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Alexa fluor 594 conjugated donkey anti rabbit igg h l

Manufactured by Thermo Fisher Scientific

Alexa Fluor 594 conjugated donkey anti-rabbit IgG (H+L) is a secondary antibody used to detect and visualize target proteins recognized by primary rabbit antibodies. The Alexa Fluor 594 dye allows for fluorescence detection of the labeled target.

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2 protocols using alexa fluor 594 conjugated donkey anti rabbit igg h l

1

Immunohistochemical Analysis of 11β-HSD1 in Murine Pancreas

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Paraffin sections of the pancreas taken from 3–5 month old, male MT-IGF and wild-type littermates were dewaxed, rehydrated, and blocked with 10% donkey serum, followed by incubation with rabbit anti-11β-HSD1 antibodies (1:100; H-10 sc-20175, Santa Cruz and ab83522, Abcam, Cambridge, MA) at 4°C overnight. After washing with PBS, sections were independently stained with anti-glucagon (C-18 sc-7779, Santa Cruz) and guinea pig polyclonal anti-insulin (ab7842, Abcam) followed by Alexa Fluor 594 conjugated donkey anti-rabbit IgG (H+L) and Alexa Fluor 488 goat anti-guinea pig IgG (Life technologies, Carlsbad, CA) [14 (link), 15 (link)]. The images were analyzed using Axioshop 2 plus microscope (Carl Zeiss, Jena, Germany), Retiga 1300 digital camera, and Northern Eclipse software (Empix Imaging, Mississauga, ON). Paraffin sections of liver and pancreata taken from 3–5 month old male wild-type mice were incubated overnight with anti-11β-HSD1 (ab83522) with or without a specific blocking peptide (ab99223) at 4°C. After washing, the sections were incubated with secondary antibody and stained with diaminobenzidine substrate (Vector Laboratories). The microscopic images were analyzed using BX61 UIS2 Optical System microscope (Olympus) and Olympus stream software.
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2

Immunofluorescence Staining of CD68 and CLEC4E in Gastric Mucosa

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To confirm whether CLEC4E was expressed in TAMs, double IF staining for CD68 and CLEC4E was performed as previously described [20 ]. The deparaffinized and rehydrated gastric mucosa sections underwent antigen retrieval, and were blocked by 10% bovine serum albumin (BSA) for 1 h at 37 °C. Following this, the sections were incubated with primary antibodies overnight at 4 °C. The primary antibodies used were CD68 (Abcam, ab303565, 1:50) and CLEC4E (Abcam, ab100846, 1:100). Subsequently, Alexa Fluor 594-conjugated donkey anti-rabbit IgG (H + L) (Life Technologies, A21207, 1:400) and Alexa Fluor 488-conjugated donkey anti-mouse IgG (H + L) (Life Technologies, A21202, 1:400) were used as secondary antibodies. The sections were viewed and photographed using a fluorescence microscope (ECLIPSE C1; NIKON, Tokyo, Japan). Six field images per animal were randomly selected to calculate the average number of CD68/CLEC4E-positive cells.
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