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Vectastain abc kit and diaminobenzidine

Manufactured by Vector Laboratories
Sourced in United States

The VECTASTAIN ABC Kit is a reagent system used for the detection of antigens in tissue sections or cell preparations. The kit contains a Biotin-Avidin complex (ABC) that binds to the target antigen, allowing for its visualization through a chromogenic substrate like diaminobenzidine (DAB). DAB is an enzymatic substrate that produces a brown reaction product when oxidized, enabling the visualization of the target antigen.

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2 protocols using vectastain abc kit and diaminobenzidine

1

Histological Analysis of Colon Sections

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Histology and immunohistochemical staining were performed on 5-µm thick formalin-fixed, paraffin-embedded colon sections. Colon sections stained with hematoxylin and eosin (H&E), Periodic acid–Schiff (PAS) stain, and Gram stain. Briefly, sections were deparaffinized, followed by antigen retrieval using the antigen retrieval solution (Agilent Technologies, Santa Clara, CA, U.S.A.). Endogenous peroxidase activity was quenched with 3% H2O2 in PBS. Sections were stained using specific primary antibody (Ki-67, Cell Signaling, Danvers, MA, U.S.A.) and VECTASTAIN ABC Kit and diaminobenzidine (Vector Laboratories, Burlingame, CA, U.S.A.). Counterstaining was performed with hematoxylin and stained sections were visualized by Leica DM550B microscope. Ki-67 immunostaining was quantified by counting Ki-67-positive cells in at least 20 crypts per mouse.
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2

Immunohistochemical Analysis of Colonic Tissue

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Colons were excised and cleaned with phosphate buffered saline followed by fixation in neutral buffered formalin (Thermo Fisher, Waltham, MA, USA). The fixed colon tissues were embedded in paraffin and 5 μm thick sections were sliced and placed on glass microscope slides. Immunohistochemical staining was performed as described previously.8 (link) Briefly, sections were deparaffinized, followed by antigen retrieval using the antigen retrieval solution (Agilent Technologies, Santa Clara, CA, USA). Endogenous peroxidase activity was quenched with 3% H2O2 in phosphate buffered saline for 10 min. Sections were stained using specific primary antibodies and Vectastain ABC kit and diaminobenzidine (Vector Laboratories, Burlingame, CA, USA). Counterstaining was performed with hematoxylin and stained sections were visualized by Leica DM550B microscope. Alternatively, in some experiments, fluorescent dye-labeled secondary antibody was used and sections were visualized by LSM 510 (Zeiss) confocal microscopy.
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