Anti-CD11b antibody [EP1345Y] - BSA and Azide free

7 product images

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  Image from Sindhu et al PLoS One. 2015 Jul 22;10(7):e0133494. doi: 10.1371/journal.pone.0133494. eCollection 2015. Fig 5.

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  Enhanced expression of monocytes/ macrophage markers in the obese adipose tissue.

  The protein expression (intensity) of monocyte/ macrophage markers was detected by immunohistochemistry (IHC) in the adipose tissue samples from lean, overweight, and obese individuals, 10 each. As shown by representative IHC photomicrographs (100× magnification), expression of (A) CD11b was found to be markedly elevated in overweight and obese adipose tissue samples as compared with lean samples.

  Paraffin-embedded sections (4 μm thick) of subcutaneous adipose tissue were deparaffinized in xylene and rehydrated through descending grades of ethanol (100%, 95%, and 75%) to water. Antigen retrieval was performed under pressure cooker boiling for 8 min and cooling for 15 min. After washing in PBS, endogenous peroxidase activity was blocked with 3% H₂O₂ for 30 min and non-specific antibody binding was clocked with 5% nonfat milk for 1hr and 1% bovine serum albumin (BSA) solution for 1hr. Slides were treated overnight with primary antibodies at room temperature. After washing with PBS (0.5% Tween), slides were incubated for 1hr with secondary antibody conjugated with HRP polymer chain and color was developed using 3,3'-diaminobenzidine chromogen substrate. Specimens were washed in running tap water, lightly counterstained with hematoxylin, dehydrated through ascending grades of ethanol (75%, 95%, and 100%), cleared in xylene, and finally mounted in dibutyl phthalate xylene (DPX).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).

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  Image from Martin et al PLoS One. 2014 Feb 5;9(2):e88226. doi: 10.1371/journal.pone.0088226. eCollection 2014. Fig 6.

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  Duchenne muscular dystrophy (DMD) muscle was co-stained for Neu5Gc (green), Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 (red) and DAPI (blue).

  For double immunostaining, sections were first stained overnight at 4°C with anti-Neu5Gc after blocking in 10% (Neu5Gc-free) human serum, after blocking in 5 mg/mL BSA, sections were incubated overnight with both primary antibodies without fixation, washed for one hour and incubated with the appropriate secondary antibodies.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).

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  Immunoprecipitation - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 (purified) at 1:30 dilution (2 μg) immunoprecipitating CD11b in TF-1 (Human bone marrow erythroleukemia cell line) whole cell lysate.
  Lane 1: TF-1 whole cell lysate 10 μg (input).
  Lane 2: Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 + TF-1 whole cell lysate
  Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 in TF-1 whole cell lysate
  For western blotting, VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used for detection at 1:1000 dilution.
  Blocking and diluting buffer: 5% NFDM/TBST.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).

  All lanes: Immunoprecipitation - Anti-CD11b antibody [EP1345Y] - C-terminal (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478)

  Predicted band size: 127 kDa

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human cervical cancer tissue sections labeling CD11b with purified Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 at 1:1000 dilution (0.28 µg/ml). Heat mediated antigen retrieval was performed using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0) ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Hematoxylin was used as a counterstain.

  Negative control: PBS instead of the primary antibody (inset).

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).

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  Immunocytochemistry/ Immunofluorescence - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  Unpurified Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 staining CD11b in the THP-1 (Human monocytic leukemia cell line) cell line by ICC/IF (Immunocytochemistry/immunofluorescence).

  Cells were fixed with 100% methanol. Samples were incubated with primary antibody (1/250). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 was used as the secondary antibody (1/1000). Nuclei were stained with DAPI.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  Immunohistochemical analysis of paraffin-embedded human spleen tissue using unpurified Anti-CD11b antibody [EP1345Y] - C-terminal ab52478 at a dilution of 1/100.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD11b antibody [EP1345Y] - BSA and Azide free (ab187537)

  This IHC data was generated using the same anti-CD11b antibody clone, EP1345Y, in a different buffer formuatlion (cat# Anti-CD11b antibody [EP1345Y] - C-terminal ab52478).
  

  IHC image of CD11b staining in a formalin fixed, paraffin embedded normal human spleen tissue section*, performed on a Leica Bond™ system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6, epitope retrieval solution 1) for 20 minutes. The section was then incubated with Anti-CD11b antibody [EP1345Y] - C-terminal ab52478, 5 μg/ml, for 15 minutes at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre