Western Blot - Anti-Acetyl Coenzyme A Carboxylase Rabbit mAb [92K41K44]

All lanes: R011403 at 1:2,000 dilution

Lane 1: Hel ( Human erythroLeukemia  suspension cell) whole cell lysates

Lane 2: K562 (Human chronic myeloid leukemia cell) whole cell lysates

Lane 3: U87 (Human malignant glioblastoma epithelial cells) whole cell lysates

Lysates/proteins at 10 µg per lane.

Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP Conjugated (Cat. No. LF102) at 1:5,000 dilution

Predicted band size: 277 kDa

Observed band size: 277 kDa

Developed using the ECL technique (Cat. No. SQ201).

Immunofluorescence - Anti-Acetyl Coenzyme A Carboxylase Rabbit mAb [92K41K44]

Sample: HeLa cells

The cells were fixed with 4% paraformaldehyde (10 min), permeabilized with 0.5% Triton X-100 for 10 minutes and then blocked with 5% BSA in 0.1% PBS-Tween for 0.5 hours.

Primary antibodies: R011403 at 1:100 dilution and α-tubulin Mouse Monoclonal Antibody (Cat. No. LF209) at 1:100 dilution

Secondary antibodies: Goat anti-Rabbit (488) at 1:1,000 dilution (shown in green) and Goat anti-Mouse (555) at 1:1,000 dilution (shown in red)

Nuclei were stained with DAPI (shown in blue).

Immunohistochemistry - Anti-Acetyl Coenzyme A Carboxylase Rabbit mAb [92K41K44]

Sample: Paraformaldehyde-fixed, paraffin embedded human breast cancer tissue

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 30 mins.

Primary antibody: R011403 at 1:200 dilution

Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP conjugated at 1:1,000 dilution

DAB was used as the chromogen.

Counter stained with hematoxylin.

Positive/negative staining were presented.

Only the secondary antibody was used as the negative control.

Immunohistochemistry - Anti-Acetyl Coenzyme A Carboxylase Rabbit mAb [92K41K44]

Sample: Paraformaldehyde-fixed, paraffin embedded human gastric cancera tissue

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 30 mins.

Primary antibody: R011403 at 1:200 dilution

Secondary antibody: Goat Anti-Rabbit IgG (H+L), HRP conjugated at 1:1,000 dilution

DAB was used as the chromogen.

Counter stained with hematoxylin.

Positive/negative staining were presented.

Only the secondary antibody was used as the negative control.