) at 1/1000 dilution. Heat mediated antigen retrieval was performed using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20). DAPI was used as a nuclear counterstain.
  

  Positive staining on rat cerebrum (PMID: 23895693).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  Immunohistochemical analysis of formalin-fixed, paraffin-embedded, Human liver tissue labeling Glutamine Synthetase with unpurified Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 at a 1/100 dilution.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562).

  Heat mediated antigen retrieval was performed with citrate buffer pH 6 before commencing with IHC staining protocol.

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  This image is courtesy of Alex Van Engelenburg

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562 staining Glutamine Synthetasein Mouse Liver tissue sections by Immunohistochemistry (PFA perfusion fixed frozen sections). Tissue samples were fixed by perfusion with formaldehyde, blocked with PB Protein Block ab64226 for 10 minutes at room temperature and antigen retrieval was by heat mediation in citrate buffer. The sample was incubated with primary antibody (1/200) for 30 minutes. A HRP-conjugated Goat anti-rabbit polyclonal (1/200) was used as the secondary antibody.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562).

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  Multiplex immunohistochemistry - Anti-Glutamine Synthetase antibody [EPR13022(B)] - BSA and Azide free (ab240193)

  This data was developed using Anti-Glutamine Synthetase antibody [EPR13022(B)] ab176562, the same antibody clone in a different buffer formulation.
  
  Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Human retina tissue labeling PAX6, Glutamine Synthetase and CRX with Anti-PAX6 antibody [EPR3352(2)] ab109233 at 1/10000 dilution, ab240193 at 1/20000 dilution and Anti-CRX antibody [EPR9582] - BSA and Azide free ab248897 at 1/1000 dilution followed by a ready to use Opal Polymer HRP Ms + Rb secondary antibody. Nuclear counter stain used was DAPI.
  
  Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
  
  Panel A: merged staining of anti-CRX (gray; Opal™690), anti-Glutamine Synthetase (green; Opal™520) and anti-PAX6 (red; Opal™570) on human retina.
  Panel B: anti-PAX6 stained on retinal progenitor cells.
  Panel C: anti-Glutamine Synthetase stained on Müller glia.
  Panel D: anti-CRX stained on subset cells of outer nuclear layer and inner nuclear layer.
  
  The section was incubated in three rounds of staining: in the order of Anti-CRX antibody [EPR9582] - BSA and Azide free ab248897, ab240193, and Anti-PAX6 antibody [EPR3352(2)] ab109233 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
  
  The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.