Anti-Fibronectin antibody [F1] - BSA and Azide free

3 product images

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Fibronectin antibody [F1] - BSA and Azide free (ab271831)

  Immunohistochemical staining of paraffin embedded human breast carcinoma with purified Anti-Fibronectin antibody [F1] ab32419 at a dilution of 1/250. The secondary antibody used is Goat Anti-Rabbit IgG H&L (HRP) ab97051, a HRP-conjugated goat anti-rabbit IgG (H+L), at a dilution of 1/500. The sample is counter-stained with hematoxylin. Antigen retrieval was perfomed using Tris-EDTA buffer, pH 9.0. PBS was used instead of the primary antibody as the negative control, and is shown in the inset.

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Fibronectin antibody [F1] ab32419).

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  Flow Cytometry (Intracellular) - Anti-Fibronectin antibody [F1] - BSA and Azide free (ab271831)

  Intracellular Flow Cytometry analysis of HepG2 (Human liver hepatocellular carcinoma cell line) cells labeling Fibronectin with purified Anti-Fibronectin antibody [F1] ab32419 at 1/20 dilution (10 μg/mL) (red). Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. A Goat anti rabbit IgG (Alexa Fluor^®488) at 1/2000 dilution was used as the secondary antibody. Rabbit monoclonal IgG (Black) was used as the isotype control, cells without incubation with primary antibody and secondary antibody (Blue) was used as the unlabeled control.
  

  This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Fibronectin antibody [F1] ab32419).

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  Immunocytochemistry/ Immunofluorescence - Anti-Fibronectin antibody [F1] - BSA and Azide free (ab271831)

  ICC/IF image of unpurified Anti-Fibronectin antibody [F1] ab32419 stained HepG2 (Human liver hepatocellular carcinoma cell line) cells. The cells were fixed in 4% formaldehyde (10 minutes) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1 hour to permeabilize the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody Anti-Fibronectin antibody [F1] ab32419 at 1/100 dilution overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti- rabbit (Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899) IgG (H+L) used at a 1/1000 dilution for 1 hour. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1 hour. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43 µM.
  Alexa Fluor® 488 (Alexa Fluor® 488 Anti-Fibronectin antibody [F1] ab198933) and Alexa Fluor® 647 (Alexa Fluor® 647 Anti-Fibronectin antibody [F1] ab198934) conjugated versions are available for this clone.This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (Anti-Fibronectin antibody [F1] ab32419).