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Antigen retrieval citra solution ph 6

Manufactured by BioGenex

Antigen Retrieval Citra Solution (pH 6) is a laboratory reagent used in the process of antigen retrieval. It is a buffer solution with a pH of 6.0 that is designed to help expose target antigens in fixed tissue samples, enabling subsequent immunodetection procedures.

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2 protocols using antigen retrieval citra solution ph 6

1

Immunohistochemical Analysis of SNRNP200 in ALS

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Paraffin-embedded spinal cord and motor cortex tissue sections from 5 sporadic ALS cases, 2 disease controls (DCs) and 2 non-neurologic diseased controls (NNDCs) were obtained from the Barrow Neurological Institute and Target ALS post-mortem tissue bank cores (subject demographics listed in Table 1). Participants of the post-mortem tissue bank cores provided IRB approved informed consent for the collection of post-mortem tissues. Immunohistochemistry (IHC) was performed as previously described13 (link), 34 . Tissue sections were de-paraffinized and rehydrated, and antigen retrieval was performed using the Antigen Retrieval Citra Solution (pH 6) (BioGenex). Tissues were blocked using Super Block supplemented with Avidin (Vector Labs) and incubated with rabbit anti-SNRNP200 antibody (Sigma) diluted in Super Block supplemented with biotin (Vector Labs) overnight. An anti-rabbit biotinylated IgG secondary antibody (Vector Labs) was subsequently added, and immunostaining was visualized using the Vectastain Elite ABC reagent (Vector Labs) and Vector ImmPACT NovaRED peroxidase substrate kit (Vector Labs). Slides were counterstained with hematoxylin (Sigma). Images were acquired using an Olympus BX40 microscope and a minimum of 11 motor neurons were quantified for each case using Image J34 . Details on antibodies used for IHC are listed in Table S1.
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2

Histological Assessment of Pancreatic Fibrosis

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Masson’s trichrome staining was performed on pancreas tissue sections using a Trichrome Stain kit from Abcam, according to the manufacturer’s protocol. For immunohistochemistry, paraffin-embedded pancreas tissue slides were deparaffinized with xylene and hydrated through a graded alcohol series. Endogenous peroxidase activity was blocked with 3% hydrogen peroxide (Fisher Scientific) for 10 min. Antigen retrieval was performed using Antigen Retrieval Citra Solution pH 6 (BioGenex) in a heat cooker for 30 min, followed by avidin/biotin block (Life Technologies) with 10% goat serum + 1% BSA in phosphate-buffered saline and incubated for 30 min. Primary antibody for alpha-smooth muscle actin (α-SMA, 1:200, Abcam) was incubated overnight. Immunostaining was performed using Super Sensitive IHC Detection Systems (BioGenex). Slides were counterstained with DAB chromagen. Both Masson’s trichrome and α-SMA stained slides were scanned at 20x using an Aperio AT2 slide scanner. Three fields were randomly selected from five pancreas tissue slides in each group, and the percent positively stained area in each field was determined using Image J software.
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